4062 Gmp Jobs - Page 5

To ensure that all equipment in the process section (Blancher, SAPP / Dextrose System, Dryer, Fryer and Freezing) is operating to it s full potential in order to supply the production line with the required quantity and quality of specified processed cut potatoes. Recording / monitoring of both quality / processed efficiencies while ensuring area and staff are hygienically clean Instructions for Responsibilities and Accountabilities: List the major responsibilities and accountabilities of the position in order of importance with most important being first etc. Each item should describe what the person in this position have to accomplish at McCain. (i.e. what the job produces) as well as the ...

To Support QC lab for Procurement, Inward and Issuance of standards, Impurities, Chemicals, Solvents, Columns and Other miscellaneous items for analysis. Indent in SAP, Generation of IH house standards, Cordinate with GTA for inventory procurement and shipment. Job Responsibilities Coordination with respect to SOP harmonization; harmonization in specifications, test methods and formats as per Apotex Inc. and LIMS requirement. Raising Indent for required material, follow-ups and co-ordinate with purchase department, supplier, manufacturer and vendor. Co-ordinate for receipt and approval of Invoice. Co-ordinate for shipment of samples to Apotex. Shipment tracking and co-ordinate with warehouse...

Mynvax is a biotechnology company focused on the discovery, development, and scalable manufacturing of thermostable recombinant vaccines against respiratory and emerging viral infections. The company collaborates closely with leading academic and translational partners including the Indian Institute of Science, THSTI, and global R&D groups. Role Lead upstream process development for recombinant protein and vaccine antigen production using insect (Sf9, Sf21) & mammalian (CHO) cells. Plan, design, and execute experiments for media/feed optimization, infection/transfection kinetics, and process scale-up (1-50 L). Supervise and mentor a team of 4-5 Research Associates/Senior Research Associates ...

Join Thermo Fisher Scientific s PSG IT CoE at Hyderabad and help redefine how digital manufacturing powers life-changing therapies. This position is responsible for designing, developing, validating, and maintaining electronic manufacturing recipes within the Manufacturing Execution System (MES). The primary responsibility of this role is to verify the accuracy of all recipes and workflows to match current production methods and meet cGMP, FDA 21 CFR Part 11, EU Annex 11, and company quality criteria. Collaborates with process engineers, manufacturing, and IT to convert batch process requirements into approved electronic records and automated workflows. Key Responsibilities Build and configu...

Conduct laboratory tests and analyses on raw materials, in-process items, and finished products to verify compliance with prescribed standards. Prepare, label, and store samples according to protocols, ensuring safety and integrity. Record, interpret, and report test results accurately, following guidelines for documentation and traceability. Calibrate, clean, and maintain laboratory equipment, and ensure all instruments function according to quality requirements. Identify defects or deviations, document quality issues, and communicate findings with the production or management team for corrective action. Follow Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and safety st...

Roles and Responsibility Develop and implement effective business strategies to achieve organizational goals. Build and maintain strong relationships with clients and stakeholders. Analyze market trends and competitor activity to identify opportunities. Collaborate with cross-functional teams to drive business growth. Identify and mitigate risks to ensure compliance with regulatory requirements. Monitor and report on key performance indicators to measure business success. Job Requirements Proven track record of achieving business objectives in a fast-paced environment. Excellent communication, leadership, and problem-solving skills. Ability to work independently and as part of a team. Strong...

We are seeking a detail-oriented and proactive IPQA Executive to join our Quality Assurance team. The ideal candidate will ensure compliance with GMP (Good Manufacturing Practices), GDP (Good Documentation Practices), and AICOA

Responsible for planning, organizing, coordinating, and controlling production activities to meet the monthly production plan. Oversee machine qualifications and review BMR during manufacturing and after completion to ensure documentation. Perks and benefits Accommodation, Travelling Mediclaim Policy

Walk-in interview For Sun Pharmaceutical Industries Limited, Job Location: Dadra & Nagar Haveli Date: 16th November 25 (Sunday) We are recruiting for our OSD manufacturing facility located at Dadra Time: 9 AM to 5 PM Interview Venue: The Classic Verna , Plot No. U-115/A, Verna Industrial Estate, Phase II-E, Landmark : HDFC bank Verna Branch, Verna - Goa 403722 Following are the requirements for our manufacturing facility at Dadra Location. 1) Designation: Officer / Sr. Officer / Executive Manufacturing & Packing Education: B. Pharm / M. Pharm Department: OSD Manufacturing & Packing Experience: 4 - 8 years of experience in OSD manufacturing handling Granulation, Compression, Coating and inspe...

