3770 Sampling Jobs - Page 28

Hi! We're Charcoal. The world is filled with primitive, dull products that don’t add much value to our lives. A desk is just a surface to hold things up or an article of clothing is just a surface on our skin. We're changing that by leveraging great design and engineering to unlock the potential of everyday products that have remained stagnant for centuries. Check out our products here - www.charcoal.inc ROLE - Senior Industrial/Product Designer Key Responsibilities: Lead the industrial design process : research, concept generation, prototyping, refinement, CMF, and DFM (Design for Manufacturing) Create 3D CAD models, detailed drawings, and high-quality renderings for marketing and manufacturing Collaborate with mechanical engineers to ensure designs are feasible, manufacturable, and aligned with cost and tooling constraints. Own the CMF (Color, Material, Finish) direction and coordinate with suppliers for sampling and final production validation. Develop physical prototypes (mock-ups, 3D prints, soft models ) to validate form, ergonomics, and user interaction. Participate in user research, competitive benchmarking, and trend analysis to inform design decisions. Contribute to packaging, accessory, and product ecosystem design where needed. Required Skills & Qualifications: 3–5 years of experience in Industrial Design, preferably in consumer products, lifestyle products, hardware startups, or design consultancies. Expert-level proficiency in industrial design software , including: 1) 3D Modeling : Rhino / Fusion 360 2) Rendering : KeyShot / Blender / V-Ray 3) 2D : Adobe Creative Suite (Illustrator, Photoshop, InDesign) Strong knowledge of materials, manufacturing processes, and prototyping (plastics, metals, soft goods, sheet metal, CNC, 3D printing). Exceptional sketching, storytelling, and visual communication skills. Understanding of ergonomics, human factors, and user-centered design . Portfolio that demonstrates real, shipped products —not just concept work. Ability to work in a lean, ambiguous, startup environment where ownership and resourcefulness are valued over titles and process. Bonus: Experience with soft goods, CMF libraries, packaging, or branding design. What We’re Looking For: A builder mindset—someone who can think, design, prototype, and ship. Hands-on attitude: You should be comfortable opening CAD files, sending things for prototyping, and tweaking renders yourself. Attention to detail and taste —you care about the final product in the user’s hands. Collaborative but independent —you know when to push for quality and when to ship fast. Eager to grow with the company and build design culture from the ground up. Why Join Us? Work directly with founders and core team. Freedom to design products that are distinctive, thoughtful, and real. Opportunity to help define the physical identity of an emerging brand. Rapid prototyping and direct-to-market execution cycles , not endless presentations. Be part of a hands-on, no-nonsense product team that ships.

This job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Use Your Power for Purpose Every day, Pfizer's unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients. What You Will Achieve In this role, you will: Evaluate and review clinical and commercial drug batches to ensure compliance with established specifications. Conduct rigorous sampling and statistical process control procedures to identify deviations from standards. Approve investigations and change control activities to maintain compliance with configuration management policies. Contribute to moderately complex projects, managing time effectively and developing short-term work plans. Independently assess Change Control activities for potential Quality and Operational Good Manufacturing Practices (cGMP) impacts. Investigate and document Quality Assurance deviations, escalating issues to the Quality Assurance Lead as needed. Ensure regulatory compliance with current Good Manufacturing Practices (GxP) and provide Quality Review and oversight of site documentation to meet global regulatory and Pfizer quality standards. Here Is What You Need (Minimum Requirements) High school diploma (or equivalent) with 8+ years of experience or associate's degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience Solid understanding of current Good Manufacturing Practices and relevant GxP regulations and standards Strong critical thinking skills Ability to work effectively within own team and interdepartmental teams Good working knowledge of Microsoft Excel and Word Proactive approach to problem-solving Bonus Points If You Have (Preferred Requirements) Experience in quality administered systems Strong organizational skills and attention to detail Experience with regulatory compliance and documentation Ability to mentor and review the work of other colleagues Preferred Education/ Qualification B.Pharm/ M.Pharm/ M.S (Pharmacy)/ M.Sc/ BE Experience 6+ years of experience in validation function of sterile dosage form facility. Core Competencies Understanding of pharmaceutical manufacturing, packaging, quality assurance, and quality control operations. Knowledge of validation principles and practices related to the following areas: manufacturing process, analytical method, cleaning methods, facility, equipment, instrument, utility system, and CSV systems. Conversant with design & working principles of key equipment used in sterile manufacturing -Autoclave, Vial washing, Heat tunnel, Homogenizers, Vail filling, Filter integrity testing devices, Visual inspection equipment, Packing equipment, and Cleaning Validations. Well versed with Terminal process - design, execution and review. Experience in plant and TS operations. Good document review skills, data analysis with ability to identify issues and recommend actions Knowledge on the Qualification instruments and Tools. Knowledge on the GAMP requirements, PDA guidance, ISO guideline, 21 CFR part 11. Knowledge on the Components level assessment, PM requirement. Good knowledge on the Validation instruments calibration. Knowledge on the assessment of the Change controls and failure investigations. Knowledge of current validation regulations in the industry and validation principles. cGMPs and FDA regulatory guidelines. Strong Technical skills, leadership, organizational planning and project management skills, in addition to strong technical background required to coordinate multi-disciplinary teams. Strong interpersonal skills. Excellent interpersonal effectiveness and communication skills (written and oral) to interface across departments and management levels. Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control

Quality Coordination Ensure all materials, components, and final products meet regulatory and buyer-specific quality standards. Perform regular inspections on production floors including inline, midline, and final inspections based on AQL standards. Assess product samples and components for consistency, craftsmanship, and finish levels before approvals. Identify and promptly resolve any production or quality-related discrepancies, working closely with suppliers and internal teams. Monitor vendor performance and participate in quarterly evaluations to ensure continual improvement. Maintain documentation related to quality checks, vendor audits, and inspection reports for management reference. Collaborate closely with the Product Line, Sales, and Operations teams to ensure timely and successful execution of sampling and bulk orders. Skills: inspection techniques,quality assurance,documentation,quality assurance processes,supply chain,collaboration,regulatory standards,vendor management,vendor negotiation,english

Job Title: Apparel Production & Buying Head – Women’s Wear (Tops & Bottoms) Location: Ambernath, Maharashtra Type: Full-Time Experience Required: 2+ years in women’s wear buying & production coordination (Dmart, Zudio, Westside, etc. preferred) ⸻ Job Description: We’re hiring a hands-on, multi-talented individual to lead our women’s wear vertical (tops & bottoms) — someone who can bridge the gap between design, production, and purchase teams, while actively building partnerships with retail chains. ⸻ Key Responsibilities: • Oversee the entire production lifecycle: from sample development to bulk delivery. • Work with in-house designers and ensure styles are market-relevant, trend-forward, and cost-efficient. • Manage sourcing, sampling, fabric selection, trims, and vendor coordination. • Establish tie-ups with corporate purchase departments (Zudio, Westside, Dmart, etc.). • Coordinate between internal design and production teams for timely execution. • Monitor quality, costing, and lead times to ensure profitable output. ⸻ Requirements: • 2+ years of experience in women’s fashion (tops & bottoms) – buying, production, or merchandising. • Must have exposure to value retail or mass-market category. • Strong vendor network and negotiation skills. • Ability to handle multi-department coordination. • Based in or willing to relocate to Ambernath. ⸻ To Apply: Email your CV to gaurav.j.phagwani@gmail.com or DM directly.

