453 Batch Manufacturing Jobs - Page 2

Operate reactors, centrifuges and dryers, follow SOPs for batch processing, maintain BMR, ensure GMP and safety compliance, handle chemicals, support shift operations, coordinate with QA/EHS, perform cleaning and equipment changeover.

Amneal Pharma Walk-in Drive @ Pharma-SEZ, Matoda, Ahmedabad, (Gujrat) for Production/Packing department (Injectable/ Sterile) on 14th December 2025 (Sunday) We are looking for suitable candidates for injectable/ sterile manufacturing-Packing units for Ahmedabad location. Interview Details: Date: 14th November, 2025 (Sunday), Time: 09:00 AM to 04:00 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 Depar...

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

Prepare BMR, BFR, BPR.QMS Activity (Change Control, CAPA, Incidence).Batch Manufacturing Activity.Batch Filling Activity.Batch Packing Activity.Manpower Handling. Required Candidate profile Education- B.Pharma, M.Pharma & M.Sc. Sterile and Non-Sterile Production Experience

Role & responsibilities Process Validation and Monitoring 1. Monitor process validation batches meticulously, ensuring adherence to established protocols and regulatory requirements. 2. Record observed data accurately and comprehensively, maintaining detailed records of all validation activities. 3. Identify areas for process improvements based on observed data and analysis, proposing solutions to enhance efficiency and product quality. 4. Prepare comprehensive process validation documents, including Batch Manufacturing Records (BMRs), protocols, and reports, ensuring accuracy and completeness. 5. Ensure all process validation activities comply with cGMP guidelines and relevant regulatory st...

Role & responsibilities Candidate must have good knowledge of API Production and Manufacturing process Understanding of Reactor handling and protocol, BPCR/BMR Documentation. Experince in Process handling Batch distillation monitoring and handling shifts as per instruction of shift incharge. Machine handling as per batch requirement Following SoP and ensuring safe batch maufacturing . Preferred candidate profile the desire candidate for API Background to send CV in PFD format Attached to mail witn subject : opening for Chemist / Technician at Ipac Lab - Seloo to tejasvini.kamble.contractor@ipca.com jagpal.dewal@ipca.com

Handling of QMS actives, Change control Deviations market complaints BPR review Process validation review Cleaning validation review APQR preparation Qualification Groups Graduation B.Sc Post Graduation M.Pharma Post Graduation M.Sc Graduation B.Pharma Graduation D Pharmacy

Execute API batch operations as per BMR/BPR and maintain accurate documentation. Operate reactors, centrifuges, filters, dryers and monitor critical parameters. Perform in-process checks to ensure product quality and process compliance. Required Candidate profile Follow cGMP, GDP, SOPs and ensure audit readiness at all times Maintain safety practices, proper PPE usage and support EHS requirements Coordinate with QA, QC, Engineering and Warehouse.

Division Department Sub Department 1 Job Purpose Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift. Key Accountabilities (1/6) Operate the equipment efficiently without error and deviation as per SOP to meet shift targets Perform unit operations as per SOP and unit processes as per batch manufacturing record Optimize the utilization of available resources for achieving production in shift Maintain equipment, facility and block premises as per SOP for audit readiness Key Accountabilities (2/6) Provide suggestions for optimization of processes to manufacture quality product Identify the deficiency in area and errors in documen...

As an Associate Scientist at Syngene International Ltd., your primary focus will be on ensuring safety, compliance, and quality in all work activities within your responsibility area. Your key responsibilities will include: - Monitoring and ensuring adherence to Environment, Occupational Health, Safety, and Sustainability (EHSS) practices for a safe work environment for yourself and your direct reports. - Upholding the highest standards of quality, integrity, and compliance in every work activity. - Completing assigned trainings in a timely manner, following the training procedure, and monitoring compliance for direct reports. - Participating in mandatory trainings related to data integrity,...

1. Manufacturing- Experience Operators Any Diploma / B. Sc with 2 to 12 years of relevant Experience in manufacturing injectables Operate production equipment such as Injectable , Sterile , Parenteral machines, Vial / Ampoule filling , Capping , Compounding , Washing ,Sealing, Terminal sterilization, Stopper process. 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 tasks on equipment as required. Collaborate with other team members to resolve issues and improve overall efficiency. Ensure adherence to Good Manufacturing Practices (GMP) guidelines. Must ha...

Role & responsibilities 1. To supervise production activities such as Manufacturing and packing as allocated by Department Head, as per laid down procedures and systems. 2. To take responsibility of completing daily production targets and documentation thereof. 3. To assist Department Head in preparing SOPs and implementing systems as per current GMP guidelines. 4. To implement discipline, team work and good working atmosphere in the work force. 5. To ensure completion of various cGMP documentation and Batch Manufacturing Records online along with the production activities. 6. To assist Department Head in the training of workmen. 7. To have good relationship and co-ordination with other coll...

Pfizer Healthcare India Private Limited - Visakhapatnam Hiring Diploma Pharmacy / Diploma Mechanical Freshers (2024 & 2025 Batch) Job Role - Junior Associates - Manufacturing Eligibility Criteria: Diploma Pharmacy/ Diploma Mechanical only (2024 & 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 a...

Description/Role: We are seeking a highly skilled and experienced Manufacturing Chemist to join our team in the cosmetics industry. The ideal candidate will have a strong background in cosmetics or pharma KEY DELIVERABLES/ RESPONSIBILITIES Preparing and reviewing of Batch Manufacturing Records and Standard Operating Procedures related to various products applicable to the facility along with R&D Responsible for making batches as per BMR. Responsible for developing, identifying, and modifying new and existing formulations and technologies for improved performance and cost reduction along with R&D All other API manufacturing related work as mandated. Maintaining plant cleaning every day. Use p...

