163 Sops Jobs

As an Intern at PLEXO HR Solutions, your day-to-day responsibilities will involve understanding the structure and relationships between various data sources, columns, and variables. You will need to perform in-depth analysis to identify trends, patterns, and anomalies in the data. Additionally, cleaning, transforming, and standardizing data from multiple sources to ensure consistency and accuracy will be a key aspect of your role. Handling missing data, duplicates, and discrepancies efficiently will be crucial to maintaining data integrity. You will be expected to create clear, concise, and visually compelling dashboards to present key findings to stakeholders. Updating and maintaining existing reports and dashboards based on business needs will also be part of your responsibilities. You will have the opportunity to develop and analyze complex "what-if" scenarios to support decision-making processes within the organization. Providing actionable insights and recommendations based on data trends will be essential to driving business outcomes. Supporting day-to-day tasks such as data updates, dashboard maintenance, and performance tracking will also be part of your role. In addition, you will be required to prepare Standard Operating Procedures (SOPs), documentation, and reports to streamline data processes and ensure operational efficiency. About the Company: PLEXO HR Solutions is an HR Consulting firm that specializes in streamlining the hiring process by delivering top-quality, culturally aligned candidates. The company combines data-driven human intervention with intelligent recruitment strategies to ensure the perfect fit for the client.,

The ideal candidate will be responsible for meeting the customer service standards and ensuring that the SOPs related to the department are followed. You will be required to generate data in a timely manner and create store reports. Additionally, you will need to handle DC & DSD GRN, follow up on sales enquiries, and work on improving checkout productivity. You will also be tasked with coordinating with the customer service desk for query resolution and ensuring that store level promotions are communicated effectively. It is crucial to focus on ensuring profitability and effectively managing the team. This is a full-time position based in Thrissur, Kerala, with day shift hours. The candidate should have the ability to reliably commute or plan to relocate before starting work. Preferred qualifications include a Higher Secondary (12th Pass) education and at least 5 years of experience in consumer durables and home appliances. In addition to a competitive salary, the position offers benefits such as health insurance and Provident Fund.,

The Manager Internal Audit at Meril Life Sciences Pvt. Ltd. in Vapi, Gujarat is a crucial role responsible for leading internal audit procedures, ensuring policy compliance, identifying risks, and establishing controls to improve operational efficiency. This position demands a combination of technical expertise, analytical skills, and interpersonal abilities to enhance the organization's governance and processes. Key Responsibilities include: - Overseeing internal audits for a specific business segment, conducting comprehensive audits, and implementing control systems. - Assisting in Enterprise Risk Management initiatives and monitoring high-risk transactions and activities. - Identifying process gaps, suggesting cost-saving strategies, and enforcing corrective controls. - Collaborating with process owners and HODs for audit closure and implementation. Moreover, the role focuses on developing and implementing SOPs and policies, ensuring policy and control adherence through regular audits, verifying assets and inventories, and providing insights and recommendations on Master Management, Contracts, Order Controls, Inventory, and Post-Project Analysis. The ideal candidate should hold a Bachelor's degree or equivalent experience, along with a CA/M.Com/MBA-Finance qualification and possess strong leadership skills to effectively perform the duties of this position.,

As a Senior Executive/ Assistant Manager in the Corporate Quality Assurance Pharmacovigilance department, located in Kandivali - West, Mumbai, your primary responsibility will be to ensure compliance with SOPs of the Corporate Pharmacovigilance cell and Corporate Quality Assurance. You will be expected to assist the Corporate pharmacovigilance cell in overseeing vendor compliance through periodic reviews and vendor audits. In this role, you will act as a liaison with internal and external auditors, taking responsibility for ensuring corrective actions are implemented according to their specifications. Your duties will also include persuading Corporate pharmacovigilance cell staff to adopt and incorporate quality methods into their work processes. As part of your responsibilities, you will be required to conduct internal pharmacovigilance audits, perform CAPA management, and review the change control process, deviations, and related Quality Management System (QMS) documents. Additionally, the role involves travel for conducting audits at corporate offices and various plants. The ideal candidate for this position should hold an M Pharm qualification and possess 4 to 6 years of relevant experience in the field. Effective communication skills, attention to detail, and the ability to work collaboratively with internal and external stakeholders are crucial for success in this role.,

