447 Batch Manufacturing Jobs

Role & responsibilities 1. Ensure compliances of Good Manufacturing Practices in Kilo Lab. 2. Prepare the area / section for batch production as per QA guidelines. 3. Supervise equipment operation in assigned production area and maintain critical process parameters as mentioned in Batch Manufacturing Record (BMR). 4. Ensure all solvents & raw materials required for the production activity are available in advance. Verify that correct Raw Material has been issued. 5. Fill all the required data in Batch Manufacturing Record (BMR). 6. Check critical steps of process and maintain records. 7. Promptly report any abnormal observation/activity, deviation, in process QC results to Shift-In Charge. 8...

Preferred candidate profile Diploma in pharmacy/mechanical/electrical with minimum 1 year experience in OSD production. Recruiter Mohaneswara https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities Operate Fluid Bed Equipment and Spheroniser as per SOP, including cleaning and line clearance activities to ensure readiness for production. Strict adherence to safety, health and environment. Carry out Manufacturing activities by following and monitoring standard operating procedure (SOP) and current Good Manufacturing Practice (cGMP). To ensure effective implementation of RFT and Data integrity policy. Maintenance, upkeep of the department, premises, and equipment. To maintain disci...

Washing Area 1. To carry out the sterilization related activities in Bung Processor, H.P.H.V steam sterilizer. 2. To carry out the operation and cleaning of vial washing machine & Depyrogenating tunnel as per SOP. 3. To ensure that preventive maintenance of the machine which done by maintenance department as per schedule. 4. To assure the proper maintenance of change parts of Bung Processor, H.P.H.V steam sterilizer, Depyrogenating tunnel & vial washing machine 5. To carry out the all filter integrity & maintain related documents. 6. To maintain BMR & Equipment logbooks and general logbooks. Manufacturing (Aseptic Area) 1. To carry out the sterile Area related activities in Filling & Sealing...

Sections: Tablet, Capsule, External Preparations & Oral Liquids We are inviting applications for the position of Approved Manufacturing Chemist to join our growing pharmaceutical production team. This role is a vital part of our manufacturing operations, ensuring that every batch of product is produced with the highest standards of quality, safety, and compliance . The Approved Manufacturing Chemist will be responsible for overseeing production processes in Tablet, Capsule, External, and Oral Liquid sections . The ideal candidate will not only have the necessary Drug Control Department approval but also a passion for maintaining excellence in pharmaceutical manufacture Key Responsibilities S...

Employment Type : - Full Time Salary Range : - No bar for the right candidate Experience : - 20+Yrs. Reporting to : - Promoter - Technical Level : - Senior Leadership Note : - This position will lead the operations of 5 different production sites of Aether with a total reporting of 600 employees. Job Objective To take full command of end-to-end plant operations in a high-performance specialty chemicals environment. This role demands a technically competent, results-driven operations leader with proven experience in batch manufacturing, solvent recovery systems, compliance-heavy processes, and multi-step reaction management. The Head of Operations will be accountable for achieving production ...

Ensure compliance with cGMP, WHO, and regulatory guidelines. Handle batch planning, manpower management, and documentation. Monitor aseptic practices, machine operations, and production output.

Title: Production Manager (Aerosol & Nasal Spray) Business Unit: SGO Job Grade G10 Location : Halol-II 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.” JOB DESCRIPTION- 1. Preparation and sign...

Job Title: Oracle EBS Manufacturing Functional Consultant Location: Bengaluru or Pune (Hybrid) Engagement: 6 Months Contract to Hire IMPORTANT PLEASE READ BEFORE APPLYING Candidates must be comfortable with a contract-to-hire engagement. Only apply if available to join ASAP. Willingness to work in a hybrid model (3 days onsite, 2 days remote). Job Description: We are seeking an Oracle EBS Manufacturing Functional Consultant to support and enhance Oracle E-Business Suite Manufacturing processes. The role focuses on managing end-to-end manufacturing operations and working closely with business stakeholders. Key Responsibilities: Act as a functional expert for Oracle EBS Manufacturing covering ...

