316 Gmp Compliance Jobs - Page 6

Responsibilities: * Ensure GMP compliance at all times * Monitor production costs & optimize efficiency * Collaborate with R&D on new product launches * Manage material planning & inventory levels Provident fund

Role & responsibilities The incumbent must have experienced working on microbial cell culture, recombinant antibody manufacturing from microbial expression systems. Should have experience in manufacturing on 1000L bioreactor and handling automated CIP, CIP and TFF systems. Experience on manufacturing of consistency and commercial scale up batches. Good knowledge of technology transfer from R&D scale to commercial plant manufacturing. Should be responsible for qualification of equipments and facility. Sound knowledge on GMP and working in close with cross functional departments for execution of manufacturing activities within specified timelines. Should lead, motivate and train the team in GM...

Job Description Summary Manages all Quality Assurance activities associated with the product development and product support processes in BD TCI. Ensures that all Design Control quality elements are established and documented to provide a safe and effective product that meets customer needs. Lead evolution and improvement of the product development process, policies and procedures which will enable design teams to respond rapidly to customer needs. Runs multiple projects directly while managing other quality engineering resources running separate projects. Provides leadership, quality oversight and direction, scheduling, decision-making, problem-solving and team-building capabilities. Mainta...

Job Title: Production Executive No. of Positions: 2 Company Name: The South Indian Manufacturing Company Company Website: www.saibol.com Location: Madurai (Local candidates preferred or must be willing to relocate) About the Company The South Indian Manufacturing Company is a reputed pharmaceutical manufacturer specializing in quality-driven processes and GMP-compliant production systems. Qualifications B.Pharm / M.Pharm / B.Sc Chemistry / M.Sc Chemistry Experience Freshers (0-2 years) are eligible Experienced candidates (3+ years) also welcome; higher salary will be offered based on profile Key Responsibilities Assist in ointment manufacturing (weighing, mixing, filling, packing, labeling) ...

Conduct regular inspections and audits of products, processes, and systems.Identify quality issues and implement corrective actions.Develop and maintain quality documentation, including SOPs and checklists.

Perform routine and non-routine quality control tests using analytical techniques such as HPLC, GC, UV-Vis, IR, titration, and others.Develop, validate, and optimize analytical methods as per regulatory guidelines.

Conduct regular inspections and audits of products, processes, and systems.Identify quality issues and implement corrective actions.Develop and maintain quality documentation, including SOPs and checklists.

Experience in Herbal extract & Vet.Products formulations. Must have knowledge o Vertical Extractor, ver. evaporator, filtration, Rotation vacuum paddle dryer, vacuum tray dryer, cooling tower, chiller, multi milling, shifter etc

Job Purpose: To lead the end-to-end operations of the cosmetic manufacturing plant, including production, planning, quality coordination, manpower management, and compliance. The role ensures that products are manufactured in accordance with GMP, hygiene standards, and regulatory norms , while optimizing cost, quality, and delivery timelines. Key Responsibilities: 1. Production Management Manage daily operations of bulk manufacturing and filling/packing lines. Ensure compliance with batch manufacturing records (BMRs) and standard operating procedures (SOPs). Monitor production metrics such as output, yield, machine efficiency, and downtime. Maintain cleanliness and hygiene in production area...

We are seeking an experienced and meticulous QA Lead to oversee all quality assurance and control activities within our food extrusion processing unit. The ideal candidate will be responsible for ensuring that all products manufactured meet stringent food safety, quality, regulatory, and organizational standards. You will lead a team of QA technicians, manage compliance systems (like FSSAI, GMP, GHP, HACCP), and be the key custodian of quality on the production floor. Role & responsibilities. 1. Quality Systems & Compliance: Manage all documentation, including SOPs, HACCP plans, PRPs, quality manuals, and batch records. Lead internal audits, third-party audits (e.g., from customers, FSSAI, c...

To check and monitor the GMP and GLP compliances. Dispatch of goods from plant - completion of all documentation and give the batch release To be responsible for overall quality assurance functions in the factory. To approve and monitor all SOPs related to QA, QC, Production, stores, Admin and Engineering departments. To approve all specifications of Raw Materials, Packing Materials, Intermediates and Finished Goods. To review and approve Validation Master Plan, Master Formula Records, Master BMR, Master BPR, Site master files. To approve and monitor all process validations, Cleaning validations, Hold Time Studies, Validations of premises, equipment and procedures. To approve the stability p...

1. Monitor raw material dispensing activity. 2. Perform daily IPQA activities as per SOP-defined frequency and ensure timely closure of IPQA observations. 3. Conduct validation sampling as per approved validation protocols. 4. Review BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) for accuracy and compliance. 5. Perform ERP-related transactions of IPQA. 6. Check BSR (Batch Summary Record) and Shipper inspection as per SOP. 7. Manage issuance, review, and reconciliation of formats across all departments. 8. Conduct IPQA rounds and share observations with concerned HODs for corrective action and compliance. 9. Ensure cleaning, sanitation, and hygiene in all departments to maint...