Position Summary: We are seeking a Sustainability Intelligence Officer to lead the development of our new sustainability Intelligence platform. This role is responsible for integrating sustainability into the core of our market research business — driving ESG-related insights, sustainable research practices, and building sustainability intelligence capabilities that can be leveraged across client-facing research, analytics, and consulting services. Key Responsibilities: · Develop and implement the strategic vision and operational plan for the sustainability intelligence platform. Research about sustainability policies and frameworks aligned with global best practices. Build partnerships with sustainability experts, research vendors, and data platforms. Identify potential service offerings such as ESG trend reports, consumer perception analysis, or impact measurement tools. Conduct sustainability intelligence gathering — tracking ESG trends, policy shifts, consumer attitudes, and emerging technologies. Integrate sustainability metrics into existing research products, surveys, and analytics tools. Develop proprietary sustainability indices, benchmarks, or impact scoring systems relevant to client sectors. Guide research teams on sustainable data collection methods (e.g., ethical sampling, responsible AI). Support sustainability-related client consulting projects, whitepapers, and thought leadership. Qualifications: Bachelor's or Master's degree in Sustainability, Environmental Science, Market Research, Economics, or a related field. 8–10 years of experience in ESG strategy, sustainability analytics, or market research roles. Strong understanding of ESG reporting frameworks and sustainability rating systems. Experience conducting or interpreting quantitative and qualitative research in a commercial context. Strong communication and stakeholder engagement skills — able to influence across levels. Desirable Skills: Familiarity with market research methodologies (quantitative and qualitative). Experience using data analytics or visualization tools (e.g., SPSS, Power BI, Tableau). Knowledge of sustainable product development, responsible marketing, or consumer trends related to ESG. Certifications in sustainability (e.g., ISSP-SA, LEED, GRI, CFA ESG). What We Offer: Opportunity to lead a transformative function within a forward-thinking market research organization. Autonomy to design new research offerings at the intersection of sustainability and business insights. Access to an entrepreneurial environment with cross-functional collaboration. Competitive compensation, flexible work arrangements, and career growth potential. We are open for Ahmedabad / Mumbai, India.

Position: Executive / Senior Executive – Quality Control (QC) Experience: 1–2 years | 2–3 years | 4–5 years Qualification: B.Sc / B.Pharm / M.Sc / M.Pharm Industry Preferred: Cosmetics / Pharmaceuticals / FMCG Overview: The Quality Control (QC) Executive / Senior Executive will be responsible for ensuring that products consistently meet the company’s defined quality standards through systematic sampling, testing, inspections, and documentation. The role also supports compliance with regulatory norms and continuous improvement of quality processes. Responsibilities: Conduct quality testing of raw materials, in-process, and finished products as per SOPs. Identify, document, and escalate any non-conformities or deviations found during testing. Maintain thorough and accurate records of test results, logs, and batch documents. Ensure alignment with GMP, GLP, and applicable regulatory requirements. Coordinate with the production team to troubleshoot and resolve quality-related concerns. Prepare and assist in internal and external audits and regulatory inspections. Monitor key quality metrics and provide inputs for process improvements. Skills Required: Experience ranging from 2 to 5 years in QC roles within cosmetic, pharma, or FMCG industries. Strong technical understanding of quality control protocols, lab equipment, and analytical techniques. Knowledge of regulatory frameworks like ISO, WHO-GMP, FDA, etc. Detail-oriented mindset with strong documentation and analytical skills. Proficiency in handling quality management systems (QMS) and MS Office. Effective communication and interpersonal abilities.

About Us Welcome to Swiss Beauty, the fastest-growing beauty and cosmetics brand in India. Established in 2013, Swiss Beauty aims to be the ultimate companion and BFF of every makeup lover, transforming beauty routines into extraordinary experiences. With a focus on Indian beauty needs, we merge global cosmetic standards with our expertise to create highly innovative, long-lasting, and comfortable products. Our mission is to elevate beauty to Swiss standards and offer game-changing products that set new benchmarks in the industry. We believe that makeup knows no boundaries and is for everyone. Join us on this remarkable journey as we redefine beauty norms and celebrate individuality. About The Role We are seeking a creative and detail-oriented Packaging Design Intern to support our in-house design team in crafting innovative, functional, and aesthetically aligned packaging for our beauty product portfolio. This internship is ideal for someone passionate about product aesthetics, structural design, and brand storytelling through packaging. You’ll gain hands-on exposure to the complete packaging design lifecycle—from concept to production—while contributing to real-world product launches and design systems across categories. Key Responsibilities Assist in designing primary and secondary packaging: unit cartons, tubes, bottles, labels, outer boxes Support KLD (Key Line Drawing) creation, structural mockups, dielines, and final production-ready artworks Adapt master design templates across multiple SKUs, formats, and sizes Collaborate with product, brand, marketing, and external vendors to ensure alignment on packaging needs Ensure all designs adhere to brand guidelines, compliance standards, and print production specs Stay updated with trends in packaging, sustainability, and innovations in materials or formats Support coordination for vendor proofing, color matching, and sampling processes What We’re Looking For Students or recent graduates in Graphic Design, Packaging Design, Industrial Design, or related disciplines Proficiency in Adobe Illustrator, Photoshop, and InDesign Bonus: Working knowledge of 3D design tools like Adobe Dimension, Blender, or Esko Strong sense of typography, visual hierarchy, layout, and brand alignment Basic understanding of printing processes, materials, and packaging finishes A team player with excellent attention to detail and the ability to adapt quickly to feedback Passion for the beauty industry, aesthetics, and packaging innovation What You’ll Gain Mentorship from an experienced and collaborative design team First-hand experience in live packaging design projects and product development timelines Understanding of print production, material sourcing, and packaging compliance Portfolio-worthy projects and creative contributions to real brand launches Exposure to a dynamic, fast-paced beauty & D2C environment While this internship is for a fixed period, outstanding interns may be considered for full-time positions based on performance and availability or the requirements within the company. We encourage you to demonstrate your skills and dedication throughout your time with us. Note: This is a paid internship.Skills: indesign,aesthetics,photoshop,layout,launches,3d design tools,packaging design,visual hierarchy,typography,adobe illustrator,packaging innovation,design,packaging,adobe