As the Feasibility Lead in Clinical Trials, you will be responsible for managing and delivering comprehensive feasibility assessments for early-phase clinical trials. Your role will involve ensuring the scientific, operational, and regulatory viability of proposed sites and countries, as well as supporting proposal development through collaboration with internal stakeholders and external clients. You will lead feasibility planning and execution to support project bids and early engagement efforts. Additionally, you will drive data-driven site and country selection strategies and serve as the subject matter expert in feasibility best practices to ensure alignment with global regulatory requirements. In terms of subject matter leadership, you will provide strategic input on protocol design, country, and site selection, stay updated on global feasibility trends and regulatory guidelines, and guide teams on interpreting feasibility data in line with business objectives. Moreover, you will contribute to process improvement initiatives and knowledge sharing activities within the organization. Your role will also involve project execution, where you will lead feasibility components across multiple projects to ensure timely and high-quality deliverables. You will be expected to anticipate challenges, design mitigation strategies proactively, and optimize internal resources to manage feasibility timelines effectively. Reporting and documentation will be a key aspect of your responsibilities. You will develop and present regular updates, dashboards, and ad hoc reports for both internal and external stakeholders. It is essential to maintain clear records for audits and client reviews to ensure transparency and compliance. Quality assurance is another crucial area where you will be involved. You must ensure compliance with ICH-GCP, company SOPs, and regulatory frameworks, participate in internal audits, and implement corrective actions as necessary. Promoting a culture of quality and continuous improvement will be integral to your role. Process optimization is also part of your responsibilities. You will contribute to the creation and refinement of SOPs related to feasibility, identify inefficiencies, and recommend enhancements to improve scalability and consistency within the organization. Team development and collaboration are essential components of this role. You will support the onboarding and mentoring of new or junior team members, foster a collaborative work environment, and facilitate cross-functional knowledge sharing. Additionally, participating in resource planning discussions to support strategic growth will be expected. Key Performance Indicators (KPIs) for this role include the timeliness and accuracy of feasibility reports, the success rate of project bids supported, client satisfaction in feasibility discussions, compliance with SOPs and regulatory requirements, contribution to team development and knowledge sharing, as well as clarity and transparency in feasibility reporting. Internal and external collaboration are critical aspects of this role. You will collaborate with department and functional heads internally (e.g., BD, Clinical Operations, Regulatory) and externally with sponsors, clients, and Global Site Networks. Candidate Requirements: - Education: Bachelor's degree in Pharmacy (mandatory); higher degrees in life sciences or clinical research are a plus. - Experience: Minimum 8 years of relevant experience in clinical trial feasibility or clinical development, with exposure to feasibility planning for early-phase clinical trials (Phase I/II) and global clinical trials preferred. - Technical Competencies: Strong understanding of clinical development and regulatory landscapes, proficiency in feasibility platforms, site databases, and data analytics tools, as well as CRM tools and Microsoft Office Suite (Excel, PowerPoint, Outlook). - Behavioural Competencies: Strong decision-making and problem-solving abilities, effective communication and interpersonal skills, coaching and mentoring mindset, ability to collaborate across functions and lead without direct authority.,

You will be responsible for filing monthly returns of Foreign entities and maintaining their bookkeeping. In addition, you will coordinate with international accountants or auditors as necessary. Your role will require a working knowledge of GST, TDS, and Manufacturing company accounts. You will assist in establishing internal controls, SOPs, and audit schedules. Generating and analyzing MIS reports will be part of your responsibilities as requested by management. You will also support the Head of Department in all functions related to accounts. This is a full-time, permanent position. **Education:** - Bachelor's degree (Preferred) **Experience:** - Minimum 3 years of experience in Accounts (Required) - Total work experience of 4 years (Preferred) **License/Certification:** - Visual Catpro certification (Required) **Work Location:** - In person,

As a Manager Training with 5 to 10 years of experience, your responsibilities will be diverse and will encompass various tasks including but not limited to: - Inducting new employees into the company and providing them with an overview of the organization. - Training new employees on the fundamentals of core subject knowledge related to hair and skin care. - Developing and updating Training Manuals for all positions within different divisions. - Assessing and evaluating trainees to ensure their readiness to join the workforce. - Introducing soft skills and refresher training programs, along with creating training calendars and schedules. - Regularly updating the Training Module to keep it in line with the latest industry standards. - Organizing end-to-end training schedules and coordinating grooming and etiquette sessions. - Sharing Standard Operating Procedures (SOPs) and Key Result Areas (KRA) with the trainees. - Providing guidance and support to ensure cost control measures are followed. - Ensuring compliance with Management Information Systems (MIS) and SOPs, and monitoring factors like attendance and punctuality. - Conducting orientation sessions and arranging on-the-job training for new hires. - Evaluating the performance of instructors and the effectiveness of training programs, and making recommendations for enhancements. - Developing and organizing training manuals, multimedia visual aids, and other educational materials. - Maintaining Management Information System (MIS) reports to track training progress. Ideal candidates for this role should have experience in training within the Beauty and Wellness industry, specifically as skin care trainers, hair care trainers, beautician trainers, or skill development trainers. Additionally, candidates with certifications in CIDESCO, Beauty, and Cosmetology are preferred. If you find this profile suitable and meet the required qualifications, please send your resume to hr@richfeel.com.,