We are seeking a proactive and experienced Manager - Electrical Maintenance to lead efforts in ensuring the reliability, efficiency, and safety of production machinery and electrical systems within our EHV cable manufacturing facility. Key Accountabilities / Responsibilities Oversee electrical maintenance activities for continuous and batch manufacturing processes. Drive improvements in equipment reliability and operational safety. Implement preventive and predictive maintenance strategies. Collaborate with cross-functional teams to minimize downtime and optimize performance. Critical Success Factors - Essential Bachelor s degree in Engineering (Electrical) or equivalent. 8+ years of experie...

Role & responsibilities: Prepare BMR for new products to be processed on the lines. Online BMR, BPR entries to be updated and all formats of relevant SOPs to be completed. Raise material requisition and receive the materials from stores. Preparation of SOPs for the vials and cartridge processing area and ensure training of it for the line operators. To improve the yield of the lines and to reduce the rejections. To prepare the samples as per the customer requirements and complete the entries in BMR and logbooks. To complete the SAP entries for the line activities online. To ensure that the completed batch pallets are transferred to ready to ETO area/ nonsterile FG area and line is ready for ...

Key Responsibilities Handle Product Development & Control (PDC) documentation activities. Maintain batch manufacturing records, specifications, and change controls. Coordinate between QA, QC, and production for documentation updates. Ensure compliance with regulatory and GMP standards. Desired Candidate Profile Experience in PDC/Documentation in pharma manufacturing. Strong knowledge of GMP and documentation practices. Detail-oriented with excellent record-keeping skills.

Technical: cGMP compliance, QA/QMS, Quality Risk Management, Process Validation, Cleaning Validation, APQR, BMR/BPR preparation and review, Packaging material/specification management, Dossier/NDA preparation, Change Control and Deviation Management, Technology transfer, Internal auditing, Documentation control and data integrity (ALCOA+). Soft: Attention to detail, strong documentation and communication skills, cross-functional collaboration, problem-solving, compliance mindset. Domain: Pharmaceutical manufacturing and regulatory inspection support. Quality Risk Management; Batch Manufacturing Record (BMR) preparation; Process Validation; Packaging Material Specification preparation; Annual...

Position: Production Chemist Location: Vapi Experience: 1 - 2 Years Industries: Pharma API Responsibilities: Oversee safe discharge and treatment of effluents. Prepare and maintain batch manufacturing records and other Operational documentation. Conduct quality control tests to ensure product consistency and regulatory compliance. Develop and optimize chemical processes for efficient ... Production Chemist Vapi - Apply JobItUs ATS Qualification: B.Sc - Chemistry; B.Tech/B.E. - Chemical; Diploma - Chemical Position: Production Chemist Experience: 1 - 2 Years Industries: Pharma API Responsibilities: Oversee safe discharge and treatment of effluents. Prepare and maintain batch manufacturing rec...

Roles and Responsibility Manage and oversee the production process to ensure efficient and safe operations. Conduct regular quality checks to maintain high standards of products. Collaborate with cross-functional teams to optimize production processes and improve productivity. Develop and implement new methods and procedures to enhance production efficiency. Ensure compliance with safety protocols and regulations. Analyze data and reports to identify areas for improvement and implement changes. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directl...

Roles and Responsibilities Handling of QAMS, DMS activities Prepare SOP, BMR, ECR and all related docs. as per CGMP To maintain & review all document like change control, INcident with compliance report Involvement in the investigation & review of Incident, Change Control, CAPA, MFR, BMR etc. in QAMS /DMS Handling of manufacturing investigations as part of OOS/OOT/Market Complaint etc.

As a Shift Chemist at the Pharma Manufacturing department, your primary responsibility is to ensure the achievement of the desired production yield of pharmaceutical APIs. This involves ensuring that all production activities in the shift comply with cGMP, cGLP, EHS requirements, and specified operating procedures. Key Responsibilities: - Properly take over shift operations following defined procedures - Follow the Gowning Procedure before entering the pharma area - Indent raw materials from stores and update balance in Material Reconciliation Record - Collect Intermediate material and ensure availability of Utilities before charging the batch - Verify and charge raw material quantities, exe...

Job Description Relevant Experience : Should have experience of Production for Formulation Plant of Oral Solids (Tablets, granules, powder) & Allied in PHARMACEUTICAL COMPANY / FACTORY. FDA Approval in Tablet Section Pharma Formulation plant would be preferred. 1. Batch Manufacturing Manufacture production batches as per Batch Manufacturing Record (BMR) and Batch Production Record (BPR). 2. BMR/BPR Documentation Complete the online BMR and BPR as per the respective activities. 3. Coordination with QA Coordinate with the Quality Assurance (QA) department for the issuance of monthly formats. 4. Manufacturing Parameters Review Review parameters during manufacturing stages such as compression, f...

To issue the Batch Manufacturing Record, Equipment cleaning record, Logbooks, Analytical Report for raw material, finish product and packing material. Assistance in preparation of SOP of various departments/ preparation of draft SOPs. Required Candidate profile QMS Experience in API (Pharmaceutical) whatsapp CV on 9724346949

Interview for Production & QC For MNC Chemical Co in Dahej 05-12,Friday 1. Production : BSC / Diploma : 3 to 10: 4.5 LPA 2. QC : BSC / MSC Che : 2 to 6 Years : 4.5 LPA Apply : sdpbharuch@gamil.com Subject : Production/QC Dahej Required Candidate profile Time : 9:00 to 3:00 Walk-In Venue: SDP HR Solution 6th Floor, 611, Golden Square, Beside DMART, Near ABC Circle, Bholav, Bharuch