2653 Labeling Jobs - Page 15

Job Title: QC Technician (Mobile, Laptop & MacBook) cum Office Assistant Location: Bangalore Job Summary: We are looking for a QC Technician cum Office Assistant (fresher or experienced) to support quality checking of mobile phones, laptops, and MacBooks, assist in office work, and travel to other states for device inspection as per company requirement. This is a field + office-based role suitable for candidates willing to learn and grow in the electronics and IT hardware industry. Key Responsibilities: QC Duties (Training will be provided for freshers):Perform quality checks of used mobile phones, laptops, and MacBooks. Check device functionality (hardware/software), cosmetic condition, and accessories. Identify defects and mark grading based on QC checklist. Maintain records and prepare QC reports. Office Assistant Duties: Assist in packaging, labeling, and inventory handling. Support in data entry, Excel updates, and courier coordination. Help maintain cleanliness and organization in the office. Outstation QC Visit: Travel to different states for physical QC inspection of bulk devices. Coordinate with vendors and submit proper QC visit reports to the head office. Travel expenses will be reimbursed as per company policy. Required Skills: Basic knowledge of mobile/laptop hardware preferred (training will be given to freshers). Must know Basic Excel, Basic English, and Hindi. Willingness to travel outside the city/state frequently. Good observation, discipline, and ability to follow instructions. Eligibility: Freshers and Experienced both can apply. Minimum Qualification: 12th Pass / ITI / Diploma / Any Graduate. Must be comfortable with field visits and outstation inspections. Job Type: Full-time | On-site + Field Travel Salary: ₹12,000 – ₹18,000 (depending on experience and skills) Joining: Immediate preferred

Designation: Phlebotomist Role: Field Ops Department: Collection Ops Location: Gurugram About Tata 1mg Tata 1mg is a trusted health partner for end consumers and large institutions. Our Mission is tomakehealthcare understandable, accessible, and affordable for all Indians. Over the past three years, we'veworked to build a healthcare platform that guides customers to the right and affordable care. Today, Tata 1mg is present in 1000+ cities– And we’re just getting started. Leading the chart as one of thetopconsumer health platforms through e Pharmacy, e Diagnostics, e-consult, and offline stores, Tata1mghas delivered over 15M e Pharmacy orders, 2M e Diagnostics orders & 1M+ organic users/day in2022and we are just getting started. Our strongest asset is our 6400+ people enabling us to deliver onourmission consistently. Know more about us: https://www.1mg.com/aboutUs Brief about the Team i. Tata 1mg labs is a state-of-art facility offering the highest quality diagnostic services at the convenience of your doorstep. ii. We pride ourselves on three things; Assured Quality, Best Prices, Excellent Turn Around Time. iii. We believe in providing the highest level of transparency to our customers. iv. Our entire team is dedicated to providing the best customer experience and continuously strives to come up with solutions to remain in line with the needs of our customers. What will you do  Sample collection of customer/patients and rapid testing of samples  Maintaining specimen integrity by using aseptic technique and following standard operating procedures.  Identifying patients and their personal information by reviewing their identity documents  Extracting blood from patients through venipuncture or finger-sticks.  Analyzing blood specimens using the correct testing equipment, when necessary.  Preparing specimens for transportation, including labeling vials accurately and matching blood specimens to patients.  Keeping and maintaining records of patient names, volume of blood drawn, and diagnostic findings.  Cleaning, maintaining, and calibrating laboratory equipment used in the drawing and testing of blood specimens.  Collect and tag specimens exactly as outlined in each medical requisition.  Properly package each specimen What we are looking for  Candidates should have a work experience of 3 year to 10 year in the relevant Phlebotomy domain.  Phlebotomy experience is a mandate, experience in sample collection, knowledge of test, ableto handle patient’s, preparing specimens for transportation including labeling vials accuratelyand matching blood specimens to patients and also have knowledge about Waste management.  Education: DMLT/BMLT  Candidate must have good verbal and written communication skills and knowledge of basic computer.  Candidate must have good knowledge of testing protocols and the use of testing equipment'sand also deliver excellent patient service, answer patient questions, act as a resource for patient information and strengthen the relationship between the patient and our entire medical facility.  Candidate should be ready to travel.

🧾 Job Description: Warehouse Executive Position: Warehouse Executive Location: Pan India (Initial training in Jamalpur, Gurgaon – 7 days) Relocation: Candidate must be ready to relocate anywhere in India Food & Stay: Provided by the company Salary: ₹15,000 to ₹18,000 per month Eligibility: 10th / 12th pass or above Experience: Fresher or experienced both can apply --- Roles & Responsibilities: Receive, store, and dispatch goods in a timely and accurate manner Maintain inventory records and manage stock levels Ensure proper labeling and storage of materials Perform daily warehouse inspections for cleanliness and safety Coordinate with transport and logistics teams for timely dispatch Follow all standard operating procedures (SOPs) of the warehouse Operate basic warehouse equipment if required (training will be provided) Support team members and supervisors in daily warehouse operations --- Key Skills Required: Basic understanding of warehouse and logistics operations Good physical stamina and willingness to work in shifts if required Ability to follow instructions and company policies Basic computer knowledge is a plus Teamwork and time management skills

Supervise daily packing activities to meet production and dispatch schedules. Monitor staff performance, provide guidance, and ensure adherence to quality and safety standards. Allocate work duties to packing staff based on priority and capacity. Ensure that packaging materials are available and properly used. Inspect finished packages for accuracy, labeling, and proper sealing. Maintain cleanliness and order in the packing area. Train new employees on packing procedures and safety protocols. Record production data and generate reports for management. Coordinate with inventory, quality control, and dispatch teams.

•Job profile : * Attend Walk in Customers • Alterations * Display Management * Inventory Management * Labeling & Folding & Packing * Handle Social Media * Should be camera friendly * Participate in Promotional activities such as Youtube and Insta Reels etc. * keeping records * Sales Support etc. * ⁠Good English Speaking * ⁠Must wear western outfits

We are hiring two female staff members for our eCommerce godown. The role involves product packing, labeling, and preparing orders for dispatch. Candidates should be detail-oriented, punctual, and able to work in a fast-paced environment. Basic training will be provided. Location: Saniya Hemad, Surat. Full-time position with a supportive team.

