338 Batch Manufacturing Jobs

experience in Vaccine or Biosimilar manufacturing Strong exposure to In-Process Quality Assurance & Quality Management Systems and review system Knowledge of GMP guidelines and documentation practices fast-paced, regulated environment Perks and benefits 5- days working, Pf , health insurance

We are hiring people for sterile /injectables/opthalmic production roles at multiple levels Required Candidate profile Should have worked in injectables, opthalmics manufacturing companies

Responsible for executing and involving in plant activities. Update the documents likes Batch Manufacturing record, equipment cleaning record, daily checklist in online. Follow the standard operating procedure while performing the activities. Follow the In-charge instructions and execute the batches as per production plan. Before starting the batch, ensure the raw materials quantity availability and the packing intactness. Before the process ensure the equipment conditions to inline the operating procedure and process requirements. Any discrepancies observed in the process, procedure or safety should be reported immediately to the relevant reporting authority. Coordination with service depar...

JOB DETAILS 1.Perform laboratory tests to produce chemicals according to established standards and guidelines. 2.Handle laboratory equipment and supplies safely and effectively. 3.Document laboratory activities for reference purposes. 4.Monitor and report progress of analytical tests to Supervisor on a regular basis. 5.Work with Supervisor to set objectives and milestones. 6.Coordinate prioritize and plan lab tasks to meet deadlines. 7.Record and report test results to Supervisor. 8.Ensure final product meets quality and customer specifications. 9.Train junior chemists on test procedures. 10.Maintain sufficient stock of chemicals and supplies to perform lab experiments. 11.Ensure that materi...

Responsibilities: Operate and monitor vial filling, sealing, and washing machines in the injectable section. Ensure aseptic conditions are maintained during all operations in the cleanroom. Perform routine cleaning and sterilization (SIP/CIP) of equipment. Handle line setup, changeover, and minor troubleshooting of filling machines. Record batch manufacturing and equipment log sheets as per GMP guidelines. Follow safety and quality standards as per regulatory requirements (cGMP, WHO, etc.). Coordinate with maintenance and QA for smooth production activities. Required Skills: Logical thinking. Organizing. Good in communication. Required Qualification: - ITI/D.Pharm/B.Pharm

We are hiring for Multiple position in Production Department at Goa for Bangalore Location. Interested Candidates can walk in on 9th Nov 2025 or apply for this position Date & Time 09 th November ,2025 (Sunday). Time: 9.00 AM TO 5.00 PM. Note: • Contact person Mr. Srinivasa M, those who are unable to attend the interview are requested to forward their resumes to email id: naveenkumarp@microlabs.in • Candidates are requested to carry their copies of Resume, Mark Sheets,Experience Certificates, Latest salary certificate, pay slips of three months andone photographs. • If any queries call us on: 080-27839033, 34 & 38 Production: 1. Position: Asst.Manager / Dy.Manager / Manager Qualification: B....

Role & responsibilities 1 Preparation of standard operating procedure. 2 Preparation of quality documents. 3 Initiate / review of change control system. 4 Initiate / review of deviation. 5 Initiate / review of CAPA. 6 To control, issue, retrieve, retention and disposal of GMP documents as per standard procedure. 7 Review of MFR/BMR/BPR/ECR. 8 Review of validation protocols and report. 9 To participate in investigation of OOS for RM/intermediate/FP. 10 To participate in market complaint handling. 11 Review of vendor qualification documents. 12 Review of executed manufacturing and analytical records. 13 Preparation of annual product quality review. 14 To take plant round and ensure compliance ...

Responsibilities: Monitor manufacturing and packaging processes, including line clearance and in-process checks (IPQA) Manage documentation activities, including DOC-QMS systems, SOP preparation, deviation handling, and change control Support Technology Transfer (TT) activities by reviewing protocols, executing processes, and coordinating between R&D and manufacturing teams Ensure compliance with 21 CFR Part 11 requirements through validated software systems for electronic records and signatures Execute equipment qualification (DQ, IQ, OQ, PQ), process validation, and cleaning validation activities Utilize automated quality systems and digital platforms for manufacturing documentation Mainta...

Role & responsibilities Chemical Batch Process ( Production ) Preferred candidate profile Plant Commissioning, having good knowledge of DCS and DCS Commissioning in New plant.

