316 Gmp Compliance Jobs - Page 11

Bombay Ortho Industries Private Limited (A wholly owned subsidiary of Alkem MedTech Private Limited) Job Description Overall responsible for conducting all EHS related activities at site and allied business facilities including Ensuring effective implementation of sites Occupational Health, Safety and Environment Policy Ensuring implementation and documentation of Occupational, Health & Safety Management System and elements thereof Ensuring implementation and documentation of Environmental Management System and elements thereof Ensuring compliance with EHS related statutory provisions including Act, Rules, Notifications, Directives etc. including liaison work, renewal of Consents and EHS rel...

Should have Knowledge of Documents. Should able to handle skilled/unskilled Labour. Should have knowledge of GMP/GDP Practice & aseptic behaviour. We are looking for pharma background candidate only. Perks and benefits PF Bonus Food

Key Responsibilities: (Quality Executives) Monitor and maintain quality standards across production stages Conduct routine lab tests and ensure product compliance Supervise hygiene, sanitation, and food safety protocols Handle customer complaints and implement corrective actions Maintain all QA documentation and regulatory records Train production staff on quality systems and SOPs Coordinate with production, maintenance, and procurement teams Participate in internal and external audits Key Responsibilities: (Packing & Processing Operator) Operate and monitor dairy processing and packing machinery Ensure correct packaging of milk and milk products as per standards Maintain hygiene and cleanli...

Dear Candidate , we are hiring for the Position Jr Executive .(Instrumentation,Hematology,Activity,Potency Based Assays,Bio chemical group) 1.Candidate have good hands on experience in HPLC, electroscopic test methods. 2.should be able to handle liquid chromatography instrument and relevant 21 CFR softwares 3.should be able to handle ELISA Reader ,microscope,basic QC Instruments . 4.candidate should have good hands experience in colorimetric ,spectrophotometric. 5. should be have a idea on GLP compliance requirements. for more details please reach out Venkat -9381915043 /Manasa - 9502434725

Job Title: Officer/Senior Officer Location: Ankleshwar Experience: 2-5 Year Department: Production Role and Responsibilities: Production Operations Check labels and verify identity of raw materials, packing materials, and solvents before use. Maintain appropriate storage conditions for raw materials and intermediates in the plant. Execute batch processes as per approved Batch Production Records (BPRs). Follow instructions from Shift In-charge or Production Manager for batch charging and monitoring. Monitor and maintain process parameters during manufacturing. Complete allocated tasks within the stipulated timeline with accuracy. Ensure contamination-free production and proper packing/repacki...

Roles & Responsibilities: Daily R.M. /P.M. planning and issuing as per production schedule. Manpower allotment in shifts and to give and take proper shift charge from reliever. To review BMR, BCR, documents and to submit to QA. To check the processing is being done as per instructions written in BMR. To report any kind of deviation/abnormal incident to HOD immediately. To ensure safety, GMP, discipline & housekeeping in plant. To ensure that all production related documents are filled on line & accurately. To give training to subordinates, prepare and maintain training related all activity and documents. To prepare, issue and submit all documents like BMR, BCR, SOP etc. as draft for producti...

QA Head Seeking a QA Head to ensure skincare products meet regulatory, safety, and quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 4+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to train & improve Jr.

Ensure machine availability to production to achieve monthly production targets. Ensure effective preventive maintenance programme to minimize machine breakdowns and to increase machine operational time. Ensure that highest standards of safety are being followed for all engineering related activities Support the cross functional teams for specific projects and activities like Lean Management, validation activities etc. at site. To raise Change Requests, Planned Deviations and Exceptions in system. To track and complete all QMS (Quality Management System) related activities. To verify all records related to QMS activities. To ensure that best Engineering & GMP practices are being followed whi...

Role & responsibilities : ISO 9001/ISO 13485. Manage the Quality Management System. To provide QA support in all quality related matters and to ensure that all aspects of the operational business comply with cGMP legal and regulatory requirements. Risk Management & CAPA. Establishing procedures and records as per requirement of standards and regulatory authorities. Responsible for establishing, managing, and implementing Records Management policy, Records. Retention and retrieval procedures are in place. To manage and execute internal and external audit schedules and follow up on action plan, Quality Auditing of External suppliers - maintain an annual auditing program. Regular Internal Quali...

