4089 Gmp Jobs - Page 26

Pharma manufacturing, Quality Assurance, Quality Control, GMP, GLP, HPLC, SOP, Validation, Regulatory Documentation, Production Supervision. For further information, please call -7026629008 / 8050011327

Research & Development / Quality Assurance / Production

Trainee - Operator: Educational Qualification - Diploma in Engineering (Mechanical/Electrical/Electron ics) Experience - 0 - 3 years experience of operating pharmaceutical manufacturing machines in Ointment & Liquid section Job Responsibilities - To operate machines related to manufacturing andpacking activities of Semi Solid Dosage(Ointment), ExternalPreparations & Liquid oral. To adhere with cGMP & SOP Compliance in the department and ensure safety & quality ofproduct during manufacturing & packing operation To achieve desired production targets, control of wastage and yield improvement during process operations. To do online in process checks and donecessary entries in BPR at regular inte...

Handling Customer Complaints, Change Control, Deviation, CAPA, Customer Audit / Visit, Product re-call, Leading the Quality team from the front, Accountable for QA/QMS/QC & Micro complete operations etc. Working knowledge of IPQA & Clients SOP & QMS

Location: Gujarat, GJ, IN, 382845 JRS India Corporation Private Limited is a wholly owned subsidiary of the J.R. Simplot Company. The J.R. Simplot Company is a diverse, privately held organization, with roots firmly planted in agriculture and agriculture-related businesses. The J.R. Simplot Company is a true farm-to-table company with operations that touch every aspect of agriculture, including seed production, farming and ranching, plant sciences, fertilizer manufacturing, food processing, commercial product development, and distribution. Summary Tends, maintains, and adjust machine that stock, fill, wrap, seal and label bags with finished product. This individual ensures that product and b...

Job Title: New Product Development Trainer Location: Remote Job type: Part -time Job Summary: We are seeking an experienced NPD Trainer with over a decade of hands-on expertise in medical device design, product development, validation, and regulatory compliance . The Trainer will be responsible for designing and delivering structured training programs to upskill engineers, technicians, and project managers in end-to-end new product development processes from concept to commercialization. The ideal candidate should possess strong technical depth, familiarity with ISO 13485, FDA 21 CFR Part 820, and Design Control requirements, and the ability to translate complex product development concepts ...

Responsible for document management like BMR s, BPR s, master SOP s etc. Responsible for preparation & review of the master documents of production. Responsible to ensure UAF working in area. Responsible for the handling of change control, deviations, investigation & CAPA, etc Responsible to give training to all the subordinates, technicians and operators of the department. Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HOD s instruction and guidance. Responsible for line clearance activity before commencing the operations. Responsible to check that all the records and logbooks related to aseptic manufacturing, vial filling...

As a Mechanical Engineer, you ll be working with an innovative, multi-disciplinary team where you ll be supporting or leading following tasks: Dimensioning and specification of mechanical equipment e.g. heat exchangers, pumps, agitator selection etc. Dimensioning and specification of auto & manual valves, relief/ Safety devices, control devices, pipes and in-line components. Perform flow analysis Specification and design of Tank and Vessels Vendor/ supplier /client / cross disciplinary coordination and perform/ participate reviews (Disciplinary and cross disciplinary) Handling purchase and supplier contract Executing projects in the construction phase using supervision and supervise of contr...

Plans, schedules, coordinates and/or monitors final approval of products through the complete production cycle. May be responsible for the following activities: master scheduling, production planning/coordination, distribution planning, dispatching, co-ordinating with warehouse team, material requirements, planning systems, work-in-process tracking. Changes to individual responsibilities may occur due to business needs and other related duties may be assigned. Scope of Responsibilities: Applies core knowledge and understanding of area of specialization to provide solutions in creative and effective ways. Assesses unusual circumstances and uses sophisticated analytical and problem-solving tec...

Sberbank is looking for a Senior Business Development Manager to join our expanding team in Delhi. This pivotal role focuses on driving growth and expanding operations within India's FMCG and consumer goods sector, with a strong emphasis on supplier strategy, cross-functional collaboration, and international business development. Responsibilities Conduct supplier sourcing activities for raw materials, packaging, and logistics in a timely and efficient manner. Manage the supplier sourcing process, including identifying potential partners, evaluating their capacity and compliance, and selecting the best fit. Build and maintain strong supplier relationships across FMCG categories (food, persona...

Job description Based on recruiter search Roles and Responsibilities : Conduct quality control tests on pharmaceutical products using HPLC, GC, UV, and other analytical techniques. Ensure compliance with GMP guidelines and regulations by performing

This role supports that R&D Quality Assurance organization with know-how in GMP, Quality Control, Analytical Development, and management of stability programs. Principle Responsibilities: Quality Assurance Oversight of Internal R&D Laboratory: Provide Quality Assurance oversight to the laboratory, manufacturing, and analytical control activities of R&D Laboratory in Hyderabad Oversee laboratory change controls, investigation reports and incidents for their timely closure Oversee of Stability Chamber s data logs and reports review. Issuance of laboratory Notebooks (LNBs) and Usage Logs and retrieval/archival of documents (LNBs, Usage Logs, calibration documents, raw data files, qualification ...

Routine Chromatographic analysis: Responsible to perform analysis for UPLC, HPLC, GC, GC-HS-MS, ion chromatography & Chiral analysis of GMP Pilot plant, Scale up and Other R&D samples. Routine Wet analysis: Responsible to perform analysis for routine chemical analysis of samples comes from GMP Pilot plant, Scale up and Other R&D samples. Calibration: Perform the daily and monthly calibration of instrument as per the calibration planner. Raw material: Responsible for raw material analysis of different GMP Pilot plant, Scale up and Other R&D projects. Qualification: Post Graduate in Science. Experience: Working knowledge of HPLC, GC, IC & Wet analysis.