Role & responsibilities Designation: Sr. executive Exp.: 5-7 years Preferred candidate profile He should have understanding in Upholding regulatory compliance (GMP, ICH), Mastering robust documentation and record-keeping, Implementing quality systems like CAPA and change control, Conducting thorough internal and supplier audits, Ensuring effective quality training for personnel, Maintaining a proactive approach through risk assessment, and a strong understanding of product release processes and continuous improvement. This Is Minimum requirement for this position, eligible candidates can apply. We will schedule interview after discussion Email- ShubhamUpadhyay.Sanat@schwabeindia.com

QA Manager OSD/Liquid formulation background.Must have experience in BMR, batch release,validations,qualifications,SOPs,GMP,audits,QMS(Deviation,OOS, OOT, CAPA), tech transfer. Analytical exposure is an added advantage Resume to hrd@stedmanpharma.com

Dear Candidate: We are excited to announce a new opportunities at Nuflower Foods & Nutrition Pvt. Ltd. in our Stores department based at Manesar. This role involves end to end store operation including material receiving, issuance, dispatch & maintenance of inventory stock of materials & finished goods as per the requirements. Job details include: Designation: Senior Executive / Executive - Stores Work Location: Manesar, Gurugram Years of Experience: 4+ years Educational Background: Preferably MBA in Supply Chain Management / MBA in Operations Major role & responsibilities includes: Store Operations & Planning Manage engineering stores, capacity planning, warehousing, dispatch, and material ...

Looking for Production Chemist for Vasai Location, daily production of colour cosmetics quality control and batch consistency formulation and process improvements understanding of manufacturing processes

Hiring for Principal Scientist for a leading Pharma MNC at Pune. Role & responsibilities Reporting to : Associate Director Job Summary : To develop synthesis processes of highly potent and/or cytotoxic ADC drug-linkers and transfer processes to internal/external clients and collaborate with manufacturing teams to deliver robust chemical processes that are suitable for commercial-scale manufacturing, while ensuring safety and regulatory compliance. Key Responsibilities: 1. Detailed technical evaluation of project enquiries received from the customers/ BD team. 2. Literature search, scouting the appropriate routes, and Drug-linker process optimization. 3. Execution of Bioconjugation Chemistry ...

Technical Engineering requirements Ensure operation of all the equipment / systems in the unit / area assigned Equipments to be operated and maintained are: AHU's, Ventilation units Utilities like Chiller, Air Compressor, DG, Pumps, cooling tower etc. Pipings of all Utilities Building Maintenance and Minor maintenance of Lab equipments Ensuring Operation of Equipments as per requirement and proper documentation completion Ensure completion of all PPMs scheduled in the area in a timely manner Preparation of Annual PPM planer and schedules, review of checklist Ensuring completion of PPM on time and at actual with proper document completion Ensure response to issues / complaints on time and res...

Technical Engineering requirements Ensure operation of all the equipment / systems in the unit / area assigned Equipments to be operated and maintained are: AHU's, Ventilation units Utilities like Chiller, Air Compressor, DG, Pumps, cooling tower etc. Pipings of all Utilities Building Maintenance and Minor maintenance of Lab equipments Ensuring Operation of Equipments as per requirement and proper documentation completion Ensure completion of all PPMs scheduled in the area in a timely manner Preparation of Annual PPM planer and schedules, review of checklist Ensuring completion of PPM on time and at actual with proper document completion Ensure response to issues / complaints on time and res...

Responsible for Supporting API plant operation in shift, handling equipment like- Reactor, Centrifuge, FBD, RMG, Sifter, MCM, Blender, VSM, Filter Etc, Maintain all parameters as per SOPs, trouble shooting, compliance of GMP, EHS & ISO norms etc Required Candidate profile M.Sc./B.Sc/Dip.Chemical with 4 to 8 yrs relevant working exp in API/Bulk Drug plant. Should be well Conversant with API mfg conversion reaction & unit operation. Must have work exp of GMP compliance. Perks and benefits Negotiable

Responsible for API Plant shift Oprn like batch charging,Reaction, extraction etc, Planning& Scheduling Prodn activities, maintain parameters as SOPs, Ensure GMP regulatory/EHS & ISO compliance, troubleshooting, documentation, SAP Entry, Manpower mgt Required Candidate profile BE-Chemical with 4 to 8 yrs relevant working exp in API plant. Should be well Conversant with API mfg conversion reaction & unit operation like filtration, drying, Batch/Continuous Distillation Column Perks and benefits Negotiable

Responsible for nutrition addition, harvesting, washing, homogenization, spray drying, packing. Shall check the maintenance of the department, premises, and equipment as per SOP and GMP norms.

Production GMP coordinator To initiate change control, preparation of draft documents (Existing and proposed) of change control. To discuss the changes with QA and to take approval. To initiate investigation and preparation of OOS, OOT and deviation investigation report of respective plant and ensure timely closer of documents. Preparation of new SOP and revised existing SOP as per requirement and initiation in documentum software and to take approval. To perform daily GMP round in respective plant and ensure compliance and online documentation. Monitor the Change control, CAPA and deviation in track wise system and its tracking and closures of respective plants and ensure timely closer of d...

Assistant Manager / Sr. Executive based in Kadi, Mehsana District, Gujarat. The ideal candidate brings 5 to 10 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improveme...

Officer Production / Sr. Officer-Production based in Ankleshwar, Gujarat. The ideal candidate brings 5-8 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S...