📌 Job Vacancy: Store Keeper Company Name: Vinyork Leather Works Location: Ranipet Website: www.vinyork.com Industry: Premium Leather Furniture Manufacturing Job Type: Full-time Experience: 1-3 years preferred 🧰 Roles and Responsibilities: Maintain accurate records of inventory and stock levels. Receive, inspect, and store incoming materials and supplies. Issue raw materials, tools, and components to the production team as per requirement. Ensure proper labeling, storage, and safety of all goods. Keep the store clean, organized, and well-managed. Coordinate with purchase and production teams for stock planning. Perform regular stock audits and physical inventory checks. Maintain stock register (manual or software-based). Raise alerts for low stock or shortages. Ensure dispatch readiness of finished goods when required. Follow FIFO (First In, First Out) and other inventory best practices. ✅ Requirements: Prior experience in storekeeping/inventory management (preferably in manufacturing). Basic computer knowledge (Excel, Inventory software preferred). Strong attention to detail and organizational skills. Trustworthy and responsible. Able to lift and move goods when required.

We are looking for a dedicated and responsible Packing Boy to manage daily order packing for our e-commerce business. The job involves packing orders for platforms like Meesho, Amazon, and Flipkart, mainly dealing with anime merchandise (figurines, t-shirts, posters, accessories, etc.). 🔧 Key Responsibilities: Pack daily e-commerce orders carefully and efficiently. Ensure proper labeling, taping, and safety of products before dispatch. Maintain cleanliness and organization of the packing area. Coordinate with the dispatch/logistics team for timely pickup. Handle fragile or unique anime merchandise with care.

Job Description : Home Collection Phlebotomist Role: Field Ops Department: Collection Ops Location: Various locations What will you do:  Sample collection of customer/patients and rapid testing of samples  Maintaining specimen integrity by using aseptic technique and following standard operating procedures.  Identifying patients and their personal information by reviewing their identity documents  Extracting blood from patients through venipuncture or finger-sticks.  Analyzing blood specimens using the correct testing equipment, when necessary.  Preparing specimens for transportation, including labeling vials accurately and matching blood specimens to patients.  Keeping and maintaining records of patient names, volume of blood drawn, and diagnostic findings.  Cleaning, maintaining, and calibrating laboratory equipment used in the drawing and testing of blood specimens.  Collect and tag specimens exactly as outlined in each medical requisition.  Properly package each specimen What we are looking for   Candidates should have a work experience of 1 year to 10 year in the relevant Phlebotomy domain.  Phlebotomy experience is a mandate, experience in sample collection, knowledge of test, able to Assist patients, preparing specimens for transportation including labeling vials accurately and matching blood specimens to patients and also have knowledge about Biomedical waste management.  Education: DMLT/BMLT  Candidate must have good verbal and written communication skills and knowledge of basic computer.  Candidate must have good knowledge of testing protocols and the use of testing equipment's and also deliver excellent patient service, answer patient questions, act as a resource for patient information and strengthen the relationship between the patient and our entire medical facility.  Candidate should be Willingness to travel for home collections is required. Education: MLT/DMLT/BMLT Experience: both fresher and experince Requirements: 2-wheeler Mandatory with a valid Driving License CTC: Up to ₹3.6 LPA + ₹3.5/km Duty Timings: 6:00 AM – 3:00 PM rotational shifts

Rhombus Power is purposefully transforming defense and global security enterprises with Guardian, our Artificial Intelligence platform for strategic, operational, and tactical decision-making at the speed of relevance. We provide relevant, actionable, and AI-powered insights at each step in the defense decision-making cycle. Equipped with Guardian's AI-powered tools-- from infrastructure to data to insights -- our clients are able to solve their most complex, interconnected challenges and achieve decision and operational superiority. Come join our cross-disciplinary and world-class team that is delivering game-changing solutions to transform global security. Learn more about Rhombus and watch a demonstration of Guardian, our AI Platform here -- https://youtube.com/watch?v=3PxY6su1Q-Q See the following articles to learn more about what we do: https://foreignpolicy.com/2023/06/19/ai-artificial-intelligence-national-security-foreign-policy-threats-prediction/ https://federalnewsnetwork.com/air-force/2023/12/new-decision-advantage-tool-will-change-how-air-force-makes-investment-decisions/ https://apnews.com/article/us-intelligence-services-ai-models-9471e8c5703306eb29f6c971b6923187 RHOMBUS IS ONLY CONSIDERING CANDIDATES CURRENTLY BASED IN INDIA. NO OTHER LOCATIONS WILL BE CONSIDERED, PLEASE DO NO APPLY IF YOU DO NOT MEET THIS REQUIREMENT. Location India (Remote) Job Description We are a cutting-edge defense technology firm that is renown for building next-generation AI systems for national security applications. We seek highly motivated, execution-focused individuals in India to join our remote team as Data Labeling Specialists for an urgent and high-priority client deliverable involving overhead imagery analysis. As a Data Labeling Specialist , you will play a critical role in training object detection AI by accurately labeling image data. You’ll work within a tightly focused and collaborative team, operating at a high tempo to meet tight deadlines and stringent quality standards. This is an ideal role for individuals who are extremely detail-oriented, analytical, and excited to contribute to impactful defense-related AI work. We will rely on you to produce high-accuracy actions under demanding timelines, over several months. We only seek those that will sustain this work ethic and enthusiasm, and like the rest of us, find ways to exceed expectations. We are considering transitioning select Data Labelling team members into a full-time roles as we scale our work. Responsibilities Accurately Identify, analyze, and label objects in satellite or aerial imagery. Apply sound logic on edge cases and don’t assume when you’re not sure. Communicate! Proactively communicate with project leadership and technical teams to provide updates, transparently reporting on progress, flagging and raising issues about labeling and data workflows. Don’t wait for guidance, test and suggest an improvement! Cultivate expertise and leadership in the imagery analysis domain and gain basic machine learning knowledge to better understand how labels are utilized by our ML algorithms. Qualifications Preference for those that have completed an undergraduate degree; please list your GPA in your CV. Prior experience with imagery analysis, GIS, and labeling is preferred, but not required. Strong command over Microsoft Suite and Google tools such as Excel, Word, Sheets, etc. You must be well versed in file management- we want those who are highly organized! The perfect candidate for this role is someone who is adaptable, highly dependable, and can apply logic to multiple different scenarios concurrently. We’re seeking candidates with proven analytical skills, and are excited to solve complex problems. This position is a remote role, however, candidates must be able to reliably produce, at a high degree of accuracy, over sustained timelines. You must be extremely quality focused, a self-starter with bias for action, and able to work in a fast-paced environment. You must be able to learn quickly and have a baseline of strong computer skills. Benefits Full medical, dental, vision coverage for employee and dependents 401k matching program PTO and Holidays Bonus and other incentive programs Access to mental health program Access to Flexible Spending Accounts for Health Care, Dependent and Commuter About Rhombus Rhombus Power Inc. (Rhombus) is a startup located in the heart of Silicon Valley at Stanford Research Park in Palo Alto. We use cutting-edge cross-disciplinary approaches to solve pressing Big Data and Sensing problems in security, energy, and healthcare. Our advisory board includes two Nobel Laureates and a Draper Prize winner. Rhombus compensates, motivates, and develops employees, who are trusted, empowered, and involved. Employees have clear roles and expectations – and their roles are flexible enough to move at the speed of innovation in order to meet and exceed client expectations. We have a unique culture of global purpose, rooted in the innovation and progress of Silicon Valley. Rhombus knows that diversity is a condition for success. We are committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer.