Role & responsibilities We are looking for candidates having hands on experience in the API manufacturing sector to handle API Production activities like intermediate , Clean room , Shift incharge role . Solvent recovery experienced candidates can also apply. Preferred candidate profile : Only Male Candidates Junior officer - Diploma in Chemical Engineering ,BSC ,MSc in Chemistry Officer -Diploma in Chemical Engineering ,BSC ,MSc in Chemistry, BTech . Executive - BSC ,MSc in Chemistry ,B.Tech in Chemical Engineering .

Role & responsibilities: Your job responsibilities are listed below for your understanding and acceptance. In case of any system up-gradation in future, you will be simultaneously re-trained to understand the new implementation. 1. Responsible Manufacturing of Oral Liquid and for Production planning as per order or availability of material. 2. Responsible for Preparation of BMR for new product. 3. Responsible for verifying the filled BMR and yield reconciliation of each stage. 4. Responsible for preparation of Standard Operating Procedure (SOPs). 5. Responsible for Preparation MFR for new product development. 6. Responsible for coordinating with Eng. department for Preventive maintenance. 7....

Ensure the batch charging as per production plan.. Verification of Raw material input in to the batches. Review of BPR & ECR. To perform qualification /validation activities as per protocol To ensure GMP activities as per norms in the plant.

1. Daily Production Activities Operate and monitor production equipment under supervision. Ensure smooth running of production processes and support machine start-up/shutdown. Record production data accurately in logbooks. Assist in batch preparation and material handling. 2. Compliance & Safety Follow GMP/GLP guidelines and other industry regulations. Adhere to safety standards, including PPE usage and hazardous material handling. 3. Quality & Process Monitoring Conduct in-process checks (temperature, pressure, weight, volume). Identify and report deviations, abnormalities, or equipment malfunctions. Ensure proper storage and labeling of raw materials, intermediates, and finished goods. 4. ...

Hands-on with reactor operations, filtration, drying, and crystallization. Experienced in batch processing, in-process monitoring, and scale-up activities.Strong understanding of Good Manufacturing Practices (GMP) Required Candidate profile - Education: B.Sc./M.Sc. in Chemistry/Pharmaceutical Sciences - Experience: 1–2+ years in API Production Perks and benefits GMP GLP plant| Growth| Safety| Compliance| Perks

Job Title: Manager Production (Aseptic) Business Unit: Sun Global Operations Job Grade G11A/G10 Location : Baska 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.” Key responsibilities: Aseptic area & Aseptic manufa...

Sr. Officer - QALL: Work Location - Baddi, Baroda & Navsari Ensure GMP/GLP compliance at Contract Manufacturing sitesand third party sites and provide registration documents and required support for registration from site. Ensure availability of current valid masterdocuments like raw material /packing material /finished product specificationsbatch manufacturing record /batch packing record at site and retrieval ofobsolete documents. To check and find non compliances at Contract Manufacturing /Third Party location and ensure corrective and preventive action. To execute, ensure and monitor processvalidation / Technology Transfer activities, Unit Operation, QMS Compliance atsite and arrange for...

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Preferred candidate profile Diploma in pharmacy/mechanical/electrical with minimum 1 year experience in pellets production. Recruiter Mohaneswara https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities Operate Fluid Bed Equipment and Spheroniser as per SOP, including cleaning and line clearance activities to ensure readiness for production. Strict adherence to safety, health and environment. Carry out Manufacturing activities by following and monitoring standard operating procedure (SOP) and current Good Manufacturing Practice (cGMP). To ensure effective implementation of RFT and Data integrity policy. Maintenance, upkeep of the department, premises, and equipment. To maintain d...

As a Manufacturing Chemist, you will be responsible for overseeing and managing the formulation and production processes of cosmetic products. Your main focus will be to ensure that all manufacturing activities comply with regulatory standards, product specifications, and quality norms, while maintaining efficiency and safety. **Key Responsibilities:** - Supervise and execute batch manufacturing of cosmetic products such as creams, lotions, talc, lip balm, etc. as per SOPs and BMR. - Ensure accurate weighing, mixing, heating, cooling, and filling of raw materials and ingredients as per approved formulations. - Maintain hygiene and GMP standards in the manufacturing area. - Conduct in-process...

Execute API batch operations, monitor process parameters, operate reactors/centrifuges/dryers, ensure cGMP & safety compliance, maintain documentation, coordinate with QC/QA/EHS, handle shifts, support audits, and ensure housekeeping & 5S.

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