As a Plant Tissue Culture Technician specializing in Laminar Room Plant Inoculation, your primary responsibility will involve taking clippings from plants and cultivating them on agar media in sterile containers within a laminar flow hood. This meticulous process, known as micropropagation, necessitates the prevention of contamination from bacteria or fungi, underscoring the importance of proper screening for bacterial and fungal infections in tissue culture bottles. You should possess a minimum of 3+ years of experience working in a plant tissue culture lab, specifically in a laminar room setting for plant inoculation tasks. Your role will entail managing an inventory of chemicals, media, and stock solutions, as well as ensuring the safe disposal of chemical and biological waste. Additionally, you will be responsible for procuring necessary supplies and reagents, maintaining detailed records of orders, and adhering to Standard Operating Procedures (SOPs). Recognizing signs of plant diseases and identifying fungal or bacterial contaminations in the growth room will be crucial aspects of your duties. Moreover, you will be expected to maintain precise records, collect and analyze data, and enter information into spreadsheets. Understanding traceability and logistics, as well as participating in planting, maintaining, and assessing plants for disease resistance and other characteristics, will be integral to your role. Preferred qualifications for this position include experience in horticulture, plant biology, and genetics, along with familiarity with greenhouse and indoor growing operations. Collaboration is key, as plant tissue culture technicians often work as part of a team. A positive attitude and effective communication skills with team members are highly desirable attributes for success in this role. Your salary will be commensurate with industry standards, and immediate availability is required for this position.,

You will be responsible for managing a portfolio of sourcing categories and strategic sourcing projects. Your primary tasks will include developing or refining sourcing strategies for each category, taking ownership of the end-to-end P2P & S2P cycle, and implementing strategic initiatives within an assigned portfolio of clients. It is essential for you to be well-versed in RFI/RFX and E-tendering processes, as well as maintaining a high level of integrity at all times. Your key responsibilities will include being an integral part of the "Procurement Centre of Excellence" and focusing on the following areas: 1. Procurement & Sourcing: - Identifying and evaluating potential suppliers based on cost, quality, reliability, and delivery speed. - Sourcing and procuring raw materials, equipment, and services according to company requirements. - Negotiating contracts, prices, and terms with vendors to achieve cost savings. - Ensuring all purchases align with the budget and company policies. 2. Supplier & Vendor Management: - Building and maintaining strong relationships with suppliers. - Monitoring supplier performance and compliance with contract terms. - Conducting periodic supplier evaluations and implementing corrective actions when necessary. - Resolving any supply issues to prevent disruptions in operations. 3. Purchase Order & Documentation: - Preparing and processing purchase orders with accuracy and completeness. - Maintaining procurement records, including contracts, purchase orders, and invoices. In addition, you must demonstrate expertise across various indirect procurement categories such as Safety, PPE, Fasteners, Hand tools, Motors, Hydraulics, and Office Supplies. Building relationships with suppliers, OEMs, distributors, and dealers to negotiate the best rates and discount structures is crucial to maximize margins on client orders. Compliance with SOPs and internal technology infrastructure, along with continuous improvement to streamline operations, is also expected. Desired Candidate Profile: - 1-2 years of experience in enterprise procurement function in Indirect/MRO categories. - Good working knowledge of purchasing strategies. - Excellent verbal and written communication skills. - Ability to work in a fast-paced environment. - Proficiency in Microsoft Office. If you are a self-starter, passionate about disrupting an industry, and have a high bias for action with a willingness to deliver results, this role might be the perfect fit for you. Your strong client service skills and the ability to inspire and lead a team will be valuable assets in this position.,

The Company Syngene International Ltd. is an integrated research, development, and manufacturing solutions company serving various sectors including pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemicals. With a team of over 4500 scientists, Syngene offers expertise in delivering high-quality science, robust data management, IP security, and efficient manufacturing processes. The company's facilities span over 1.9 million square feet, catering to leading biotech companies and multinational corporations such as GSK and Merck KGaA. Key Responsibilities Safety is a top priority at Syngene, and all employees are expected to prioritize safety in both personal and professional capacities. Compliance with safety guidelines, procedures, and SOPs is mandatory to ensure a safe work environment. Common Responsibilities - Adhere to Environment, Occupational Health, Safety, and Sustainability (EHSS) practices for a safe work environment. - Complete assigned trainings in a timely manner and comply with training procedures. - Participate in mandatory trainings related to data integrity, health, and safety. - Maintain compliance with Good Manufacturing Practices and Good Documentation Practices. - Follow Standard Operating Procedures and Operational Control Procedures. - Support training programs on procedures, protocols, and on-the-job activities. - Report nonconformities and deviations to supervisors or line managers promptly. - Participate in deviations, investigations, CAPA, and change controls as needed. Safety And DI Responsibilities - Follow organizational policies on EHSS, POSH, Data Integrity, and IT security. - Wear applicable Personal Protective Equipment (PPE) and adhere to EHS requirements. - Understand and follow safety protocols to prevent incidents. - Identify near-misses and potential incidents, and report them to supervisors. Specific Responsibilities - Adhere to aseptic behavior in Biologics operations. - Perform upstream activities including Assembly preparation, Media Preparation, Vial thaw, Feed preparation, and Bioreactor Operations. - Monitor and control specific Operations of the upstream processes. - Maintain Quality records and traceability of products. - Perform in-process product sampling and storage. - Review and prepare operation-related documents. - Take responsibility for the assigned USP area and equipment/instrument ownership. - Coordinate with QA for line clearance and maintain process areas for inspections. - Prepare procedures, protocols, risk assessments, and Batch Manufacturing Records (BMRs). - Execute protocols related to upstream activities and equipment/instrument qualification. - Review consumable stock and maintenance records. - Ensure timely closure of work orders and report nonconformities. - Participate in downstream activities under the supervision of downstream supervisors. Syngene International Ltd. is an Equal Opportunity Employer. Visit https://syngeneintl.com/ to learn more about the company and its operations.,