Job Overview Manage and review expeditable adverse events, product quality complaints and medical information to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. It is the responsibility of the post holder to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost effective manner. The individual will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974, the COSHH regulations 1989 and the EC (European Commission) Directives 1992/3 as documented in the Company’s Health and Safety Manual. Summary Of Responsibilities Assume accountability of quality of the deliverables and implementation of quality processes with minimal support from the Manager. Function as a Point of Contact for the delivery team for regulatory updates, quality concepts, applicable procedures, practices, and conventions on the assigned projects. Act as the process and quality expert for the Client. Work with other team members to analyze Quality findings and help develop action plans. Ownership of responding to and addressing periodic client quality reviews and other ad-hoc client quality findings. Perform ongoing review of a sample of various cases or safety reports for global regulatory submissions, labeling / regulatory documents for Fortrea clients e.g., Annual Reports (IND and other), PSURs, PADERs, Clinical Study Reports, Core Data Sheets, USPI, centralized SPC’s, Med Guides etc. Assist with the overall functional quality operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and review expeditable adverse events, product quality complaints and medical information to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. Provide adequate oversight to ongoing sample case reviews and perform reviews as required. Publish quality metrics based on this review and use it to ensure deliverables meet agreed quality targets. Identify, report quality trends to internal and external stakeholders, suggest corrective actions and monitor the execution and closure. Assume ownership of quality of reports and CAPAs as assigned. Ensure that CAPAs are implemented for the assigned project. Conduct process review in coordination with Project Manager and Quality Manager to identify process gaps and proactively coordinate with the delivery team to develop process standards and suggest process improvements. Measure and track audit readiness for assigned projects. Lead authoring, reviews, training and distribution of SOPs, project specific Work Instructions / convention documents etc. Work with individuals in identifying training needs based on quality review findings. Assist in designing sign-off criteria, development and tracking of training schedule and training material for new hires and existing team. Ensure that periodic feedback is provided to the team based on review findings. Initiate discussion forums on Quality errors within assigned project and identify process improvements, share best practices across projects. Communicate with internal Subject Matter experts to get clarification on case-processing queries and providing feedback to team. Responsible to coordinate and handle queries during the client or external audits of the assigned projects. Assume accountability of supporting the client during regulatory inspections and ensuring quality and timely completion of inspection requests. Responsible for developing Quality Management Plan and / or contributing to the Quality Agreement for assigned projects. Support Computer System Validation related activities as required. To respond/review to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. Review recorded information that may be received over the telephone call, email, fax etc. Execute drug safety data management processes - a combination of call intake review, call dialogue documentation review and case follow-up. Guide safety associates in managing voice calls (as required). Perform any other support activities as assigned – tracking various types of information and metrics, ongoing QC of defined process steps, training, reconciliation of data from multiple sources. Coordinate with the project team to support the Client during regulatory inspections at client sites with support from Quality Manager. Perform Analysis of data and if required, suggest strategies for process improvement/excellence. Perform and Review of analysis of data performed and drive strategies for process improvement/excellence. All other duties as needed or assigned. Qualifications (Minimum Required) Bachelors/Masters/PhD degree in Medicine or Alternative medicine, Medical Science, Pharmaceutical science, Nursing, Life Sciences, or related area. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Experience (Minimum Required) Five years of overall work experience in the pharmaceutical industry, biotechnology, or CRO industry primarily in Pharmacovigilance / Safety writing with at least Two years’ experience in Peer review/Quality review. Knowledge of regulatory requirements viz. GPV and applicable EU and FDA guidelines. In-depth understanding of case processing and assessment. Knowledge of Quality Assurance. Awareness of lean methodology concepts. Technical proficiency with Microsoft Office suite of applications. Preferred Qualifications Include Experience in generating quality metrics with trend analysis, authoring, and coordinating Corrective and Preventive Action Reports is preferred. Experience in assessing quality of a case/safety report from a medical, scientific and documentation perspective is preferred. Physical Demands/Work Environment Office Environment . Available for travel 10% of the time including overnight stays as necessary consistent with project needs and office location. Learn more about our EEO & Accommodations request here.