Job Title: Quality Coordinator – Sourcing & NPD Location: Lajpat Nagar, Moradabad, Delhi Industry: Furniture, Home Décor, Manufacturing Job Type: Full-Time | On-site Salary: ₹40,000 to ₹50,000 per month Experience: 5–7 Years (Sourcing, Quality Assurance, Procurement) Education: Bachelor’s degree in Business, Supply Chain, or related field Position Overview We are seeking a dynamic and experienced Quality Coordinator – Sourcing & NPD to manage and elevate our procurement , product development , and quality assurance processes. This role is pivotal in ensuring that all materials, components, and final products meet the highest standards of compliance, consistency, and performance across our furniture and home category . The ideal candidate will be highly detail-oriented, self-motivated, and capable of managing end-to-end sourcing while actively supporting trend-driven new product initiatives and overseeing quality from concept to completion. Key ResponsibilitiesQuality Coordination Ensure all materials, components, and final products meet regulatory and buyer-specific quality standards. Perform regular inspections on production floors including inline, midline, and final inspections based on AQL standards. Assess product samples and components for consistency, craftsmanship, and finish levels before approvals. Identify and promptly resolve any production or quality-related discrepancies, working closely with suppliers and internal teams. Monitor vendor performance and participate in quarterly evaluations to ensure continual improvement. Maintain documentation related to quality checks, vendor audits, and inspection reports for management reference. Collaborate closely with the Product Line, Sales, and Operations teams to ensure timely and successful execution of sampling and bulk orders. Sourcing & Procurement Manage procurement activities across multiple product categories, with a focus on furniture and home décor. Develop and implement a direct factory sourcing strategy to enhance transparency, pricing, and control. Negotiate commercial terms with vendors including pricing, lead times, payment terms, and production capacities. Conduct cost and quality assurance analysis on key items to drive value-based decisions. Work collaboratively with vendors to optimize ranges, improve margin, and mitigate commercial, operational, and contractual risks. Maintain daily updates and communications with local and offshore vendors to ensure smooth operations. New Product Development (NPD) Research and onboard new suppliers using platforms like Alibaba, India Mart, and AliExpress to support NPD initiatives. Coordinate with the HK, Holland, and USA marketing teams to tailor product selections based on trends and seasonal demand. Manage sampling programs end-to-end, including vendor coordination, shipping, and reporting to the Head Office. Create and manage offering and quotation files, including comparison sheets to support sourcing decisions. Maintain accurate databases in Excel for vendor tracking, sample status, pricing, and development stages. Support curated item development based on buyer feedback and market direction. Key Requirements Bachelor’s degree in Business, Supply Chain, or a related field. 5–7 years of experience in sourcing, procurement, buying, and quality assurance within the furniture or home category. Prior experience in buying and vendor negotiations is essential. Experience working with global suppliers is highly desirable. Deep understanding of product materials, manufacturing processes, and inspection standards. Familiarity with global procurement networks and direct factory sourcing. Proven ability to manage cross-functional teams and develop long-term supplier partnerships. Excellent negotiation, problem-solving, and decision-making skills. Highly organized, detail-oriented, and capable of managing multiple concurrent projects. Strong command of Microsoft Excel and documentation practices. Good spoken and written English skills with the ability to handle basic business communication confidently. Relevant Keywords Furniture sourcing jobs, procurement coordinator, home décor quality control, product development jobs, AQL inspection jobs, Moradabad sourcing jobs, vendor management, NPD coordinator jobs, manufacturing quality assurance, factory sourcing Skills: factory sourcing,sourcing,quality assurance,supply chain,compliance,product development,components,procurement,vendor management,audit,negotiation,bulk order,microsoft excel,sales margin,quality assurance processes,sampling,modern furniture,quality check,problem-solving,production,sales,building business partnerships,sourcing materials,performance analysis,teams,inspection standards,quality assurance review,operations,finished goods,strategy,home decor,vendor negotiation,new product ideas,excel,new product development,margin,product sales,tracking budget expenses,quality control,materials,e-commerce,furniture,pricing,manufacturing,tracking,consistency

To provide support for execution and monitoring of trial, scale up, exhibit process qualification batches. To prepare and review new product documents like material requirement sheet, master formula card, bill of material, master formula, risk assessment reports sampling protocol, reports, exhibit batch manufacturing record and exhibit protocols and reports etc. To prepare and review new product documents like sampling protocol and trial batch reports investigation report/Justification report, additional activity protocol, regulatory evaluation etc. To Provide the regulatory response. To share process knowledge to cross functional departments through presentation for smooth technology transfer To prepare and review investigation report/Justification report, additional activity protocol, regulatory evaluation etc. To review and evaluate product history and process parameters for technical remediation and improvement of product robustness. To prepare and submit the investigation reports for OOS, OOT and any failure for exhibit/validation/commercial batch manufacturing and during stability testing. Track wise related activities Change control/CAPA/Planned deviations/Unplanned deviations related activities etc. To prepare and review product containment approach and risk assessment for new product. To prepare and review risk assessment report for elemental impurities/Nitrosamine impurities/residual solvent. To arrange placebo for quality control testing, change part development and to evaluate feasibility of product etc. To prepare and review statistical evaluation for process evaluation. To prepare and review standard operating procedures, training schedule, and conduct training To participate in various regulatory audits to support the plant.

Job Description Position: QA Sterile Manager Department: Quality Assurance Designation: Manager - I Education Qualification: M.Sc. in Biotechnology / Microbiology / Chemistry Total years of Experience: 10+ Years Job Role: Management of Quality Assurance functions of Manufacturing Block – P. Responsibilities Ensure that manufacturing and packing of the batch is executed and records are completed and reviewed in accordance with established SOPs and cGMP regulations. Conduct certification of batch production records for compliance and stage-wise completion. To release / reject the Batch after complete review of batch and related quality documentation. Tracking and monitoring of QMS system. Ensure logical closure of deviations and investigations of related product before release. Conduct thorough investigations along with production for any complaints / deviations/ OOS / stability failure for products manufactured at the site and logical / timely closure of Complaints. To ensure contamination controls implemented and followed at site as per contamination controls strategy (CCS) and respective procedures. Work directly with planning, QC, other QA functions, and Regulatory Affairs to ensure Batches are released to meet supply chain requirements. Participate in self-audits of facility and equipment in partnership with Manufacturing and Engineering to ensure readiness for operations. Participate in Aseptic simulation (Media Fill) activity, Monitoring and Implementation for PENEM DF. Identify continuous improvement opportunities to improve compliance, process clarity, and operational efficiency. Review and approve master batch production records (Manufacturing / packing) and SOPs. Review and approve equipment qualification & process validation protocols and reports for accuracy, completeness, and traceability as well as adherence to protocol / procedures. Review and approve Annual Product Review (APR) reports for the products as per the schedule. Stability sample management of finished goods. Management of control sample pertaining to collection, review, storage and destruction. Management of line clearance, in-process check, coding approval and water sampling. Review and approval of IPQA instrument calibration record. Management of IPQA activities for Block-Penem. Review and approve artwork of Packaging material, STP and Specification. Provides appropriate training and development to support staff to meet their respective job responsibilities. Work in partnership with Manufacturing, Engineering, and QC to increase knowledge and understanding of cGMPs and improve practices and procedures. Review activities related to the Microbiology Laboratory. Review activities related to the beta-lactam containment monitoring. Compliance with Quality Policy of the organization. Improvement of System and procedures, Quality of products manufactured and delivered.