Roles & Responsibilities: Associate Manager Responsible for shift activities Responsible for extension of method Validation/ transfer Responsible for review of the analytical report Responsible on need basis in line with the requirements day to day basis Senior Executive Responsible for analysis of Raw Material In process, Intermediate finished Products using GCP, HPLC, IR, Potentiometric Responsible for calibrations, WS Generation and lab readiness for audits Responsible for GMP/GLP procedure in QC Lab Executive Hands on Experience on Trouble Shooting Knowledge in PH Meter/KF/ Potentiometric Exposure in Regulatory audits Good Documentation practice Preferred candidate profile Male Candidate...

Roles :- * Knowledge of cosmetic and personal care product manufacturing processes (e.g., mixing, filling, emulsifying, packaging) * Understanding of GMP and regulatory compliance * Familiarity with batch processing, SOPs, and quality documentation

The job involves preventive maintenance of production equipments and utilities (chiller, blowers, HVAC etc), coordination for validation of equipments, maintain GMP compliances, participate in new equipment installations, general maintenance of buil

Role & responsibilities Key Responsibilities: Strategic & Policy Development: Define, implement, and continuously improve QA/QC policies, procedures, and standards aligned with global best practices (e.g., ISO, GMP, Six Sigma). Develop strategic quality plans in alignment with organizational objectives. Team Leadership: Lead and manage the QA/QC team, including hiring, training, mentoring, and performance evaluation. Foster a high-performing team culture with a strong focus on accountability, results, and continuous improvement. Quality Management System (QMS): Monitor and improve the organizations QMS to ensure effectiveness and compliance with applicable standards. Lead quality system impl...

Job Title: FDA & International Pharma Compliance Consultant (Excipients, API & Ingredients & Formulations) Location: Kutch, Gujarat (Remote advisory with periodic on-site presence) Experience: 2025 years in pharmaceutical manufacturing and regulatory compliance Salary: Competitive Education: Bachelors or Master’s in Pharmacy, Pharmaceutical Sciences, Chemistry or related discipline Kindly get in touch for career advancement opportunities with us at rupsha.saha@antal.com Roles & Responsibilities Guide the upgrade and development of plant infrastructure and systems to achieve compliance with: WHO-GMP Regulatory requirements of Russia, Australia/New Zealand, African authorities Ultimate readine...

Roles and Responsibilities Ensure compliance with GMP guidelines during API manufacturing processes. Monitor equipment performance and troubleshoot issues related to piping systems. Maintain accurate records of production data, quality control tests, and inventory management. Experience needed: Production - 0 -4 years Engineering production-6-8 yrs

Reporting to Sr. Director - Regulatory Affairs Experience required: 5-8 Years Education: B. Pharm / M. Pharm Department: Regulatory Affairs Key Responsibilities: Prepare the status of all documents related to submission. Compile and review Regulatory submission documents required in line with the relevant guidelines. Coordinate with all stakeholders of the manufacturing plant for the collection of documents. Evaluation of change control: evaluate all post-approval changes. Review of specifications (API, Intermediate, FP, and Shelf life) executed BMRs, BPRs, COA, Method transfer report, Method verification, Analytical chromatograms intended for regulated or non-regulated market submission. Ge...

Role & responsibilities Ensuring compliance to GMP during day-to-day activities on shop floor. Review of day-to-day and online compliance. Performing SAP transaction as required. Timely performing sampling at different stages as per the requirement. Ensuring and giving clearance for various stages during day-to-day activities like, Line clearance in Dispensing, Mixing, Autoclave, Washing, Depyrogenation Tunnel, Filtration, Filling, Terminal sterilization, visual Inspection, labelling, packing. Collection of various samples as per the requirement. To review of GMP document. Identification of deviation through review and observation. Handling over the shift base change for continued operation....