As a Research Associate with a qualification of M.Sc in Industrial or Organic Chemistry and 3 to 6 years of experience, your primary responsibility is to ensure the smooth functioning of various activities related to manufacturing processes. It is essential to join within 2 months for better suitability. Your tasks include: - Acquiring training for each activity and equipment before execution, following the respective Training Needs Identification (TNI). - Adhering to the entry and exit procedures of manufacturing blocks, including chemical and Pharma areas. - Performing all process operations as per the Batch Manufacturing Records (BMR). - Cleaning all equipment according to the Standard Operating Procedures (SOP), Procedure, and Product Cleaning Record (PCR). - Following all current Good Manufacturing Practices (cGMP) requirements in the plant. - Operating all procedures in accordance with safety regulations. - Participating in discussions regarding ongoing and completed operations during shifts and ensuring appropriate charge handover. - Reviewing and verifying the status of equipment and activity logbooks. - Ensuring housekeeping and sanitation standards in the designated areas. - Conducting cGMP and safety talks for department employees. - Verifying raw materials, packing materials, and intermediates issued by the Warehouse. - Segregating raw materials, packing materials, and intermediates in manufacturing storage areas. - Updating equipment/area status board after operational activities. - Performing visual cleanliness verification of operational equipment before starting operations. - Operating various equipment including reactors, filtration equipment, dryers, and powder processing equipment. - Charging and discharging materials as per approved batch manufacturing records. - Sampling in-process and intermediate products and sending samples to Quality Control (QC) for analysis. - Packing and labeling intermediates, drug intermediates, and drug substances. - Operating utility systems as required. - Calibrating/verifying instruments such as pH Meters and weighing balances. - Ensuring completion of preventive maintenance and calibration of equipment and accessories as scheduled. - Ensuring completion of general/breakdown maintenance and permit system requirements. - Proper disposal of solid and liquid wastes along with necessary documentation. - Completing performance qualification/verification of equipment as needed. - Preparation of batch manufacturing records, cleaning records, and Bill of Materials. - Creation of process orders in SAP for raw materials and packing materials. - Preparation of material requisition slips for the issuance of raw materials and packing materials. - Recording activities in respective logbooks as per defined procedures. - Reviewing batch records post-activity completion. - Submitting completed batch records to Quality Assurance (QA) for review and archival. - Complying with QA review observations in batch records. - Verifying equipment and areas before line/area clearance activities. - Generating in-process and other status labels and affixing them as per defined procedures. - Reporting the final output (yield) in SAP. - Performing preventive/general/breakdown and calibration activities in SAP. - Complying with cGMP and safety norms. - Acquiring training on SOPs and batch records and providing training to subordinates as needed. - Participating in internal, customer, and regulatory audits. - Performing any other activities assigned by Head of Department (HOD) post-requisite trainings. - Escalating any issues related to discipline, manpower availability, hygiene, contamination, incidents, or deviations to the appropriate level.,

The Senior Operations Manager position based in Kalyan, Mumbai, India is a full-time role within the Furniture / D2C / Manufacturing industry. As the Senior Operations Manager, you will be responsible for overseeing end-to-end backend operations, encompassing supply chain, production, logistics, warehousing, and post-sales service. This pivotal role directly reports to the founders and plays a crucial part in ensuring the efficient scaling of operations. Your key responsibilities will include managing procurement, vendor relationships, and production processes. Additionally, you will be in charge of coordinating logistics, monitoring inventory levels, and optimizing warehousing operations. Driving quality control initiatives, overseeing dispatch activities, and managing customer support operations will also fall under your purview. You will be tasked with establishing standard operating procedures (SOPs), building and leading operational teams, and developing operational dashboards to enhance efficiency. To excel in this role, you should possess 8-12 years of experience in operations and supply chain management, with a preference for experience in the D2C or furniture industry. Strong skills in vendor management and cost control are essential, along with proficiency in Excel, ERP systems, and other operational tools. An engineering degree is mandatory, while an MBA is considered advantageous. By joining our team, you will have the opportunity to take on a high-impact role in a rapidly growing brand. Working closely with the leadership team, you will be eligible for performance-based incentives, making this a rewarding career opportunity. This is a full-time, permanent position with day shift hours and an in-person work location.,