Job Description Position : Microbiology Head Reports to: Quality Head Department: Quality Grade: G8 Functional Area: QC - Microbiology Location: Dewas Position Summary Manage overall site microbiology department wrt sampling, testing, planning, qualifications, media fill program ( for sterile manufacturing),compliance and upgrades of facilities and procedures. Conduct effective review of team and portfolio, provide direction and guidance to the team and develop team competence with the objective of ensuring the quality of products released with adherence to GMP norms and timelines The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, Standard and Procedures. Key Responsibilities Provide leadership and direction to achieve all quality goals. Manage & Organize timely microbiological sampling, testing and release of raw materials, finished product, commercial stability, Exhibit stability, miscellaneous samples. Manage & Organize timely Microbiological sampling, testing and release of water and Utility samples. Manage & Organize timely Microbial Environmental Monitoring of passive air/active air/ Compressed air/equipment surfaces /personnel monitoring & Drain points of manufacturing blocks, warehouses & Microbiology lab etc. Monitoring effectiveness of the disinfectants used at the site and make appropriate timely change to the ineffective proved disinfectants. Manage & Organize timely handling & maintenance of microbial cultures. Isolation & identification of microbial isolates from various sources. Manage & Organize timely laboratory investigation of out of specification results /Out of trends/Out of limit, root cause analysis and Risk assessment and Health hazard evaluation of identified microorganisms. Participate in internal, external and/or regulatory inspections of Microbiology operations at the site. Learn from external regulatory audit observations and implement Global CAPA and local CQA observations CAPA in micro lab Ensure trend and annual summary reports of water/microbial environmental monitoring/Microbial isolates etc. Ensure calibration, validation and qualification of laboratory equipment/instrument. Ensure timely availability of laboratory Chemicals, media/ stationary/ gloves and Consumable. Ensure consistency in Microbiology lab operations and drive continuous improvements in laboratory performance. Ensure compliance to cGMPs and applicable safety standards in the Microbiology laboratory. Train microbiologist about the microbiological techniques, aseptic practices, critical quality management skills, including decision-making, handling of quality exceptions, staff development, personnel and planning, etc. Managing people on a day-do-day basis. Preparation of annual capex & revenue budget for microbiology section. Ensure adherence to approved budget work plan. Oversee that the cost of testing is controlled in microbiology lab. Liaison with Corporate Micro team to implement microbial risk assessment program and work to mitigate effective CAPA’s to prevent failures. Minimum Education/Experience Requirements Microbiology Graduateor Equivalent Minimum 15years With Microbiology Work Experience Preferred REQUIRED SUCCESS ATTRIBUTE Knowledge Of GxP’s, CGMP And Other Regulatory Requirements. Compliance Collaboration Accountability Customer service orientation Planning and prioritization Secondary Success Attributes Attention to detail People connect Emotional control Effective communication Problem solving Roles

Job Title: Quality Coordinator – Sourcing & NPD Location: Lajpat Nagar, Moradabad, Delhi Industry: Furniture, Home Décor, Manufacturing Job Type: Full-Time | On-site Salary: ₹40,000 to ₹50,000 per month Experience: 5–7 Years (Sourcing, Quality Assurance, Procurement) Education: Bachelor’s degree in Business, Supply Chain, or related field Position Overview We are seeking a dynamic and experienced Quality Coordinator – Sourcing & NPD to manage and elevate our procurement , product development , and quality assurance processes. This role is pivotal in ensuring that all materials, components, and final products meet the highest standards of compliance, consistency, and performance across our furniture and home category . The ideal candidate will be highly detail-oriented, self-motivated, and capable of managing end-to-end sourcing while actively supporting trend-driven new product initiatives and overseeing quality from concept to completion. Key ResponsibilitiesQuality Coordination Ensure all materials, components, and final products meet regulatory and buyer-specific quality standards . Perform regular inspections on production floors including inline, midline, and final inspections based on AQL standards . Assess product samples and components for consistency, craftsmanship, and finish levels before approvals. Identify and promptly resolve any production or quality-related discrepancies , working closely with suppliers and internal teams. Monitor vendor performance and participate in quarterly evaluations to ensure continual improvement. Maintain documentation related to quality checks, vendor audits , and inspection reports for management reference. Collaborate closely with the Product Line, Sales, and Operations teams to ensure timely and successful execution of sampling and bulk orders. Sourcing & Procurement Manage procurement activities across multiple product categories, with a focus on furniture and home décor . Develop and implement a direct factory sourcing strategy to enhance transparency, pricing, and control . Negotiate commercial terms with vendors including pricing, lead times, payment terms , and production capacities. Conduct cost and quality assurance analysis on key items to drive value-based decisions . Work collaboratively with vendors to optimize ranges, improve margin , and mitigate commercial, operational, and contractual risks. Maintain daily updates and communications with local and offshore vendors to ensure smooth operations. New Product Development (NPD) Research and onboard new suppliers using platforms like Alibaba, India Mart, and AliExpress to support NPD initiatives. Coordinate with the HK, Holland, and USA marketing teams to tailor product selections based on trends and seasonal demand. Manage sampling programs end-to-end , including vendor coordination, shipping, and reporting to the Head Office. Create and manage offering and quotation files , including comparison sheets to support sourcing decisions. Maintain accurate databases in Excel for vendor tracking, sample status, pricing , and development stages. Support curated item development based on buyer feedback and market direction. Key Requirements Bachelor’s degree in Business, Supply Chain , or a related field. 5–7 years of experience in sourcing, procurement, buying , and quality assurance within the furniture or home category . Prior experience in buying and vendor negotiations is essential. Experience working with global suppliers is highly desirable. Deep understanding of product materials, manufacturing processes , and inspection standards . Familiarity with global procurement networks and direct factory sourcing . Proven ability to manage cross-functional teams and develop long-term supplier partnerships . Excellent negotiation, problem-solving , and decision-making skills . Highly organized, detail-oriented , and capable of managing multiple concurrent projects . Strong command of Microsoft Excel and documentation practices . Good spoken and written English skills with the ability to handle basic business communication confidently . Relevant Keywords: Furniture sourcing jobs, procurement coordinator, home décor quality control, product development jobs, AQL inspection jobs, Moradabad sourcing jobs, vendor management, NPD coordinator jobs, manufacturing quality assurance, factory sourcing Job Types: Full-time, Permanent Pay: ₹40,000.00 - ₹50,000.00 per month Schedule: Day shift Application Question(s): What is your current and expected CTC? Are you comfortable with the work location of Lajpat Nagar 2 Moradabad, Delhi? How many years of experience do you have in sourcing, procurement, buying, and quality assurance specifically within the furniture or home décor category? Have you worked directly with international sourcing platforms like Alibaba, IndiaMart, or AliExpress for new product development? Are you proficient in maintaining Excel databases for vendor tracking, sampling, pricing, and development stages? Have you conducted AQL-based inspections (inline, midline, and final) on production floors? Work Location: In person