We are looking for Quality Head, who has worked at least 10years in SGI Casting speciality in Manhole cover division. Maintain QMS, with computer knowledge. Job location-Howrah(WB),Salary-35k-45k Monthly. Walk in Interview. Contact : +91 7687919790

Role & responsibilities Handling and management of the Engineering department. Overall responsible for the maintenance of the plant, Machinery, Utilities, Building, and premises Coordination with concerned department heads for the timely execution of engineering activities. Planning and scheduling preventive maintenance of Production, QC, Warehouse equipment, and utility as per the preventive maintenance planner. Review of SOPs, protocol & reports, and preventive maintenance planner and checklist. To provide technical guidance to the engineering team and top management. Responsible for the selection and design of equipment, plant layout, materials handling, and ordering of material. Up-datio...

Open Positions: Officer / Executive / Sr Executive Quality Assurance & Quality Control : Analytical Skill on HPLC, Electrophoresis, Microbiology, Document Review, IPQA, Quality Systems, GMP Compliance, QA-QMS Biosimilars Manufacturing: Downstream (Operation of Chromatography systems) & Upstream (Handling of Single use and Stainless-steel bioreactors) Experience: 2 to 10 years of relevant experience in Biopharmaceutical Qualification: B Sc / B. Pharm/B Tech / M Sc in Microbiology / Biotechnology / Chemistry/M. Pharm Date : 01st June 2025, Sunday Time : 08:30 AM to 06:00 PM (Registration will be closed by 12:00 PM) Venue : Hotel Pride , 5, University Rd, Narveer Tanaji Wadi, Shivajinagar, Pune...

Responsible for aligning production schedules with demand forecasts, optimal raw material availability & minimizing downtime & inventory costs Coordinate with production, R&D, QA/QC & procurement teams to ensure timely & efficient batch planning Required Candidate profile 6–8 years in production planning and control (PPC) in specialty chemical or polymer manufacturing Strong understanding of Batch Manufacturing, EHS, GMP & compliance protocols ERP Software is must

Roles and Responsibilities Ensure compliance with EHS regulations, policies, and procedures at API manufacturing facilities. Provide training on EHS best practices to employees at all levels within the organization. Develop, maintain, and update safety documents such as SOPs, risk assessments, and incident reports. To ensure safety in process plants / sections in shift, by on the job monitoring /CAPA. Issuing of the work permit's with verification of job, Supervision & monitoring. To operate ETP in shift & ensure discharge of treated effluents as per MPCB norms. To maintain in order all PPE's, FFE's, SCBA's, OHC, MCP's, Fire water pumps, safety shower, smoke detector etc. Desired Candidate P...

The Junior Executive – Warehouse will support day-to-day operations within the warehouse to ensure the proper handling, storage, and dispatch of pharmaceutical products in compliance with regulatory and company standards. The role involves inventory

Job Objective - Maintain machine continuity, quality of production, reduce wastages and adherence to cGMP in-shift for the allocated machines. Roles and Responsibilities - Check the allocated machine in each shift as per the CTQ (critical to Quality) checklist (Machine checking report), pin lubrication monitoring. Blade change, jaw/cheek change, collet change) under the supervision of Shift supervisor Dip Bath, greaser, blade, Replacement of dome wiping felt and oiling, collet oiling and cleaning as per SOP. Colour change (removal and insertion of dip bath, machine cleaning) as per SOP Attending tripping on HCM and bring the machine back to running condition. In certain cases, seek help from...

NOTE : IMMEDIATE JOINERS ARE PREFERRED 1) Receive different kind of PR and requirement from different department (Production Consumables, Microbiology, BT, R&D, QC, Russia Project, Maintenance (Asset, Domestic, Import, Service), Pharmacopeias of RA from our End User. 2) Source Vendors according to material and float enquires for the quotation. Minimum 2-3 quotes require for comparison. 3) After getting the quote, take technical confirm with our end user and check all the technical points of quotation like delivery time, payment terms, warranty, inclusion, exclusions etc. 4) Discuss and negotiate with vendor for the best price and delivery time of material. 5) Accordingly prepare comparison s...