As an Internal Audit Supervisor in our organization, you will lead a team consisting of Chartered Accountants (CAs) and Civil Engineers. You will be responsible for overseeing the performance of your direct reports, identifying their development needs, and ensuring their continuous on-the-job training. Additionally, you will provide guidance to your team members on work-related matters and assess internal controls while framing and implementing Standard Operating Procedures (SOPs). Your role will involve preparing the Internal Audit Program and Audit Calendar for both the Head Office and various projects. You will establish an audit committee, develop audit strategies, and collaborate with auditees to ensure timely closure of audits. Furthermore, you will be responsible for creating audit reports, discussing findings with departmental heads and Regional Audit Heads, and evaluating compliance with organizational processes and policies to identify financial risks. As part of your responsibilities, you will develop and present comprehensive reports based on audit results, document processes, and review findings with management and other stakeholders. You will recommend process modifications, devise risk mitigation plans to prevent potential fraud or abuse, and propose enhancements to existing controls and processes by revisiting SOPs. In addition, you will conduct ledger scrutiny, analyze trial balances, and reconcile balance sheet accounts to ensure accuracy and integrity of financial data. Your expertise and leadership will play a crucial role in maintaining effective internal audit operations and strengthening the organization's risk management framework.,

You should hold a Bachelor's Degree with a minimum of 17 - 20 years of relevant experience in new loan setup and loan servicing within the Back office/Financial industry. Knowledge of loan systems like Loan IQ/ACBS would be advantageous. Familiarity with Nostro/Cash matching, General Ledger reconciliation, SWIFT, and other remittance systems is required. Strong problem-solving and investigative skills are essential for analyzing and resolving process-related issues. A strong risk & control mindset is necessary, along with experience in driving small to medium-sized projects with successful outcomes. Proficiency in people and performance management, as well as escalation management, is crucial. You will be responsible for closely monitoring the team daily to ensure all SLAs (Quantity & Quality) are met and promptly escalating any exceptions for resolution. Supervising and assessing work allocation, identifying capacity areas throughout the day across all Global sites. Implementing strategies and core objectives in alignment with the global operations roadmap. Ensuring compliance with all controls and JP Morgan requirements, promptly escalating any risk items. Adhering to audit and compliance regulations and serving as the focal point for internal and external audits. Handling complex process-related queries and clarifications from team members as the subject matter expert. You should provide leadership, development, and communicate the vision and objectives for the department to all team members. Collaborating effectively with colleagues across the organization, valuing their skills and experience to achieve shared objectives. Managing individual performance instances and development improvement plans. Identifying process/soft skills-based training to enhance individual performances or growth plans. Developing domain expertise in the team to create subject matter experts. Providing constructive performance feedback monthly and tracking improvement areas. Assisting in the hiring process to backfill attrition or new roles. Motivating staff to meet business priorities and identifying high-potential talent with development plans. Implementing a robust Knowledge Management model including SOPs, process/policy change management, and ongoing training.,

As an Accounts Manager at iTeach Schools, you will have the opportunity to work directly with the Finance Manager and lead a team of 4-5 Associates to oversee the accounting and compliance functions of the organization. Your role will be crucial in maintaining the financial records, ensuring compliance with statutory requirements, managing audits, and presenting reports to the management. Your responsibilities will include monitoring day-to-day accounting activities, preparing financial statements and reports, ensuring compliance with regulations such as FCRA, TDS, PT, IT, PF, ESIC, and GST, managing external and internal audits, and liaising with various stakeholders including leadership, auditors, donors, and program staff. In addition, you will be responsible for creating, reviewing, and updating Standard Operating Procedures (SOPs) across functions, managing expenses in line with approved budgets, refining accounting and reporting systems, and enhancing the capacities of the Finance team. To qualify for this position, you should be a Semi-Qualified CA with at least 3 years of post articleship work experience in accounts, taxation, and financial compliance. Proficiency in Income Tax, TDS, PT, and GST compliance is essential, along with prior management experience. Experience in the NGO sector, as well as knowledge of FCRA, PF, and ESIC, are preferred. The ideal candidate will possess managerial and leadership qualities, be proficient in Excel and Tally, have strong communication and interpersonal skills, and be able to work independently while taking ownership of responsibilities. A logical thinker, effective problem solver, and willingness to learn are key competencies required for this role.,