Job Title Manager – MSTG NOSD Business Unit R&D1 Regulatory Affairs Job Classification Code New Function R&D Grade G10 Location Central India (Greenfield Project) Key Responsibilities At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Job Description Responsible for the MSTG-NOSD activity related Technology transfer of new products, site transfer products, commercial launches, LCM activities and CMO activities. Responsible for establishing new procedures, maintaining and updating existing procedures in the MSTG NOSD department. To co-ordinate with Cross Functional Team for execution of Trial, Scale-up, Exhibit, Process validation batches of new Products and commercial launch batches. Responsible for Support in regulatory Audit and Compliance & Query responses for Filed products. Handling & Support of Trouble shooting batches for data comparison and route cause Investigation for commercial products. Responsible for Review, comments and approval of MF, FMEA, RA, BMR & protocol (Sampling plan, Process validation protocol) and other technology transfer documents. Responsible for technical evaluation of new process technology in coordination with procurement team and finalization of User requirement specification. Technical support to plant operations team for upgradation to newer process technologies and better sterility assurance. Technical support for improvement in product robustness. Development of new vendors for process technologies. Responsible for overall development and training of the team members. To ensure compliance to cGMP and documentation for various packing activities. Travel Estimate Low Job Scope Job Requirements Educational Qualification B.Pharm / M.Pharm Experience Tenure : 10-13 Years ( Pharmaceutical Industry experience with Injectable formulation site) Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Job Title Sr. Manager – MSTG NOSD Business Unit R&D1 Regulatory Affairs Job Classification Code New Function Research & Development Grade G9A Location Central India (Greenfield Project) Key Responsibilities At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Job Description Responsible for the MSTG-NOSD activity related Technology transfer of new products, site transfer products, commercial launches, LCM activities and CMO activities. Responsible for establishing new procedures, maintaining and updating existing procedures in the MSTG NOSD department. To co-ordinate with Cross Functional Team for execution of Trial, Scale-up, Exhibit, Process validation batches of new Products and commercial launch batches. Responsible for Support in regulatory Audit and Compliance & Query responses for Filed products. Handling & Support of Trouble shooting batches for data comparison and route cause Investigation for commercial products. Responsible for Review, comments and approval of MF, FMEA, RA, BMR & protocol (Sampling plan, Process validation protocol) and other technology transfer documents. Responsible for technical evaluation of new process technology in coordination with procurement team and finalization of User requirement specification. Technical support to plant operations team for upgradation to newer process technologies and better sterility assurance. Technical support for improvement in product robustness. Development of new vendors for process technologies. Responsible for overall development and training of the team members. To ensure compliance to cGMP and documentation for various packing activities. Travel Estimate Low Job Scope Job Requirements Educational Qualification B.Pharm / M.Pharm Experience Tenure : 14-17 Years ( Pharmaceutical Industry experience with Injectable formulation site) Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Position: Site QA Head Reports to: Site Quality Head Department: Quality Location: Halol Position Summary Manage overall quality assurance oversight and site activities wrt to quality systems: documentation review and SOP update, in-process quality assurance, sampling and batch release, preventive maintenance/calibration/qualification/validation, internal audit, compliance, quality oversight of electronic systems, budget, and continuous improvement of quality systems, RA support, monitoring of pest control, retention sample management as per Good Manufacturing Practices requirements. The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, standard operating procedures, and Sun Pharma policies and procedures. Key Responsibilities Responsible for defining operational strategy and road map for quality assurance management at site. Define site quality assurance goals and strategy in line with Sun Pharma compliance, product quality management objectives and regulatory requirements. Effectively manage the site Quality Assurance activities and resources necessary to smoothly run the QA operation at site. Provide strong leadership and expertise to ensure achievement of all Quality Assurance accountabilities at site. Identify and implement solution for improving existing site quality assurance systems and processes. Coach and develop both direct and, as appropriate, indirect reports through ongoing, example-based performance feedback, annual performance reviews and the provision of training and development opportunities. Ensure that performance issues are managed in a consistent and timely manner. Develop site quality assurance revenue and capital budgets and headcount projections, track and manage expenditures and headcount to budget over the fiscal year. Responsible for ensuring availability of adequate resources, including manpower to maintain compliance with GXP requirements. Assure all time readiness of site for regulatory agency inspections\internal audits and appropriate implementation of corrective actions regarding observations made by the agencies\internal audit teams. Responsible for executing Quality Management Reviews at site, monitor individual Performance and set improvement areas. Responsible for ensuring market complaints, failures, deviations are investigated and corrective and preventive actions are implemented as per set timeline. Responsible for ensuring compliance to regulatory requirements on product, process and release procedures. Ensure release of safe and effective drug products from site as per cGMP requirement and regulatory commitment. Responsible for ensuring smooth collaboration with all Sun Pharma sites and leveraging synergies. Review & tracking of quality assurance metrics e.g. deviation, change control, OOS/OOT, CAPA effectiveness, market complaints with site manufacturing / QC Management and driving them down. Ensure processes for supply chain management / Global Material Sourcing for vendor selection is followed for vendor selection, qualification and monitor vendor quality performance Provide inputs to manufacturing, R&D and PDL work processes to ensure Quality by Design. Accountable for designing/implementing and ensuring compliance to all quality related SOPs, Policies, Standards and QA systems at the site. Facilitate internal and regulatory agency audits, ensuring that findings from site audits are understood, assessed and addressed site wide in a comprehensive manner. Monitor industry trends/issues faced internally and identify scope for improving Site quality assurance management and processes. Responsible for fulfilling all training requirements of quality assurance employees. Ensure the quality policies, standards and procedures for computerized systems are implemented and adhered at site. Ensure all GxP computerized systems are validated in compliance with the quality policies, standards and procedures and are maintained in validated state throughout the lifecycle with adequate security and controls to ensure data security. Review and approve the documents as per quality procedures. Work in partnership with the site cross functions and corporate functions for implementation of new initiatives. Minimum Education/Experience Requirements B.Pharm / M.Pharm 17 to 18 Yrs ( with QA experience in - OSD)

Internal Job Posting Position : Manager-II Department : MSTG Grade : G11 Job Location : Dadra Experience : Below 10 years Job Description To provide support for execution and monitoring of trial, scale up, exhibit process qualification batches. To prepare and review new product documents like material requirement sheet, master formula card, bill of material, master formula, risk assessment reports sampling protocol, reports, exhibit batch manufacturing record and exhibit protocols and reports etc. To prepare and review new product documents like sampling protocol and trial batch reports investigation report/Justification report, additional activity protocol, regulatory evaluation etc. To Provide the regulatory response. To share process knowledge to cross functional departments through presentation for smooth technology transfer To prepare and review investigation report/Justification report, additional activity protocol, regulatory evaluation etc. To review and evaluate product history and process parameters for technical remediation and improvement of product robustness. To prepare and submit the investigation reports for OOS, OOT and any failure for exhibit/validation/commercial batch manufacturing and during stability testing. Track wise related activities Change control/CAPA/Planned deviations/Unplanned deviations related activities etc. To prepare and review product containment approach and risk assessment for new product. To prepare and review risk assessment report for elemental impurities/Nitrosamine impurities/residual solvent. To arrange placebo for quality control testing, change part development and to evaluate feasibility of product etc. To prepare and review statistical evaluation for process evaluation. To prepare and review standard operating procedures, training schedule, and conduct training To participate in various regulatory audits to support the plant.