Job Overview Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary Of Responsibilities Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling, causality, adverse event coding and narrative review. Update and document daily case data, case-feedback in appropriate trackers/tools to facilitate tracking and workflow management. Assume complete responsibility for all assigned deliverables in line with expected quality, compliance, and productivity SLAs and KPIs. Provide training and guidance to the case processing team on medical aspects of case processing, only after a tenure of 1 year. Performs secondary medical review (QC role) and retrospective review of cases reviewed (QA role), as required for measuring quality of deliverables, identifying error trends, training needs and areas of improvement only after a tenure of greater than 1year. Performs aggregate medical review and signal detection/analysis activities, as required. Enhances existing client relationships whenever possible. Creates, maintains, and assumes accountability for a culture of high customer service. Participates in process improvement activities across Company. Qualifications (Minimum Required) Bachelor’s degree in medical science or MD or DO or equivalent degree. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Language Skills: Speaking: English at ILR level 3+ or higher. Writing / Reading: English at ILR level 4+ or higher. Experience (Minimum Required) Working knowledge of medical sciences, diagnosis and therapeutics including drug treatments and procedures. Knowledge and understanding of regulatory requirements for Clinical Research. Knowledge and understanding of ICH-GCP guidelines. Preferred Qualifications Include Good understanding of regulatory requirements relating to Pharmacovigilance. Up to 1 year of pharmaceutical industry experience, including pharmacovigilance (case processing, medical review) and / clinical research. 1 to 2 years of Clinical practice experience. Physical Demands/Work Environment Office or home-based environment, as requested by the line manager. Learn more about our EEO & Accommodations request here.

Job Overview Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary Of Responsibilities Undertake primary medical review of cases, including medical assessment of the case for seriousness, listed/labeling, causality, adverse event coding and narrative review. Update and document daily case data, case-feedback in appropriate trackers/tools to facilitate tracking and workflow management. Assume complete responsibility for all assigned deliverables in line with expected quality, compliance, and productivity SLAs and KPIs. Provide training and guidance to the case processing team on medical aspects of case processing. Performs secondary medical review (QC role) and retrospective review of cases reviewed (QA role), as required for measuring quality of deliverables, identifying error trends, training needs and areas of improvement. Performs aggregate medical review and signal detection/analysis activities, as required. Enhances existing client relationships whenever possible. Creates, maintains, and assumes accountability for a culture of high customer service. Participates in process improvement activities across Company. And all other duties as needed or assigned. Qualifications (Minimum Required) Bachelor’s degree in medical science or MD or DO or equivalent degree. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Language Skills: Speaking: English at ILR level 3+ or higher. Writing / Reading: English at ILR level 4+ or higher. Experience (Minimum Required) Working knowledge of medical sciences, diagnosis and therapeutics including drug treatments and procedures. Knowledge and understanding of regulatory requirements for Clinical Research. Knowledge and understanding of ICH-GCP guidelines. Preferred Qualifications Include Good understanding of regulatory requirements relating to Pharmacovigilance. Up to 2 years pharmaceutical industry experience, including pharmacovigilance (case processing, medical review) and/or clinical research. 1 to 2 years of clinicial practice experience. Physical Demands/Work Environment Office or home-based environment, as requested by the line manager. Learn more about our EEO & Accommodations request here.

Job Overview Manage and review expeditable adverse events, product quality complaints and medical information to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. It is the responsibility of the post holder to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost effective manner. The individual will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974, the COSHH regulations 1989 and the EC (European Commission) Directives 1992/3 as documented in the Company’s Health and Safety Manual. Summary Of Responsibilities Assume accountability of quality of the deliverables and implementation of quality processes with minimal support from the Manager. Function as a Point of Contact for the delivery team for regulatory updates, quality concepts, applicable procedures, practices, and conventions on the assigned projects. Act as the process and quality expert for the Client. Work with other team members to analyze Quality findings and help develop action plans. Ownership of responding to and addressing periodic client quality reviews and other ad-hoc client quality findings. Perform ongoing review of a sample of various cases or safety reports for global regulatory submissions, labeling / regulatory documents for Fortrea clients e.g., Annual Reports (IND and other), PSURs, PADERs, Clinical Study Reports, Core Data Sheets, USPI, centralized SPC’s, Med Guides etc. Assist with the overall functional quality operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and review expeditable adverse events, product quality complaints and medical information to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. Provide adequate oversight to ongoing sample case reviews and perform reviews as required. Publish quality metrics based on this review and use it to ensure deliverables meet agreed quality targets. Identify, report quality trends to internal and external stakeholders, suggest corrective actions and monitor the execution and closure. Assume ownership of quality of reports and CAPAs as assigned. Ensure that CAPAs are implemented for the assigned project. Conduct process review in coordination with Project Manager and Quality Manager to identify process gaps and proactively coordinate with the delivery team to develop process standards and suggest process improvements. Measure and track audit readiness for assigned projects. Lead authoring, reviews, training and distribution of SOPs, project specific Work Instructions / convention documents etc. Work with individuals in identifying training needs based on quality review findings. Assist in designing sign-off criteria, development and tracking of training schedule and training material for new hires and existing team. Ensure that periodic feedback is provided to the team based on review findings. Initiate discussion forums on Quality errors within assigned project and identify process improvements, share best practices across projects. Communicate with internal Subject Matter experts to get clarification on case-processing queries and providing feedback to team. Responsible to coordinate and handle queries during the client or external audits of the assigned projects. Assume accountability of supporting the client during regulatory inspections and ensuring quality and timely completion of inspection requests. Responsible for developing Quality Management Plan and / or contributing to the Quality Agreement for assigned projects. Support Computer System Validation related activities as required. To respond/review to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. Review recorded information that may be received over the telephone call, email, fax etc. Execute drug safety data management processes - a combination of call intake review, call dialogue documentation review and case follow-up. Guide safety associates in managing voice calls (as required). Perform any other support activities as assigned – tracking various types of information and metrics, ongoing QC of defined process steps, training, reconciliation of data from multiple sources. Coordinate with the project team to support the Client during regulatory inspections at client sites with support from Quality Manager. Perform Analysis of data and if required, suggest strategies for process improvement/excellence. Perform and Review of analysis of data performed and drive strategies for process improvement/excellence. All other duties as needed or assigned. Qualifications (Minimum Required) Bachelors/Masters/PhD degree in Medicine or Alternative medicine, Medical Science, Pharmaceutical science, Nursing, Life Sciences, or related area. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Experience (Minimum Required) Five years of overall work experience in the pharmaceutical industry, biotechnology, or CRO industry primarily in Pharmacovigilance / Safety writing with at least Two years’ experience in Peer review/Quality review. Knowledge of regulatory requirements viz. GPV and applicable EU and FDA guidelines. In-depth understanding of case processing and assessment. Knowledge of Quality Assurance. Awareness of lean methodology concepts. Technical proficiency with Microsoft Office suite of applications. Preferred Qualifications Include Experience in generating quality metrics with trend analysis, authoring, and coordinating Corrective and Preventive Action Reports is preferred. Experience in assessing quality of a case/safety report from a medical, scientific and documentation perspective is preferred. Physical Demands/Work Environment Office Environment . Available for travel 10% of the time including overnight stays as necessary consistent with project needs and office location. Learn more about our EEO & Accommodations request here.