As a Clinical Research Associate (CRA), you will play a key role in conducting Phase I-IV clinical BA/BE studies. Your primary responsibilities will involve monitoring and managing activities at clinical sites to ensure that project timelines and deliverables are achieved. Building strong relationships with clinical sites and investigators will be essential, along with assessing protocol and regulatory compliance based on local and federal requirements, ICH GCP guidelines, and PSI SOPs. Your focus will be on safeguarding subjects" rights, safety, and well-being, as well as maintaining data quality. Your tasks will include preparing, conducting, and reporting on various activities such as site selection, initiation, routine monitoring, and close-out visits. Monitoring patient enrollment to meet recruitment targets and project timelines will be crucial at both site and country levels. You will be responsible for source data verification, resolving data queries, and conducting ongoing reviews to ensure data quality and compliance with Risk Based Monitoring practices. Timely reporting and follow-up of Adverse Events (AE)/Serious Adverse Events (SAE) and protocol deviations will also be part of your duties. Acting as the main communication channel between the Sponsor and the site, you will serve as a point of contact for in-house support services and vendors. Proper handling, accountability, and reconciliation of Investigational Product(s) and study supplies will be under your supervision. Additionally, you will review essential documents at the site level and ensure the reconciliation of study OSF/TMF at the site and/or country level.,

The job involves being responsible for filing monthly returns of Foreign entities and maintaining their bookkeeping. You will be required to coordinate with international accountants or auditors when necessary. A working knowledge of GST, TDS, and Manufacturing company accounts is essential. Additionally, you will assist with internal controls, SOPs, and audit schedules. Generating and analyzing MIS reports as per management's requirements will also be part of your responsibilities. You will be supporting the HOD in all functions related to accounts. This is a full-time and permanent position. The benefits include commuter assistance and Provident Fund. The work schedule is during the day with a fixed shift. The ability to commute/relocate to Jalandhar, Punjab is necessary. You should have a Bachelor's degree, and a minimum of 3 years of experience in accounting is preferred. Proficiency in English is also preferred. If you are interested in this opportunity, please ensure that you have the required knowledge of GST, TDS, and Manufacturing company accounts. Please note that the work location is in person.,

You will be responsible for assisting in incoming material inspection in accordance with standards and specifications. Additionally, you will provide support in in-process and final product inspection. Your role will involve conducting basic dimensional checks using measuring instruments such as Vernier and micrometer. It will be part of your duties to maintain inspection records and test reports, as well as to support in preparing quality data for audits and internal reports. Furthermore, you will be required to prepare and tag samples for testing or laboratory analysis, ensuring proper sample storage and traceability. Adherence to all quality procedures and standard operating procedures (SOPs) is essential. You will need to ensure compliance with ISO and internal Quality Management Systems (QMS), while also following personal protective equipment (PPE) and safety regulations during inspection activities. This is a Full-time, Permanent job opportunity suitable for Fresher candidates. The work schedule involves Day shift, and the work location is In person.,

As a Supervisor at Sigachi located in Dahej, you will play a crucial role in ensuring the smooth production operations in line with GMP standards. Sigachi, a renowned manufacturer of Excipients for Pharma, Nutra, and food industries, has been a key player in the market since its inception in 1989. With multiple facilities in Telangana and Gujarat, Sigachi has solidified its position as a leading producer of Microcrystalline Cellulose globally. Operating under various certifications like EXCiPACT GMP, SGMP, HACCP, EDQM CEP, and ISO 9001:2015, Sigachi has built a reputation for delivering high-quality products across continents. Your primary responsibilities will include planning and organizing production schedules to meet targets for output, quality, and yield. You will oversee all production operations to ensure compliance with SOPs and GMP standards. Collaborating closely with the Quality Control department, you will focus on continuous improvement and effective resource utilization to maintain quality parameters. Additionally, you will coordinate with cross-functional teams, particularly the Engineering Department, to ensure the production of top-notch quality products. It will be your duty to provide on-the-job training for production staff and maintain updated training records. You will be responsible for reporting deviations, conducting investigations, and implementing corrective and preventive actions as necessary. Moreover, your role will involve coordinating with QA for batch release, investigating non-conforming batches, and ensuring batch identification and traceability. Maintaining equipment/instruments calibration, practicing good housekeeping, and adhering to gowning procedures are also part of your responsibilities. In terms of qualifications, we are looking for candidates preferably with a B.Sc, M.Sc, B.Pharm, M.Pharm, or B.Tech (Chemical) degree. An experience of 8 - 10 years in the Pharma Industry or Excipient Manufacturing sector will be highly advantageous for this role. If you are a self-driven professional with a keen eye for detail and a strong background in production operations, this position at Sigachi offers a challenging yet rewarding opportunity to showcase your expertise and contribute to the company's commitment to excellence.,