Job Description Position: QC Section Head – Raw Material Grade: G9B Reports to: QC Head Location: Halol 2 Department: Quality Functional Area: QC Designation: Senior Manager Position Summary Responsible for Raw material section w.r.t. Sampling, Testing and Release of Raw material section in Quality control department. Additionally responsible for review and approval of respective QMS like C hange control, CAPA, Lab Event, OOS, OOT, Incident, Action item in Track wise. The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, Standard Operating Procedures, and Sun Pharma Global Quality Policies, Standards and Procedures. Key Responsibilities Monitoring, Planning and execution activity of all Raw Material, GC, HPLC, RM Sampling. Monitoring of analyzing samples received for Investigation, event, market complaint and Pharmacopoeial evaluation. Document submission for Product Registration, Planning of execution on document preparation and submission for Regulatory filling. Troubleshooting / Training to analyst on regular basis to improve Lab system. Responsible and overview to QC Laboratory Raw Material Department (i.e. GC, HPLC, RM Sampling, etc.). Approve change control, CAPA, Lab Event, OOS, OOT, Incident, Action item in Track wise with respect to QC related activity. Handling of Internal / external audits and compliance activity. Handling of track wise, LMS and Empower software. Timely review, execution and closing of Quality alert and Field alert reports. Timely review, closing and approval of OOS, OOT, laboratory events report in track wise. Follow the EHS policy, standard operating procedures and maintain the compliance to GMP requirements. Handling of Field alert reports and co-ordination in the product recall. Providing early alarms and feedback for Quality Improvements. Education/Experience Requirements M. Sc. In Chemistry 15 years’ experience in QC in pharmaceutical industry. Required Success Attribute Knowledge of GxP’s, cGMP and other regulatory requirements. Primary Attributes Planning and Prioritization Collaboration Accountability Compliance Customer Service orientation Secondary Attributes People Connect Attention to detail Emotional control Effective Communication & Problem solving Working Environment/Physical Requirements Incumbent performs work assignments as per business requirement in Quality control. The incumbent is capable to comply with commitment for the business requirements for QC testing and release. This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

About the Company: We are one of India’s premier integrated political consulting Firms specializing in building data driven 360-degree election campaigns. We help our clients with strategic advice and implementation which brings together data-backed insights and in-depth ground intelligence into a holistic electoral campaign. We are passionate about our democracy and the politics that shape the world around us. We draw on some of the sharpest minds from distinguished institutions and diverse professional backgrounds to help us achieve our goal. The team brings in 7 years of experience in building electoral strategies that spark conversations, effect change, and help shape electoral and legislative ecosystems in our country. Job Summary: We are seeking a detail-oriented and methodical Statistical Analyst/ Statistician to join our analytics team. The ideal candidate will be responsible for collecting, analyzing, and interpreting quantitative data to support strategic decision-making. This role involves developing statistical models, running simulations, and producing reports and visualizations to uncover insights and guide organizational priorities. The role also requires the candidate to be able to report and publish insights from data from time to time. Key Responsibilities: ● Collect, clean, and prepare large datasets from multiple sources for analysis. ● Apply statistical methods and models (e.g., regression, hypothesis testing, inference building, panel, categorical, multilevel models) to analyze trends, patterns and forecast ● Interpret and communicate complex data findings and forecasts to non-technical stakeholders. ● Build and maintain dashboards, forecasts, and ad hoc reports. ● Support survey design and evaluation (sampling, weighting, post-stratification if applicable). ● Collaborate with data engineers, subject matter experts, and decision-makers to define analysis goals. ● Ensure the accuracy, integrity, and privacy of all data processed. Required/Minimum Qualifications: ● Bachelor’s or Master’s degree in Statistics, Mathematics, Data Science, Economics(Econometrics), or a related quantitative field. ● Strong proficiency is a must in Microsoft Excel, Word as well as G-Suites ● Strong proficiency in any statistical software(R/SPSS is preferred) ● Solid understanding of statistical concepts, statistical modelling, including, but not limited to linear and logistic regression, ANOVA, Time-Series Modelling, and Bayesian methods. ● Experience working with large datasets and relational databases(graduate or undergraduate experience will also be considered). ● Excellent analytical, problem-solving, and organizational skills. ● Strong communication skills, especially in interpreting data for non-technical audiences. Preferred Qualications: ● Must have demonstrated ability to manage large data-sets simultaneously with a purpose of building hypotheses and inference testing. ● Proven academic excellence/research experience in quantitative fields such as econometrics, financial , mathematics, bayesian statistics etc. ● Model building experience in Python, R will be an advantage. ● Experience with query writing and data automation related tasks (SQL, VBA etc) is a plus. ● Ability to independently work on multiple projects and/or manage key requirements of internal stakeholders. ● Prior experience/Postgraduate experience in publishing academic research is a plus. Location: BLR - 4th Floor, VK Kalyani Commercial Complex, Opp to BDA Sanky Road, Bangalore,560021