Dameasy Consumer Products is redefining everyday food through innovation, quality, and smart packaging. Our fast-growing facility in Gurugram spans pilot- to commercial-scale production and supports multiple product lines across sauces, beverages, and convenience foods. What You’ll Do 1. Drive Product Development • Create and refine scalable recipes for sauces, drinks, and packaged foods. • Convert product briefs into cost-efficient, shelf-stable formulations. 2. Run R&D Lab Operations • Oversee daily trials, equipment, and hygiene in the lab-kitchen setup. • Keep clear batch records, SOPs, and sample testing logs. 3. Collaborate with Manufacturing • Partner with production teams to ensure smooth scale-ups and process controls. • Attend line trials and troubleshoot processing parameters on the floor. 4. Source & Evaluate Ingredients • Assess raw materials and additives for functionality, compliance, and cost. • Work with suppliers on samples, technical data, and innovation pipelines. 5. Ensure Regulatory Compliance • Maintain formulation sheets, nutritional data, and shelf-life documentation. • Verify adherence to FSSAI standards, labeling norms, and internal QA specs. 6. Work Cross-Functionally • Provide technical inputs to marketing and packaging for launches and claims. • Support sensory evaluations and cost optimisation with procurement teams. What We’re Looking For • B.Tech or M.Tech in Food Technology, Food Science, Dairy Technology, or related field. • 2-5 years of hands-on experience in food NPD or manufacturing environments. • Solid grasp of ingredient functionality, processing techniques, and compliance. • Comfortable working in R&D labs and factory settings, with strong documentation skills. What You’ll Gain • Ownership of projects from concept to market launch in multiple categories. • Exposure to both bench-top innovation and full-scale manufacturing. • A collaborative, learning-driven culture in a rapidly expanding food brand.

About Us: Platton Inc. is an international, asset-based supply chain services and solutions company. Our services include air and ocean freight forwarding, customs brokerage, contract logistics, warehousing and distribution, truckload and LTL brokerage, and digital logistics solutions for importers and exporters. We serve clients across various industries with a strong focus on automation, visibility, and client success. Position Overview: The Final Mile Logistics Coordinator will be responsible for managing the final leg of domestic freight movement in the U.S., with a focus on LCL deliveries, airport cargo, and Amazon FBA shipments. This role involves close coordination with vendors, delivery partners, and internal teams to ensure on-time delivery, system accuracy, and full compliance with client and regulatory requirements. You will be expected to proactively manage carrier communication, resolve delivery issues, and ensure all milestones are updated in the system to support end-to-end visibility. Core Objective: To ensure efficient, compliant, and timely last-mile delivery of U.S. inbound shipments by managing domestic vendor coordination, execution accuracy, and system tracking. Key Responsibilities: Coordinate LCL final mile deliveries from U.S. CFS locations to residential and commercial consignees Manage air cargo delivery, including coordination with airline warehouses and terminals Handle Amazon FBA deliveries, ensuring booking windows, labeling, and appointments are compliant Source, onboard, and communicate with U.S.-based trucking vendors for last-mile services Update internal systems with delivery statuses, PODs, and tracking details within 24 hours Serve as the first point of contact for delivery issues, delays, redeliveries, or vendor disputes Ensure compliance with Amazon routing guides, TSA regulations, and internal SOPs Provide regular updates to the operations team, including late delivery alerts and vendor performance reports. Required Skills & Experience: 2+ years of experience in freight forwarding or last-mile logistics (LCL, air freight, or Amazon FBA focus) Strong understanding of last-mile delivery operations and accessorial management Experience working with Amazon FBA procedures and U.S. airport cargo operations Proven ability to manage multi-vendor communication and resolve issues in real time Strong command of English (written and spoken) Familiarity with logistics systems or TMS platforms for tracking and documentation Highly organized, self-motivated, and able to work independently in a remote environment Existing contacts with U.S. local delivery and airport cargo vendors Experience with Amazon Seller Central or other delivery portals Understanding of TSA rules, POD standards, and CFS procedures Working knowledge of Incoterms and freight charge validations

Job Title: Project / Sourcing Executive – Operations Eligibility: B.Tech (IIT / NIT only), 0 to 2 Years Experience Verticals: AI Data Collection / Recruitment Sourcing Location: Gurgaon (Hybrid – 5 Days WFO, 1 Day WFH) We are hiring B.Tech graduates from IITs/NITs (0–2 years of experience) for the role of Project / Sourcing Executive – Operations . This role offers a high-growth opportunity for individuals who are proactive, detail-oriented, and eager to take ownership in fast-paced, execution-focused environments. You Will Work Across Either Of The Following Verticals AI Data Collection Recruitment Sourcing This is an operations-heavy role that requires high ownership, adaptability, and the ability to collaborate with remote teams across multiple domains. Key Responsibilities - Sourcing Executive Be responsible for sourcing candidates through various platforms. Expand the business by achieving specific target KPIs. Engage in team management activities. Manage the integration of CRM and ATS for both internal and external stakeholders. Oversee daily operations management along with the team. Focus on data analysis and developing effective strategies for revenue growth. Key Responsibilities - Project Executive Manage end-to-end execution of AI data collection projects (speech, video, text, image, etc.) Coordinate contributor onboarding, training, and daily productivity Work closely with the QA team to ensure compliance with data quality and project-specific guidelines Monitor real-time dashboards, progress trackers, and ensure timely deliverables Collaborate with internal tools teams, freelancers, vendors, and clients across multiple time zones Prepare project updates, reports, and flag risks or delays proactively Identify sourcing needs and coordinate with recruitment/crowd teams for the contributor pipeline Maintain adherence to international privacy, compliance, and client-specific data standards Preferred Qualifications B.Tech from Good Pedigree - IIT / NIT Good communication and stakeholder management skills Detail-oriented, process-driven, and hands-on with documentation and reporting Comfortable working in fast-paced, dynamic environments with tight deadlines Good to Have Prior exposure to data labeling, transcription, speech, or video-based AI projects Experience working with international vendors or contributors Multilingual capability is a plus Skills: documentation,reporting,project management,stakeholder management,sourcing candidates,ats management,data collection,project,data analysis,crm integration,team management,data,iit,sourcing,recruitment,nit,operations