Maintaining good housekeeping and cGMP in shop floor Preparation of New documents like BPCR and SOP Deviation , change control, OOS, activity and is compliance Plant keeps ready for audit Overall responsibility of cGMP Production should be achieved as per target. Equipment cleaning Log book and Solvent log Book to be maintained. BPCR arrangements for running batches. Review and completion of all documents like BPCR, Equipment logbook, and format as per SOP

Role & responsibilities -To perform the manufacturing process of products and to fill all the quality records in shift as per GMP. (BMR/BPR/ECR/Log Books/etc.) Following the SOP. -To give the requisition for Raw material/Packing material to Raw material store and verification of the same after receipt. -To give requisition for any consumable items to engineering store and verification of the same after receipt. -To give requisition for forms / formats and other quality related documents to QA and submission of the same to QA. -To make sure that all production deviations, non-conformance & accidents are reported along with investigation report. - To schedule training of plant personnel on SOP...

Amneal Pharma Walk-in Drive @ Pharma-SEZ, Matoda, Ahmedabad, (Gujrat) for Production/Packing department (Injectable/ Sterile) on 2nd November 2025 (Sunday) We are looking for suitable candidates for injectable/ sterile manufacturing-Packing units for Ahmedabad location. Interview Details: Date: 2nd November, 2025 (Sunday), Time: 09:00 AM to 05:00 PM Interview Venue : Amneal Pharmaceuticals Pvt Ltd Plot No 15, 16, 17 Pharmez | Village: Matoda | Sarkhej Bavla Road | Ahmedabad | Gujrat Office- (079) 2714677531 JOB LOCATION: Ahmedabad (SEZ Matoda) REQUIREMENT FOR INJECTABLE MANUFACTURING/ PRODUCTION/PACKING DEPARTMENT Designation : Operator/ Officer/ Sr. Officer /Executive/ Sr. Executive Departm...

As a member of the API Production team at Piramal Pharma Solutions, you will be responsible for strictly following cGMP, Safety, and Environmental Practices. Your key responsibilities will include: - Filling Batch Manufacturing records and equipment cleaning records - Following Good Manufacturing Practices during operations - Ensuring Good Housekeeping in the respective plant area and its equipment - Using Proper personnel protective equipment as per requirements - Planning and ensuring RM availability for daily production as per the production plan - Maintaining documents like Issue and dispensing register - Carrying out the process as per BMR without any deviation - Ensuring adherence to d...

Job Purpose: To operate and monitor granulation equipment and processes in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality pharmaceutical granules for tablet or capsule formulation. Key Responsibilities: Operate granulation equipment such as high-shear mixers, fluid bed dryers, oscillating mills, and blenders. Weigh, dispense, and mix raw materials as per batch manufacturing records (BMR). Monitor granulation parameters and adjust settings to maintain product quality. Perform in-process checks (e.g., moisture content, granule size) and document results accurately. Clean and maintain equipment and work areas as per SOPs. Execute machine changeo...

Role & responsibilities : Production Planning: Manage daily manufacturing activities, manpower, and ensure timely, quality production as per schedule. Documentation & Compliance: Complete and review BMRs, follow SOPs, and ensure all work meets cGMP and regulatory standards. Coordination: Work with QA, QC, Stores, and Maintenance teams for smooth production and equipment upkeep. Team Management: Guide, train, and motivate team members to follow company policies and good manufacturing practices. Safety & EHS: Maintain a safe work environment, ensure PPE usage, report incidents, and follow all EHS rules. Process Improvement: Support productivity enhancement, cost-saving ideas, and new technolog...

Role & responsibilities Manufacturing of Lyophilized Drug Product Aseptic Blending & Filling Injectable Filling Lyophilization BMR Preparation cGMP Practices, Media Preparation, Vial Washing and De-pyrogenation, Validation, Labeling & Packaging, Documentation Preferred candidate profile Aseptic handling Sound knowledge of QMS Sound knowledge of cGMP, GDP

Pfizer Healthcare India Private Limited - Visakhapatnam Hiring Diploma Pharmacy Freshers Job Role - Junior Associates - Manufacturing Eligibility Criteria: Diploma Pharmacy only (2025 Pass out) & Pass Percentage 60% in Academic & No backlogs. Job Description Operate production equipment such as injectable machines, sterile machines, parenteral machines, formulation machines, filling machines, capping machines, compounding machines, washing machines, sealing machines, Visual inspection & packing machines. Monitor and control the production process to ensure quality products are produced within specified parameters. Maintain accurate records of production data and perform routine maintenance t...