Urgently Required CSV Trainer For Part Time Basis and Online Training Sessions. Should have Experience in Computer system validation and LIMS Functional Specifications (FS)Design Specifications (DS) Validation Protocols (IQ, OQ, PQ) (FDA, EMA, GAMP 5 Required Candidate profile Experience in employing risk-based approaches to CSV Experience in qualification of GLP Instrument Systems Classes Mode Online or Remote Mode Interested Directly Please Contact - 9133469786

About the Company: Company is an end-to-end CDMO (Contract Development & Manufacturing Organization) with over 30 years of experience serving pharmaceutical and biotechnology companies. The company operates a network of many global facilities and over 3,000 professionals worldwide. One of its Indian sites is located in Hyderabad, under its global operations. Job Title: CMMS Business Analyst (Blue Mountain) Location: Hyderabad, India Employment Type: Permanent, On-site Position Overview: We are seeking a highly skilled Business Analyst specialising in CMMS (Computerised Maintenance Management System) with proven experience on the Blue Mountain RAM platform (or equivalent) within regulated pha...

About the Opportunity GLOBAL CALCIUM is a USFDA, EU-GMP and COFEPRIS approved manufacturer of high-purity Active Pharmaceutical Ingredients (APIs), including Specialty APIs, Psychotropic Antipsychotic APIs and Ophthalmic APIs. We also provide top-quality Mineral Salts and Premixes for pharmaceutical, nutritional, food and other applications. As industry leaders, we specialize in an extensive range of therapeutic segments. Our expertise encompasses Antipsychotic, Antifungals, Antidepressants, Antihypertensives, Anticonvulsants, Antispasmodics, Antiepileptics, Antiemetic, Anti-inflammatory, Antiglaucoma, Antibacterial and Hematinic medications and more. Role Responsibilities Operation maintena...

Job Summary To implement efficient, quality processes at ARPL in alignment with global standards that comply with heath authority requirements. Responsible for monitoring of activities related to Product Market Complaint System Internal and Vendor audit management Supplier Management Quality Agreements Artwork Management Nitrosamine assessment and management. People Management Job Responsibilities Responsible for handling Health Authority Inspection. Ensure adherence to GMP regulatory requirements by one and all in the facility. Responsible and accountable for competently managing subordinates and to provide all required training, equipment, tools and follow procedures in accordance with app...

1.Preparation and standardize of volumetric solutions and maintaining its record. 2.Preparation of standard solutions and reagents and maintaining its record. 3.Water Analysis and data punching in SAP. 4.Analysis of Raw Material and Miscellaneous samples as per GTPs/ SOPs/ Spec MOAs. 5.Raw materials Control sample management. 6.To put results in SAP of analyzed and Reviewed RM Materials. 7.To Record Maintain temperature record of entire QC lab on daily basis. (except Microbiological and PM testing QC). 8.To Check Refill Eye washer equipment on daily basis and Record data of the same.

Join us as a Trade & Transaction Reporting Manager Well look to you to provide oversight on daily trade and transaction reporting processes, making sure that they adhere to the control framework and comply with regulatory obligations Youll provide input into regulatory reporting initiatives, through your expertise and knowledge of regulations, data analysis and issue remediation As a key member of our team, youll enjoy extensive collaboration and can expect great visibility for you and your work We're offering this role at vice president level What you'll do As a Trade & Transaction Reporting Manager, youll be operating a robust oversight model of trade and transaction submissions to support...

We are hiring an experienced Analytical R&D professional with expertise in ICPMS ICPOES for method development and validation The candidate should have hands-on experience in elemental impurity analysis, instrument handling, and GMP GLP documentation

Ensures that the review of CMC documentation is completed in timely compliant manner as per Teva CORP standards and related Guidances. Review of Method Development/Validation Protocols Reports, Stability Protocols Reports received from various Teva contracting sites, RD units, Method Development Stability Testing Centres. Review of Instrument/Equipment Qualification records. Review of BMR. Ensures that the Product Quality Reviews / Annual Product Reviews for Teva products are completed in a timely and compliant manner as per Teva s CORP Quality Management systems. PQR/APR compilation and approval must be we'll associated with the Teva Manufacturing Sites, Global Quality Units and Commercial ...