Job Title Senior Manager QC Micro Business Unit Quality Job Classification Code New Function Global Quality & Compliance Grade G9B Location Central India (Greenfield Project) Key Responsibilities At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Position Summary – QC lead's responsibilities encompass ensuring quality standards, leading the QC team, managing processes, and improving quality control measures, including developing and implementing quality control systems and protocols, and training and supervising staff. Responsibilities- Procurement and qualification of environmental monitoring system like viable and non-viable monitoring system Involved during designing parts with respect to the environmental and microbial sampling new process equipment’s and area. To prepare and execution of qualification protocol like URS, DQ, IQ, OQ, PQ and schedule PVPTS protocol. Planning and monitoring of environmental monitoring within facility. Oversight of the aseptic operations, environmental monitoring activity – for viable particle count (VPC) and Non-Viable particle count (NVPC). Evaluation and interpretation of environmental monitoring VPC, NVPC and utility monitoring (nitrogen gas, compressed air, CO2 gas) results. To review trend for viable and non-viable monitoring data and suggest action if any. To review trend of microbiological monitoring of personnel of aseptic area. To participate in the aseptic process risk assessment. To participate in evaluating the sampling locations for environmental monitoring based on risk assessment and critical interventions. Planning and monitoring to maintain all environmental monitoring related all systems To review smoke study protocol and executed videos.Ensure the computerized systems validated in compliance with the quality policies, standards and procedures and are maintained in validated statue throughout the lifecycle. Planning and monitoring for pharmacopeia changes updating CAPEX approval and annual budgeting. To fulfil the regulatory requirements Handling of Environmental monitoring (Viable and non-viable) related incident: To review the incident related to aseptic practices. Participate in the microbiological related incidents, investigation and other microbial impact assessment wherever and whenever required. Planning and monitoring to media fill related activities : Handling of media fill visual inspection activity and media fill video review and summary preparation. To participate in media fill process. Evaluate the protocol for interventions to be performed and review of media fill related documentation. To monitor clean room practices during routine production and media fill runs to evaluate and to suggest improvement in practices if required. Participate in the investigations media fill investigations. Sterility assurance : Responsible for the Aseptic core monitoring and compilation of sterility assurance review board data.Conducting the sterility assurance review board and implementing the actions are derived from sterility assurance review board.Involve implementation of contamination control strategy (CCS) across all the blocks and CCS assessment report review. ACT as system owner and ensure computerized system are validated for its intended use through its lifecycle. Planning and monitoring for training of the analysts and newly joined employee. Planning and monitoring for preparation and reviewing of documents. Timely response to audit compliance. Support the assessment and remediation of identified activities as part of various corporate initiatives. Travel Estimate Low Job Scope Job Requirements Educational Qualification Msc. Microbiologist Experience Tenure : 12 to 15 Years ( Pharmaceutical Industry experience mandatory) Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Job Description Position : QA Head Effective Date Reports to : Quality Head Job Code Department: Quality Grade Functional Area: QA Location: Panoli Position Summary Manage overall quality assurance oversight and site activities wrt to quality systems: documentation review and SOP update, in-process quality assurance, sampling and batch release, preventive maintenance/calibration/qualification/validation, internal audit, compliance, quality oversight of electronic systems, budget, and continuous improvement of quality systems, RA support, monitoring of pest control, retention sample management as per Good Manufacturing Practices requirements. The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, standard operating procedures, and Sun Pharma policies and procedures. Key Responsibilities Responsible for defining operational strategy and road map for quality assurance management at site. Define site quality assurance goals and strategy in line with Sun Pharma compliance, product quality management objectives and regulatory requirements. Effectively manage the site Quality Assurance activities and resources necessary to smoothly run the QA operation at site. Provide strong leadership and expertise to ensure achievement of all Quality Assurance accountabilities at site. Identify and implement solution for improving existing site quality assurance systems and processes. Coach and develop both direct and, as appropriate, indirect reports through ongoing, example-based performance feedback, annual performance reviews and the provision of training and development opportunities. Ensure that performance issues are managed in a consistent and timely manner. Develop site quality assurance revenue and capital budgets and headcount projections, track and manage expenditures and headcount to budget over the fiscal year. Responsible for ensuring availability of adequate resources, including manpower to maintain compliance with GXP requirements. Assure all time readiness of site for regulatory agency inspections\internal audits and appropriate implementation of corrective actions regarding observations made by the agencies\internal audit teams. Responsible for executing Quality Management Reviews at site, monitor individual Performance and set improvement areas. Responsible for ensuring market complaints, failures, deviations are investigated and corrective and preventive actions are implemented as per set timeline. Responsible for ensuring compliance to regulatory requirements on product, process and release procedures. Ensure release of safe and effective drug products from site as per cGMP requirement and regulatory commitment. Responsible for ensuring smooth collaboration with all Sun Pharma sites and leveraging synergies. Review & tracking of quality assurance metrics e.g. deviation, change control, OOS/OOT, CAPA effectiveness, market complaints with site manufacturing / QC Management and driving them down. Ensure processes for supply chain management / Global Material Sourcing for vendor selection is followed for vendor selection, qualification and monitor vendor quality performance Provide inputs to manufacturing, R&D and PDL work processes to ensure Quality by Design. Accountable for designing/implementing and ensuring compliance to all quality related SOPs, Policies, Standards and QA systems at the site. Facilitate internal and regulatory agency audits, ensuring that findings from site audits are understood, assessed and addressed site wide in a comprehensive manner. Monitor industry trends/issues faced internally and identify scope for improving Site quality assurance management and processes. Responsible for fulfilling all training requirements of quality assurance employees. Ensure the quality policies, standards and procedures for computerized systems are implemented and adhered at site. Ensure all GxP computerized systems are validated in compliance with the quality policies, standards and procedures and are maintained in validated state throughout the lifecycle with adequate security and controls to ensure data security. Review and approve the documents as per quality procedures. Work in partnership with the site cross functions and corporate functions for implementation of new initiatives. Minimum Education/Experience Requirements Science or Pharmacy Graduate Equivalent 15 years Required Success Attribute Knowledge of GxP’s, cGMP and other regulatory requirements. Planning and Prioritization Collaboration Accountability Compliance Customer Service orientation Secondary Success Attributes People Connect Attention to detail Emotional control Effective Communication & Problem solving Roles Additional Responsibilities Can Be Assigned As Required. WORKING ENVIRONMENT/PHYSICAL REQUIREMENTS Incumbent performs work assignments in both normal office and non-aseptic manufacturing/packaging environments. Moderate to loud noise level is common in production rooms. The incumbent must be able to comply with the gowning requirements for entry into controlled non-aseptic manufacturing areas, and wear personal protective equipment as required. DELEGATION OF RESPONSIBILITY In the absence of job holder, delegation of responsibility will be as follows: Upward Delegation – Strategic site responsibilities to higher level Downward Delegation – Operational responsibilities to direct reports or similar job role ___________________ __________ Department Head Date ____________________ __________ Human Resources Date This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

Title Senior Manager QC Business Unit QC Job Grade G9B / Senior Manager Location : Ahmednagar Key Responsibilities At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Job Summary To ensure on handling of documents like analytical test procedures, specifications, standard operating procedures from initiation till implementation. To ensure quality control GLP related activities are performed as per SOP for calibration, qualification of instrument and equipment. To ensure sampling activities are performed as per SOP and sample integrity are maintained till analysis completion. To ensure working/reference standards are made available for analysis and timely qualification of standards within due date. To involve in investigations and to collaborate with cross function team for root cause determination and implementation of effective CAPA. To ensure safety and use of required personal protective equipment’s during day-to-day activities. Responsible for carrying out any other responsibilities assigned from time to time orally or in writing by HOD. To maintain and enhance quality index of the site unit data elements pertaining to QC function. Identify the training need and organize for the training to concerned group in QC to avoid event and unconfirmed OOS due to errors during analysis. Essential Job Functions To ensure stability samples are charged and analysis completed within the due date and stability chambers are monitored and maintained at respective conditions. To ensure effective analytical methodology are placed for testing. To ensure analytical method validation and analytical method transfer activities are completed and validated methods are adopted for testing. To ensure sampling activities of RM/Intermediates/Finished as per approved standard operating procedures. To ensure stability study sampling, stability study chamber monitoring and timely withdrawal and completion of analysis. To review the analytical method validation, method transfer, regulatory submission related documents, working reference standard procurements. To co-ordinate self-inspection (internal audit) and its compliances. To approve the lab event/out of specification/our of trend/our of calibration/CAPA/change control/deviation. Ensure trend of quality control errors and effective CAPA implementation. To monitor the compliance with the requirement of GMP. To participate in the management reviews of process performances, product quality and of the quality management systems and advocating continual improvement. To ensure a timely and effective communication and escalation process exists to raise quality issues to appropriate levels of management. To conduct training program and ensure it effectiveness. To ensure quality control GLP related activities are performed as per SOP for calibration, qualification of instrument and equipment. To follow safety & use of required personal protective equipment during day to day activities. To ensure maintenance of housekeeping at shop floor and reporting day to day activities to QC head and in absence delegate change to second line manager. To participate in laboratory internal audits, customer audits, health authority inspection. Awareness of IMS systems (ISO14001:2015 and ISO45001:2018) Travel Estimate Low Job Requirements Educational Qualification M.Sc Chemistry Experience 15+ years Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Job Title: Modern Trade - Sales Manager Location: Patel Nagar, New Delhi Department: Sales – Modern Trade Reports To: Modern Trade Head / Regional Sales Manager / National Sales Manager Job Summary: We are looking for a dynamic and results-driven Modern Trade Manager to drive sales and business development through modern trade channels such as large format retail (LFR), supermarkets, hypermarkets, and organized retail chains. The role will be responsible for growing revenue, building strong relationships with key accounts, and ensuring product visibility and availability. Key Responsibilities: Develop and execute modern trade sales strategies to achieve regional and national targets. Build and maintain strong relationships with key modern trade accounts (e.g., Big Bazaar, Reliance Retail, D-Mart, India Mart Metro, etc.). Negotiate terms of trade, visibility agreements, promotions, and joint marketing plans with key accounts. Ensure proper execution of in-store activities like product displays, planograms, visibility, and stock rotation. Coordinate with supply chain/logistics to ensure timely delivery and inventory management. Monitor market trends, competition activities, and pricing strategy in modern trade outlets. Regularly track and report sales performance, stock levels, and distributor-wise performance. Manage third-party merchandisers and promoters to ensure high retail execution standards. Plan and execute in-store promotions, sampling activities, and seasonal campaigns. Collaborate with marketing and trade marketing teams for new product launches and brand initiatives. Qualifications & Skills: Bachelor’s degree in Business Administration, Marketing, or related field (MBA preferred). 8–12 years of experience in Modern Trade sales, preferably in FMCG or consumer goods. Strong understanding of organized retail and trade dynamics. Excellent communication, negotiation, and interpersonal skills. Proficiency in MS Excel, PowerPoint, and sales reporting tools. Ability to manage multiple key accounts and deliver results under pressure. Willingness to travel for store visits and account management. Preferred Qualifications: Experience working with regional/national chains (e.g., Nature’s Basket, More, Spencer’s, etc.). Knowledge of modern trade software/ERP systems like Busy. Exposure to P&L and budgeting responsibilities. Job Type: Full-time Pay: ₹60,000.00 - ₹80,000.00 per year Work Location: In person