Position: & Simulation Tirage Engineer Work Location: Work from Office / Remote Type: Full-time Shift: Flexible to work in shifts, including night shifts on client request Communication Skills Requirement: Minimum CEFR B2 level of English Technical Skills Requirement: LiDAR L3 About the Role (Position Summary) This role requires a strong combination of technical expertise in AV sensor data (especially LiDAR and camera), meticulous attention to annotation quality, and hands-on experience in simulation data triage. The ideal candidate will work on identifying errors, inconsistencies, and gaps in annotated datasets and simulation scenes, supporting the retraining and validation cycles of autonomous vehicle (AV) systems. Education Qualifications Bachelor's degree in Engineering, Computer Applications, Data Science, or related technical discipline. Experience 3–7 years of experience in annotation, simulation validation, or auditing roles with increasing leadership responsibility. Strong background in LiDAR and sensor data (2D/3D bounding boxes, polygons, cuboids, segmentation). Experience in simulation scenario review and tirage pipelines (e.g., triaging data for model retraining). Prior exposure to client interaction and cross-functional coordination (e.g., with engineering and QA teams). Hands-on experience working in tool-based labeling pipelines and simulation-driven testing environments. Experience working with annotation tools and QA checklists based on project-specific SOPs. Capacity of data analysis towards identifying consistent gaps Desired Qualifications and Experience (if any) Auditor-Specific Soft Skills Exceptional attention to detail: Ability to notice minute annotation errors, shape irregularities, and alignment mismatches. Strong visual-spatial reasoning: Capability to interpret 3D point clouds and assess object depth, perspective, occlusion, and context. Critical thinking: Skill in evaluating edge cases and understanding when annotations fail to represent real-world driving scenarios accurately. Strong ability of pattern recognition Annotation guideline interpretation: Ability to deeply understand, question, and apply detailed project-specific SOPs and edge-case rules. Bias awareness: Understand and flag biases in annotation or scene interpretation (e.g., object labeling errors due to weather, occlusion, or human assumptions). Clear written communication: Document audit findings, feedback, and edge cases in structured and unambiguous formats. Consistency under repetition: Maintain high focus and precision while reviewing large datasets with repetitive structures. Curiosity and domain awareness: Stay engaged with AV trends, annotation standards (e.g., KITTI, nuScenes), and common model failure patterns. Collaboration mindset: Willingness to work closely with fellow auditors, QA teams, and simulation engineers to improve annotation and tirage workflows. Technical Skill Requirements Annotation Auditing & Data QA Annotate and/or Audit 2D/3D sensor data annotations to ensure they meet the project’s accuracy, completeness, and consistency requirements. Identify common error types and provide actionable feedback. Simulation Tirage Evaluate simulation data for complexity, relevance, and anomalies. Tag and classify scenes based on criticality for model training or validation pipelines. Clear understanding of road sign and rules from a driver's perspective with capacity of (given) situation analysis Rules of the Road Expertise: Familiarity with standard traffic behavior, signage, signaling, right-of-way principles, and vehicle interactions under typical U.S. driving conditions. MUTCD Knowledge: Working knowledge of the Manual on Uniform Traffic Control Devices (MUTCD), especially as it applies to lane markings, signage, and signal interpretation across varied roadway types. Passenger Comfort Sensitivity: Ability to assess scenarios from the perspective of a rider, identifying discomfort or unsafe behaviors that may not violate technical rules but still degrade the end-user experience. Driver Duty of Care Perspective: Ability to evaluate edge cases and ambiguous situations through the lens of a responsible human driver, balancing legality with caution and accountability in mixed-traffic environments. Tool & Workflow Expertise Operate advanced tools such as Labelbox, Scale AI, Supervisely, CVAT, CARLA, or in-house labeling systems. Suggest refinements in annotation and tirage flows to reduce ambiguity and improve cycle efficiency. Documentation & Reporting Maintain issue logs and generate structured audit reports. Provide detailed scene-level comments to support iterative data improvements. Responsibilities (not limited to) Conduct systematic reviews of AV sensor annotations using defined QA guidelines. Perform simulation scene triage to identify edge-case scenarios and misclassified outcomes. Tag errors, provide audit-level feedback, and ensure data is looped back for correction or retraining. Collaborate with QA reviewers, annotation operators, and simulation engineers. Contribute to refinement of SOPs and visual reference materials based on audit insights. Stay current with industry annotation standards and simulation evaluation protocols.

About The Role: We are looking for a Dispatch Executive to help us manage and send out our products for corporate incentive programs. You’ll make sure orders are packed correctly, all documents are ready, and products reach our clients on time. It’s a job that needs someone careful, organized, and good with Excel. Key Responsibilities:-  Plan & coordinate daily dispatch schedules for timely deliveries  Prepare dispatch documents: invoices, delivery challans, E-way bills, gate passes  Verify goods before dispatch for quantity, packaging & labeling accuracy  Coordinate with warehouse staff, transporters, and drivers for vehicle placement & loading  Track vehicle movement to ensure on-time delivery to customers / sites  Maintain dispatch records and update ERP / Excel for inward & outward stock  Follow up on PODs (proof of delivery) and resolve delivery issues  Ensure compliance with transport norms and internal documentation policies . Desired Candidate Profile: Graduate or Diploma in any discipline  1–4 years of hands-on experience in dispatch/logistics operations  Familiar with documentation (E-way bills, LR, POD, invoices)  Strong coordination & communication skills  Proficient in basic Excel (VLOOKUP, HLOOKUP, Pivot Tables preferred)  Exposure to ERP / WMS systems is an added advantage  Female candidates preferred (as per current team balance) Key Skills:  Dispatch Planning & Scheduling  Transport & Vendor Coordination  Inventory Outward / Gate Pass Handling  E-way Bill & Delivery Documentation  POD & Delivery Follow-ups  Advanced Excel & ERP updates . Contact us - 7876212244 Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Food provided Life insurance Paid sick time Paid time off Schedule: Day shift Morning shift Supplemental Pay: Performance bonus Yearly bonus Experience: Dispatching: 1 year (Required) Location: Chandigarh, Chandigarh (Required) Work Location: In person