As the Station Manager in Hyderabad for CRYOPDP, your primary mission is to ensure seamless operations, superior customer service, and optimal productivity at the Hyderabad branch. You will achieve this through effective leadership, operational excellence, and continuous improvement. Your responsibilities include overseeing day-to-day logistics, managing client relationships, and fostering a collaborative, high-performance team environment while upholding the highest standards of quality, safety, and profitability. Your key contributions will encompass various aspects of branch management, leadership, and development. You will be responsible for managing the entire branch, including overseeing staff, resources, facilities, and day-to-day activities. Additionally, you will control relationships with external agents, vendors, and service providers to uphold quality service standards and contractual obligations. Your role will also involve supporting domestic networks and site coordination for clinical trials and pharmaceutical activities. Client relationship management will be a crucial part of your responsibilities. You will focus on developing and maintaining relationships with existing and new clients, identifying growth opportunities, and expanding the client base. You will also be involved in business development, client follow-ups, and developing new agent networks. Temperature-controlled logistics and cold chain management will be a significant aspect of your role. You will monitor cold chain logistics, ensure quality control, handle temperature-sensitive shipments, and oversee the transportation of time-sensitive goods while complying with cold chain management standards. Operational audits, cost reduction initiatives, emergency shipment handling, and crisis management will also fall under your purview. Team and staff management will be another essential component of your role. You will be responsible for employee management, team supervision, shift and leave approvals, as well as employee recruitment, training, and development. Additionally, you will oversee HR coordination, compliance, and ensure that all operations comply with ISO standards. Financial management tasks will include cost management, petty cash management, quotation support, cost reduction initiatives, project management, pricing, and quotations. Facilities management, office maintenance, administrative support, and data management will also be part of your responsibilities. To excel in this role, you should possess a graduate or post-graduate degree with over 7 years of experience in the temperature-controlled logistics corporate sector. Proficiency in English, Hindi, and Telugu is required, with knowledge of other regional languages considered an advantage. Specific experience in temperature-controlled environments, operational and geographical knowledge, customs and airlines regulations, cold chain management, and supply chain understanding are crucial. Interpersonal skills, proficiency in Microsoft Office, effective communication, analytical skills, and the ability to lead a team are essential for success in this role.,

As a member of the Business Intelligence Team at Howden, a Chart Industries Company, you will be responsible for developing and maintaining business intelligence solutions to drive data-driven decision-making. Howden, acquired by Chart Industries in 2023, is focused on innovation for a greener energy environment. Chart Industries is a global leader in manufacturing highly engineered equipment for the Energy and Industrial gas sectors, with a presence in 40 countries and over 11,000 employees. Your role will contribute to enabling a more sustainable world through the Nexus of Clean Strategy. Your responsibilities will include: - Overseeing End to End Quality Assurance and Control activities for Reciprocating Compressor, from Inward material Quality Assurance to handling Warranty/Customer complaints. - Establishing and maintaining Quality Management System requirements in the Product line. - Creating and maintaining SOPs for QA activities to ensure quality standards are met and aligned with customer requirements. - Developing In-process PPAP for new products and conducting Manufacturing and design reviews for new products and projects. - Liaising with Customers and TPIs for Stage and Product clearance, and training small teams in Quality Practices and Systems. Your work environment will involve: - Coordinating and overseeing Shopfloor activities for 3 to 5 hours a day. - Demonstrating NDT test (Level 2) as needed and using quality engineering methods in inspection. - Collaborating with internal/external stakeholders to meet Product, Process, QMS, and Customer requirements. - Traveling to Customer sites/offices for approximately 30 days a year to understand Quality requirements and support product troubleshooting. Your qualifications should include: - Bachelor's degree in mechanical engineering. - 10 to 13 years of experience in Quality Assurance Activities, with 2 or more years in end-to-end Quality activities. - Preferable experience in Reciprocating compressor products. - NDT Level 2 in RT/UT and MPI/DPT methods preferred. - Six Sigma Green Belt certification is a plus. Chart Industries is an equal opportunity employer, abiding by all applicable local, state, and federal statutes governing non-discrimination in employment. This policy applies to all aspects of employment, ensuring fair treatment and opportunities for all employees.,