Role & responsibilities 1. Beverages experience is mandatory. 2. We are a high-speed non-alcoholic beverages (CSD/juice/water) PET bottling plant. 3. Applications without hands-on beverages bottling exposure (PET filling/blow-moulding/syrup room/CIP) will not be processed. 4. Kindly do not apply if your background is primarily dairy, brewery/alcohol, pharma, chemicals, snacks/foods without non-alcoholic beverages bottling experience. 5. Then add crisp responsibilities and the equipment list (filler/BFC/BLOW/labeller/packer/palletizer) so non-beverage candidates self-exclude. Preferred candidate profile Location: Bardoli - Surat Experience: 310 yrs Industry: Beverages /Soft Drinks Functional ...

Job Title: Formulation ADL - Analyst Division Integrated Product Development Department Global Respiratory Job Purpose Execute the core method development activities and conduct analysis of routine as well as stability samples to finalize specifications and ensure timely delivery of product to unit. Key Accountabilities (1/6) 1.Develop new analytical methods for analysis of routine as well as stability samples by following proper GLPs to provide results or information regarding products to formulators 2. Perform maintenance and calibration of lab instruments / equipment to get accurate and reproducible analytical result for proper interpretation 3.Document and interpret the analytical data i...

Job Title: PQMS / FSMS Coordinator Location: Ranchi, Jharkhand Reporting To: QA Manager / Plant Head Job Purpose: To ensure effective implementation, monitoring, and continual improvement of Product Quality Management System (PQMS) and Food Safety Management System (FSMS) as per company standards, FSSC 22000 / ISO 22000 requirements, and applicable statutory norms. Key Responsibilities: 1. Documentation & Compliance Prepare, update, and control PQMS & FSMS documentation (SOPs, manuals, forms, records). Ensure compliance with FSSC 22000, ISO 22000, HACCP, and related standards. Maintain updated records for audits, inspections, and certifications. Support in external audits (FSSC, ISO, custome...

Job Title: PQMS / FSMS Coordinator Location: Ranchi, Jharkhand Reporting To: QA Manager / Plant Head Job Purpose: To ensure effective implementation, monitoring, and continual improvement of Product Quality Management System (PQMS) and Food Safety Management System (FSMS) as per company standards, FSSC 22000 / ISO 22000 requirements, and applicable statutory norms. Key Responsibilities: 1. Documentation & Compliance Prepare, update, and control PQMS & FSMS documentation (SOPs, manuals, forms, records). Ensure compliance with FSSC 22000, ISO 22000, HACCP, and related standards. Maintain updated records for audits, inspections, and certifications. Support in external audits (FSSC, ISO, custome...

Job Title: Sr Recruiter - (Healthcare Manufacturing/ Medical Device) Location: Vastrapur, Ahmedabad Shift Timings: 7:00 PM to 4:00 AM (U.S Shift) Mon - Fri 100% Onsite Role Experience Required: 1 4 years Job Summary: Specializes in recruiting for medical device design, engineering, quality, manufacturing, and regulatory roles. knowledge of GMP/FDA/ISO standards. About the Role: 14 years of full-cycle recruitment experience in medical device, healthcare, or pharmaceutical industries. Proven experience supporting clients such as Boston Scientific, Medtronic, DaVita, Abbott, Stryker, or similar. Strong understanding of GMP, FDA, and ISO 13485 environments. Proficiency with ATS systems (JobDiva,...

We are seeking a highly skilled Formulation R&D professional to lead the development of oral drug delivery systems , primarily focusing on soft gelatin capsules, tablets, and sachets . The role involves driving end-to-end formulation development, process optimization, and technology transfer from lab to commercial scale. The incumbent will be responsible for conceptualizing and executing formulation strategies, troubleshooting technical issues, and ensuring successful product development aligned with regulatory and GMP standards. The position requires close collaboration with cross-functional teams including analytical R&D, manufacturing, and regulatory affairs, while also contributing to in...

This job is with Pfizer, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Use Your Power for Purpose At Pfizer, our mission is to cultivate a best-in-class culture of continuous improvement and project management that empowers colleagues and streamlines processes. Whether you are managing projects or collaborating with others, your role in this team is crucial in making our work more efficient and effective. By simplifying and enhancing our processes, we can deliver breakthroughs that transform patients lives. Your contributions will help us achieve our goal of making our work easier and...

As a Facility Executive, you will be responsible for overseeing the preventive maintenance, compliance, and operational efficiency of the facility. Your role will involve managing service contracts, ensuring equipment reliability, and maintaining safety and regulatory compliance. The ideal candidate for this position should have experience in facility maintenance within the food industry and be well-versed in GMP, HACCP, and environmental regulations. Key Responsibilities: - Develop and implement preventive maintenance schedules to ensure minimal downtime and food safety compliance. - Monitor and update maintenance Standard Operating Procedures (SOPs), job plans, and records for audits. - Ut...