Position Overview: A Pharmacy Assistant supports pharmacists in the day-to-day operations of a pharmacy. This includes assisting with the preparation of medications, managing inventory, ensuring proper patient care, and performing administrative tasks. Pharmacy Assistants play a key role in providing excellent customer service and maintaining a clean, organized pharmacy environment. Key Responsibilities: Medication Preparation and Dispensing: Assist pharmacists in preparing prescriptions, including counting, labeling, and packaging medications. Verify patient information to ensure accuracy of prescribed medication. Prepare medication orders for patients under the supervision of a pharmacist. Customer Service: Greet customers, answer basic inquiries about medications, and provide general assistance. Respond to customer questions about over-the-counter products. Assist with handling phone orders and follow-up inquiries. Inventory Management: Stock shelves with medications and supplies, ensuring products are correctly labeled and within expiration dates. Monitor inventory levels and reorder products as necessary. Assist with organizing the storage of pharmaceuticals. Administrative Support: Process prescription orders and maintain records in the pharmacy system. Maintain and update patient records. Perform clerical duties such as filing, faxing, and other paperwork as needed. Compliance and Safety: Ensure the pharmacy complies with local regulations and standards regarding controlled substances, labeling, and dispensing practices. Assist with maintaining a clean, safe, and organized pharmacy environment. Assist in Health Promotions: Provide educational materials about health products and wellness programs. Promote the pharmacy’s services and seasonal promotions. Skills and Qualifications: High school diploma or equivalent (required). Certification as a Pharmacy Assistant or Pharmacy Technician (preferred but not mandatory). Previous experience in a pharmacy or healthcare setting is an advantage. Knowledge of pharmaceutical terminology, medication names, and their uses. Strong attention to detail and ability to manage multiple tasks. Good communication skills, both written and verbal. Ability to work well in a team and independently. Proficiency in pharmacy management software and basic computer applications. Job Type: Full-time Pay: From ₹14,000.00 per month Experience: total work: 1 year (Required) Work Location: In person Expected Start Date: 01/08/2025

IZARA SPECIALITY EYE HOSPITAL is a Super-Speciality Eye care facility in Central Kerala, being operational in Kayamkulam, Pathanamthitta, Kottayam& Thiruvananthapuram. Pharmacist is responsible for preparing, dispensing, and ensuring the safe and effective use of medications for hospitalized patients. They collaborate closely with healthcare professionals to ensure optimal patient outcomes and adhere to all legal, ethical, and institutional standards. Key Responsibilities: Dispense prescribed medications accurately and safely. Review prescriptions for errors, interactions, and contraindications. Ensure proper storage and labeling of drugs. Provide drug information and guidance to healthcare providers and patients. Participate in patient care rounds and clinical discussions. Monitor patients for adverse drug reactions and efficacy. Maintain stock levels and order medications as needed. Ensure all medicines are stored according to safety guidelines. Check for expired drugs and dispose of them properly. Maintain accurate records of medication use and patient interactions. Ensure compliance with hospital policies and government regulations. Participate in audits and quality assurance programs. Educate nursing and medical staff on new medications and protocols. Stay updated on pharmaceutical developments and continuing education. Required Qualifications: Bachelor’s or Doctor of Pharmacy (B.Pharm or Pharm.D) Valid pharmacist license/registration Clinical pharmacy training or hospital pharmacy experience preferred Excellent communication and interpersonal skills Attention to detail and high level of accuracy Problem-solving and decision-making abilities Ability to work under pressure and in a team environment Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Cell phone reimbursement Health insurance Paid sick time Provident Fund Schedule: Day shift Morning shift Supplemental Pay: Performance bonus Yearly bonus Language: Hindi (Preferred) Work Location: In person Expected Start Date: 05/08/2025

Your responsibilities as Logistics Coordinator Confer with warehouse workers to decipher when delivery truck/vehicle arrive and make plan to receive them. Responsible for counting and supervising of inventory loaded into /unloaded from truck. Performing daily inspection of the warehouse grounds. Responsible for crosschecking the items at the time of loading and unloading of materials. Supervising all warehouse workers and daily activities done by each worker. Maintain FIFO on all stock. Ensuring the loaded items correspond to the pick list generated. Maintain storage area by organizing floor space; adhering to safety and storage layout specifications. Managing the stock in the warehouse in an orderly manner along with systematic labeling and identifiers Responsible for maintaining the bin card updating system in proper manner. Responsible for maintaining inventory by conducting daily RST (Random Stock Take) and weekly full stock count. Responsible to assign duties to workers based on their experience. Supervise and control order picking, goods in, goods out; operations to ensure accuracy with minimum handling and stock damage. Assist the warehouse workers to lift and carry items to awaiting delivery trucks, ensuring that the workers have properly and safely loaded the items onto the vehicles and secure the same. Confirm proper and timely delivery of products. Motivate and encourage teamwork within the workforce for attaining the warehouse objectives. Ensure the general cleanliness and maintenance of the warehouse space and equipment’s. The required skills for this role are: - Good communication Ability to manage warehouse. Interpersonal skills Ability to handle contingencies Time management skills Reporting skills Team player Leadership skills Languages needed: - Malayalam English (Optional) Job Type: Full-time Pay: ₹16,000.00 - ₹18,000.00 per month Benefits: Health insurance Schedule: Day shift Education: Diploma (Preferred) Location: Thiruvananthapuram, Kerala (Required) Work Location: In person