As a Quality In-Charge at N2N FIBC Solutions Pvt. Ltd., you will play a crucial role in overseeing all quality control and quality assurance activities within our FIBC production facility located in Nagda, Madhya Pradesh. With over 5 years of experience in the FIBC or Woven Sack industry, you will lead and manage quality control processes across various departments including fabric, printing, stitching, and finishing. Your responsibilities will include ensuring compliance with product specifications and international quality standards such as ISO, FSSC, and HACCP. You will be tasked with developing and implementing SOPs for inspections, coordinating with different teams to address quality deviations, handling customer complaints, conducting training sessions, maintaining quality documentation, and monitoring equipment calibration. To qualify for this role, you should have a Diploma/B.E./B.Tech in Textile, Polymer, or Industrial Engineering (preferred) along with a minimum of 5 years of experience in quality control specifically within the FIBC/woven sack industry. Strong knowledge of fabric testing, UV standards, and migration tests for food-grade bags is essential. Familiarity with ISO 9001, ISO 22000, ISO 14001, and 6:1 SF standards is also required. We are looking for a candidate with leadership qualities, excellent analytical and problem-solving skills, and the ability to work under pressure while focusing on continuous improvement. In return, we offer a competitive salary based on experience, the opportunity to grow within a fast-scaling manufacturing unit, exposure to international quality systems, and a supportive work environment that values innovation and excellence. To apply for this position, please send your updated CV and a cover letter to hr@n2nfibc.com with the subject line: Application for Quality In-Charge [Your Name]. Join us in our commitment to delivering high-quality, safe, and sustainable packaging solutions to clients worldwide.,

As an intern at ThinQ Pharma, your day-to-day responsibilities will involve assisting in formulation and pre-formulation studies, supporting the development of stability and bio batches, helping in maintaining lab records including BMR/BPR and SOPs, coordinating with cross-functional teams such as QA/QC/Production, and performing basic lab tests while ensuring accurate data recording. ThinQ Pharma is an integrated pharmaceutical company with a strong global presence and a reputation for offering world-class products and services. Headquartered in Singapore and operating a fully equipped research center in Mumbai, India, ThinQ Pharma has been a key player in the global market for more than 25 years. With a highly skilled team, the company is committed to providing comprehensive solutions for the pharmaceutical and wellness industries.,

The key responsibilities for this position include coordinating and monitoring production activities across coating, printing, foiling, and frosting units. It is essential to ensure that production schedules are adhered to and deadlines are met while maintaining high-quality standards. Identifying bottlenecks or inefficiencies in processes and assisting in implementing corrective actions are crucial aspects of this role. Collaboration with supervisors and machine operators to manage shift planning and resource allocation is required. Additionally, assisting in documenting and standardizing operating procedures (SOPs) for each process is part of the responsibilities. Monitoring raw material availability and coordinating with the inventory team to prevent production delays is also a key aspect of the role. Supporting quality assurance by ensuring compliance with product specifications and customer requirements is essential. Facilitating communication between departments such as production, quality, maintenance, and logistics is also a part of the job. Tracking and reporting key performance indicators (KPIs) related to productivity, downtime, and process yield is another important responsibility. This position is a full-time, permanent role with benefits including Provident Fund. The work location is in person, and for further inquiries, interested individuals can speak with the employer at +91 9811577431.,

As an experienced and trustworthy Accounts & Finance Head at our direct-to-consumer (D2C) lifestyle brand, your role will be crucial in leading and strengthening our finance function. You will be responsible for preparing accurate financial statements, MIS reports, and dashboards for leadership review. Managing budgeting, forecasting, cash flow planning, and working capital requirements will also be under your purview. Ensuring statutory compliance including GST, TDS, Income Tax, ROC filings, and coordinating annual audits will be essential. You will play a key role in implementing strong internal financial controls and SOPs, monitoring costs, analyzing margins, and driving profitability improvements. Coordinating with banks, financial institutions, auditors, and regulatory bodies will be part of your daily responsibilities. Leading, mentoring, and growing the accounts & finance team will be crucial for the growth of the organization. Additionally, providing financial insights and risk analysis to support strategic decisions will be a key aspect of your role. We are seeking a Chartered Accountant (CA) preferred; however, candidates with an MBA Finance or M.Com with relevant experience may also apply. The ideal candidate should possess 8+ years of experience in accounts and finance, ideally in D2C, retail, or manufacturing. Strong knowledge of Indian accounting standards, GST, TDS, and statutory requirements is a must. Hands-on experience with accounting software such as Tally, Zoho Books, QuickBooks, etc., and advanced Excel skills are required. Excellent analytical skills, attention to detail, and a problem-solving mindset are essential attributes. The ability to build systems and processes for scale, strong leadership, and team management skills are highly valued. A high level of integrity and sense of accountability are key qualities we are looking for in potential candidates. At our brand, we advocate the /SAADAA way of living and believe in simplicity with better basics. If you resonate with the idea of living a fulfilling life through simplicity and find joy in little things, you might be the right fit for our team. We offer a culture of continuous learning, a growth path to becoming a leader, and the freedom to explore, fail, and learn. If you are excited about driving meaning with products, working with a team of empathetic problem solvers, and being compensated right for your efforts, we invite you to be a part of our journey towards a simpler and more fulfilling way of life.,