Experience Required: 3 5 years in QA in the food industry with hands-on FSSC 22000 implementation and audit experience Job Summary We are looking for a proactive and knowledgeable QA Head to lead the Quality Assurance function at our flour milling facility. The ideal candidate will have proven expertise in implementing, maintaining, and auditing food safety and quality systems such as FSSC 22000 and HACCP . This role will be responsible for ensuring regulatory compliance, managing audits, building a quality-driven culture, and serving as the interface between the company and customer QA teams. Key Responsibilities 1. Quality Systems & Compliance Lead the implementation and ongoing maintenanc...

As Senior Food Technologist, you will own the full product lifecycle from concept to regulatory POV, drive innovation with new formulations, optimize quality and cost of existing SKUs, and ensure all products are best-in-class and fully compliant.

Laboratory Testing Conduct daily tests on wheat and flour (moisture, ash, gluten, falling number, farinograph, extensograph, etc.) Ensure accuracy, SOP compliance, and equipment calibration Report deviations and support root cause analysis Application Trials Execute baking trials (bread, biscuits) for flour performance validation Document trial data, simulate customer conditions, and support product development Documentation & Records Maintain lab registers, test reports, sample logs, and traceability Help prepare Certificates of Analysis (COAs) for dispatches Support QA Team Assist in audits, complaint investigations, and validation exercises Follow GMP, GHP, and FSSC food safety protocols ...

Review of Audit Trail for Chromatographic & Non-Chromatographic Systems. Ensure implementation of relevant quality policies, standards and procedures for computerized systems. To review and identify gaps of Global Quality Standards/Global Standard Operating Procedure with Site SOPs. To implement the Global Quality Standards/Global SOPs at site. To prepare the Departmental Annual Training Planner and tracking for the same. To work as Departmental Training Co-ordinator for Learning Management System. Overall responsible for training activities for QA Department. To review the SOPs of all departments before approval. Update data in master drive. System GAP assessment/GMP Trending/escalation/sho...

Execute all Engineering operation as per established ARPL standards and procedures. Execute in co-ordination with the user departments for maintenance issues / problems and ensuring completion of maintenance request for ARPL utility Systems. Executing / supervise with help of contactor s on daily basis for follow up and completion of maintenance activities related to Water, HVAC, Compressed Air, Chiller, Boiler, AC and other utilities. Ensuring and maintaining Engineering inventory management / up keep of minimum stock availability for Engineering spares. Providing all required utilities / maintenance support to ARPL as per the departments requirements without any breakdown and operates in f...

Handling of Change control, Handling of Deviation and CAPA management system, Handling of Internal and external audits, Sound knowledge about Equipment and Utilty qualifcation, Should have thorough understanding about regulatory guidelines, cGMP norms, GLP, GDP, Data integrity requirements etc. Should have experience of regulatory audits.

Oversight of all production and testing activities, ensures compliance with cGxP, incl data integrity and eCompliance -Support exception investigations -Review and approval of production, QC, and AS and T records -MBR review -Support OpEx improvement projects Qualified Person Executes batch release in compliance with registration -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable) Essential Requirements On-time and GMP-compliant release of dosage forms -No complaints about inspections by authorities in your own area of responsibility without these being notic...

Title: Corporate Quality Projects - LIMS Business Unit: Corporate Quality IT Job Grade Executive / Sr. Executive Location: Vadodara Key Responsibilities At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Position Summ...

Sr. Planner (Distribution Planning) Manyata - Bengaluru, India Position Summary: Plans, schedules, coordinates and/or monitors final approval of products through the complete production cycle. May be responsible for the following activities: master scheduling, production planning/coordination, distribution planning, dispatching, co-ordinating with warehouse team, material requirements, planning systems, work-in-process tracking. Changes to individual responsibilities may occur due to business needs and other related duties may be assigned. Scope of Responsibilities: Applies core knowledge and understanding of area of specialization to provide solutions in creative and effective ways. Assesse...

Job Summary We are looking for a proactive professional for multifaceted role responsible for ensuring EHS compliance, EM strategy, internal audits, and managing MIS for external manufacturing. The position supports the organization s commitment to safe, sustainable, and compliant operations across EM facilities by ensuring that all third-party manufacturing partners comply with the organization s environmental, health, and safety standards, as well as applicable local and international regulations, while also ensuring data integrity and continuous improvement through structured audits and reporting. Job Responsibilities Scheduling and performing EHS audits of external manufacturing (EM) sit...

Job Purpose: To operate and maintain bottle packing machinery efficiently and ensure proper packaging of products as per GMP and quality standards. Key Responsibilities: Operate and monitor bottle packing machines (e.g., bottle unscrambler, filling, capping, labeling, and cartooning). Perform line clearance and machine changeover activities as per SOP. Ensure adherence to batch packing record (BPR) documentation requirements. Check and verify the correct packing materials as per the product batch. Maintain cleanliness and hygiene in the packing area as per cGMP norms. Coordinate with maintenance team for timely resolution of breakdowns. Conduct in-process quality checks and report any deviat...

Your key responsibilities Actively contribute to the IT applications project management initiatives that includes Validation activities as per GAMP Life Cycle approach Integrate technology with business process transformation programs like SAP, LIMS, ELN, MES, Documentum, TrackWise, Veeva Vault, ValGenesis, Argus, Regulatory Information Management System etc. Troubleshoot IT application related issues and suggest recommendations for solutions in consultation with relevant functions. Perform Gap assessment and Remediation procedures for legacy applications to ensure validation policies is in line with Life Cycle Approach Perform Software classification, IT risk assessment and Mitigation strat...