A) Execution and Recording: Perform the manufacturing activities as per the BMR and SOP’s. Batch related documents in manufacturing area. Preparation of shift schedule and batch schedule. Readiness related to batch manufacturing. Execution and monitoring of activities in compliance to cGMP. Execution of activities during product change over Checking and timely submission of Batch Manufacturing records to QA. Decontamination and disposable of bio waste. Preparation of MCB/WCB. Automated or manual CIP and SIP of equipment in the manufacturing area. Follow safety norms in the manufacturing area. Self-Inspection of manufacturing area and compliance as per regulatory norms. Operation of SAP S/4 H...

Job Responsibilities: A) Execution and Recording: Perform the manufacturing activities as per the BMR and SOP’s. Batch related documents in manufacturing area. Preparation of shift schedule and batch schedule. Readiness related to batch manufacturing. Execution and monitoring of activities in compliance to cGMP. Execution of activities during product change over Checking and timely submission of Batch Manufacturing records to QA. Decontamination and disposable of bio waste. Preparation of MCB/WCB. Automated or manual CIP and SIP of equipment in the manufacturing area. Follow safety norms in the manufacturing area. Self-Inspection of manufacturing area and compliance as per regulatory norms. ...

Roles and Responsibilities Develop new products by formulating, processing, and developing solid oral dosage forms such as tablets, capsules, granules, etc. Conduct BMR reviews to ensure compliance with GMP guidelines. Collaborate with cross-functional teams for batch manufacturing of OSDs (Oral Solid Dose) products. Ensure knowledge of RMG (Raw Materials Group) management and Batch Manufacturing Record review. Provide support in production activities related to solid oral dosage forms. Identify areas for improvement in production processes, implement changes to increase efficiency and productivity while maintaining quality. Investigate and resolve production issues, including equipment malf...

Charyas is building a modular food-tech factory for functional nutrition bars and gut-friendly snacks. We need a hands-on Factory Lead to run a batch-manufacturing line (roaster mixer extruder cooling packing) with speed, hygiene, and quick changeovers. You will execute daily batches as per formulation sheets/SOPs; operate supervise roaster, mixer, extruder, and flow-wrap machines; plan manpower/materials; ensure GMP, sanitation, and safety; coordinate with RD/QA for trials, first-batch approvals, and scale-ups; maintain batch records, yields, and daily production MIS; and troubleshoot process issues while driving small efficiency improvements and line discipline.

As an Executive / Sr. Executive in the Quality Assurance department with a focus on In-Process Quality Assurance (IPQA), your role will involve: - Performing Line clearance checks according to procedures and conducting various in-process checks, reconciliation verification during different stages of batch manufacturing and packaging. - Preparation and Review of Executed Batch Manufacturing Record and Batch Packing Records. - Taking responsibility for the preparation of Process Validation Protocols, Process Validation Reports, and SOP's. Qualifications required for this position include: - M.Sc in relevant field - B.Pharm or M.Pharm - 2 to 4 years of experience with relevant experience The co...

Experienced professional for API manufacturing operations. 1. Responsible for Handling reactor ,dryers, centrifuge 2. expected to ensure cGMP compliance and BPR review. Reach us at, +91 - 9030508200 (drop your resume) info@pharmacareerhub.net

We are seeking an experienced and dynamic Production Manager to lead the end-to-end lifecycle of pharmaceutical and nutraceutical formulations. The ideal candidate should possess in-depth knowledge and hands-on experience in the manufacturing of Tablets, Capsules, Softgels, Sachets, and Protein Powders. Role & responsibilities A Production Manager in a Pharmaceutical company is responsible for overseeing the formulations, manage all aspects of formulation/ Manufacturing area utilising people, equipment & Materials to meet or exceed the production plan as efficient as possible with minimal wastage of resources 1. Production Planning & Management Develop and implement production schedules to m...

1. Responsible for Operation, cleaning and primary maintenance of negative isolator, Vibro sifter, Bin blenders and all other GEA granulation line equipment. 2. Responsible for recording of activity in logbooks, Batch manufacturing record & complete documentation as required in the manufacturing of product and the cleaning of facilities and equipment, following cGMP s and good documentation practices. 3. To perform all in-process checks and monitoring of all intermediate processes in granulation. 4. To select recipes and set process parameters in Blender HMI & ensure its correctness before blender revolution. 5. Responsible for Issuance, utilization, cleaning, and retrieval of sieves and pro...