· Education Qualification : B.E/B.Tech/Diploma-Civil · Relevant Experience : 4 -10 · Location : Jagital Hyderabad · Industry preferred : Engineering & Construction · Number of Positions open : 5 Ø Study the Drawings, Quantity & material take off. Ø Check shuttering and bar bending work as per requirement Ø Planning and indenting daily requirement of Labor, construction machinery, materials and formwork. Ø To maintain day to day record DPR & WPR and Submission of daily, weekly, and monthly reports. Ø Monitoring Concrete Work and Preparation of checklist for concrete. Ø Day to Day management of site & Supervision of Masonry, Structures & Finishing works, and Obtaining measurements from site execution engineers. Ø Ensuring that the planned output is achieved from manpower, machinery and Materials. Ø Ensuring proper housekeeping during execution for better material shifting and hassle-free work. Ø High perfection in Marking and execution of civil works such as footings, columns, slabs, block work, and to execute all finishing works such as plastering, marble work, tiles work, false ceiling work, painting work (internal and external also), Aluminum work (windows &door) stainless steel work staircase & balcony area and Ac Work. Ø Support and execute the works as per the schedule and plan the activities with look ahead attitude. Ø Ensuring that all materials used, and work performed are as per specifications. Ø Planning of Materials and proper planning to avoid wastages in the site. Performs other duties and responsibilities as may be assigned from time to time. Ø Coordination with other trades (MEP, Landscape etc.) while executing the works. Ø Manage and develop Cordial relation with all vendors for completion of their scope of work. Ø Conduct periodic reviews with HODs and set out process for speedy redresser of execution bottlenecks. Escalate to line & functional HODs wherever needed to ensure quality & timeliness. Ø Responsible for 100% compliance in statutory and regulatory matters. ➢ Good knowledge and exposure of civil work like RCC Structure, Steel, reinforce meant, plaster work, layout labeling, shuttering work as per drawing etc. ➢ Controlling the time, cost, and quality of construction projects. ➢ Demobilize projects, resources, equipment on completion. ➢ Ensuring smooth Project closure activities- surplus material/resources reconciliation, Sign-offs, commissioning certificate, contractor retention #Immediatejoiners / who can join within hashtag#30days. Interested candidates can drop your resume #recruitment@vensainfra.com with the subject line #Designation Please mention in the email: - What is your overall experience? - Current CTC - Expected CTC - NP Job Type: Full-time Pay: ₹15,000.00 - ₹35,048.34 per month Benefits: Food provided Health insurance Provident Fund Work Location: In person

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . Upload health authority correspondence into BMS's RIM system including the required metadata. Create Health Authority queries in RIM and track to closure. Ensures the correct keywords and submission/ correspondence linkages are established in RIM. Create Commitment records in RIM and send workflows/reminders to users on a regular basis. Responsible for contacting users when data quality findings are identified and ensures issues are corrected. Create and distribute global CMC Change Controls and IMP Amendment events for commercial and investigational products. Issue workflows in RIM to request assessments and submission planning. Send reminders, as needed, and track the events to closure. Create and distribute global Labeling Change Control events. Issue workflows to request assessments and submission planning. Send reminders, as needed, and track the events to closure. Perform data quality checks on Labeling Events which drive reporting to the BMS Labeling Office. Send routine reminders to local markets to correct labeling data quality findings identified through RIM reports. Summarize and track issues. Create Investigator Brochure events in RIM and close out events as requested. Create Marketing and Investigational registrations and update as needed, based on information gathered through RIM reports. Work autonomously with local markets to troubleshoot and resolve issues. Provide user support and address questions as needed. Prompt attention to business-critical activities to ensure compliance and appropriate documentation of regulatory approvals. Key Competency Requirements: Proficient knowledge of global regulatory practices and regulatory operations Knowledge of regulatory information management and submission guidelines and requirements Knowledge of various types of health authority interactions, including HA correspondence, HA queries and HA commitments Experience and knowledge in regulatory information management software and computer systems (Microsoft Office, Outlook, eCTD viewers and web based applications) and technically skilled with such systems. Communicates questions and issues as they arise with possible solution Supports other functions as appropriate Effective written and verbal communication skills Works with supervision Ability to prioritize and strong attention to detail Experience instructing/ training end-users Experience in the development of work instructions and quick reference guides Communication and change management skills Educational Qualifications: BA/BS degree, science / technology field preferred. Experience Requirements: 4+ years pharmaceutical experience; 1+ year of regulatory operations experience . If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Location: Gunded village, Balanagar Mandal, Mahabubnagar dist Department: Production Employment Type: Full-Time Experience Required: 0–2 Years Reporting To: Production Supervisor / Shift In-Charge About the Role: We are looking for a dedicated and energetic Junior Plastic Moulding Machine Operator to join our production team. The ideal candidate will assist in operating plastic injection moulding machines, perform basic quality checks, and maintain cleanliness and safety on the shop floor. This is an excellent opportunity to gain hands-on experience and grow in a structured manufacturing environment. Key Responsibilities: Assist in operating and monitoring plastic injection moulding machines. Load raw materials (plastic granules, additives) into the machine hopper. Remove finished parts from the mould and perform basic visual inspections. Trim, clean, or finish plastic components as per work instructions. Follow machine operator instructions on settings and part removal process. Ensure proper stacking and labeling of moulded parts for further processing. Maintain cleanliness around the machine and workstation. Report any machine irregularities or product defects to the supervisor immediately. Adhere to all shop floor safety rules and wear required PPE. Support senior operators and technicians during mould changeovers or machine maintenance. Required Skills & Qualifications: 10th Pass / ITI / Diploma preferred (Mechanical, Plastics, or relevant field). Basic understanding of machinery operation and factory work practices. Willingness to work in shifts (rotational/day/night). Physically fit to stand for long hours and lift parts as required. Ability to follow instructions, learn quickly, and work in a team environment. Hindi is mandatory along with local language Desirable (But Not Mandatory): Prior experience in plastic moulding or similar factory environment. Exposure to injection moulding, blow moulding, or extrusion machines. Perks & Benefits: On-the-job training by experienced operators. Opportunities for promotion to senior operator level. Job Type: Full-time Pay: ₹20,000.00 - ₹22,000.00 per month Schedule: Day shift Evening shift Work Location: In person Expected Start Date: 17/07/2025