Job Title: BTL & Trade Marketing – Sales & BD Manager (Agency) Location: Vasant Kunj, New Delhi Job Type: Full-time Experience: 3–5 years (can be modified based on requirement) Job Summary: We are seeking a dynamic and result-oriented professional to join our team as a BTL & Trade Marketing – Sales Manager . The ideal candidate will be responsible for planning, executing, and managing BTL campaigns, retail promotions, and trade marketing initiatives for our clients and getting new clients on board. This is a client-facing, field-driven role with strong coordination, vendor management, and reporting responsibilities. Key Responsibilities: BTL Execution: Plan and execute BTL activities like mall activations, in-store promotions, roadshows, RWA activities, Corporate Promotions, sampling campaigns, and product demonstrations. Coordinate with creative and production teams to deliver engaging and timely brand experiences. Managing and introducing new vendors. Managing P&L of the function. Manage on-ground promoters/brand ambassadors and ensure quality control. Trade Marketing: Develop and implement trade promotion strategies at retail points (GT/MT/Channel Partners). Managing and introducing new vendors. Managing P&L of the function. Design and deploy POSM (Point of Sale Materials), merchandising elements, and in-shop branding. Liaise with channel sales teams and distributors for trade schemes and visibility campaigns. Client Servicing & Sales: Act as the bridge between client marketing teams and internal execution teams. Participate in pitches, build presentations, and convert client briefs into activation plans. Maintain and grow client relationships to ensure repeat business and upselling. Making pitches and concepts to get new clients on board. Vendor and Budget Management: Handle vendor empanelment and manage third-party partners for fabrication, logistics, and manpower. Prepare cost estimates, budgets, and ensure campaigns are delivered within timelines and cost. Reporting & Analysis: Monitor campaign performance and provide daily/weekly MIS reports. Analyze campaign results, gather market feedback, and suggest improvements. Key Requirements: Bachelor’s degree in marketing, Business, or related field. 3–7 years of experience in BTL/Trade Marketing in an agency. Strong understanding of retail dynamics and consumer activation. Excellent communication, negotiation, and project management skills. Willingness to travel and be on-ground during campaigns. Preferred Skills: Proficiency in MS Excel, PowerPoint, and project management tools. Exposure to FMCG, Consumer Durables, or Telecom categories. Ability to multitask and manage multiple projects under tight deadlines. Reporting To: Director Salary: As per industry standards + incentives based on performance

MakeMyTrip-GoIbibo data science group is looking for a seasoned data science professional, who can build next-gen travel fintech systems powered via personalized product recommendations/persuasions, real-time pricing and causal algorithms. Responsibilities: Train and deploy best in class deep learning models for ranking, pricing, recommendation, representation learning, FinTech products. Work with stakeholders at various stages of project, lead project development from inception to completion. Be a SQL python ninja, understand data thoroughly, build smart AI/ML systems. Opportunity to work with large click stream e-commerce data sets, at MakeMyTrip and GoIbibo, i. e., in rapidly growing travel space. Build and own robust data science APIs meeting 99% SLA at very high RPS. Also ensure training/inference MLOps rigour. Show business impact while having opportunity to build best in class AI/ML models. Requirements: Bachelor's degree in mathematics, Statistics, related technical field, or equivalent practical experience. A minimum of 8 years of experience (or minimum of 5 years with a Ph. D.) in one or more of the following: ML Modeling, Ranking, Recommendations, or Personalization systems. Knowledge of advanced ML techniques such as Classification, Prediction, Recommender Systems, Dynamic Pricing, Choice modelling, Anomaly Detection Experience with statistical data analysis such as linear models, multivariate analysis, stochastic models, and sampling methods. Experience of deploying models into production is preferred Experience with applying machine learning techniques to big data systems (e. g., Spark) with TB to PB scale datasets. Experience with data querying languages (e. g., SQL), scripting languages (e. g., Python), and/or statistical/mathematical software. Strong research record demonstrated through publications. Experience with design and analysis of experiments. Experience with large-scale A/B testing systems, especially in the domain of online advertising or online commerce.

Roles and Responsibilities Meet S&D targets by effective implementation of area sales & development plans . Develop Sales forecast for all categories based on trends . Develop channel sales strategy for geography assigned in consultation with Manager. Define allocation of sales targets to the different territories in consultation with Manager Sales based on clear understanding of calendar of inputs/market growth/category growth . Plan and achieve distribution expansion as per budget plans . Stocks and logistics planning for the area . Ensure distributor claims are settled in time by proper scrutiny and on field verification . Ensure retention of agreed ROI for the distributors. Implement sales strategy to achieve targets through analysis of Nielson & internal data of various markets. Develop distribution strategy in line with changing channel mix. Track availability of required manpower at DBs as per plan and monitor their performance and highlight deviations of norms to Manager Sales. Execute and track distribution expansion by class of towns, type of OLs and category as per plan and take corrective action, wherever required. Execute distributor MIS packages and ensure requisite compliance from the distributors as per agreed time lines. Build trust and relationship with Modern Trade and Company by providing clarity and solutions to any issue raised by them within a reasonable time frame . Work very closely with Regional Trade Marketing /Key Account teams in management of schemes/promotions/contests being run to promote company brand . Execute specific promotions - exhibitions, sampling, in-store activities etc. in Key A/Cs . Plan for new product launches by channel based on thorough understanding of category and distribution objectives for the products to be launched. Desired Candidate Profile Education Graduate Must, MBA preferable. 3-5 years of experience in General Trade from FMCG industry only. Good understanding of MS Excel is a must. Should be able to read and understand data.