185 Pharmaceutical Production Jobs

Responsibilities: * Pharmaceutical Manufacturing tablet, liquid and syrup. Process validation, BMR and requisite making. Supervision and testing for in process validation. * Oversee production planning, execution & quality control.

Role & responsibilities Min 2-6 years experience working with Pharma API Plant. Responsibility includes adherence to SOPs/to meet production targets, maintain GMP & Safety practices. Able to handle and analyze process problems in manufacturing. Sound knowledge of operations of centrifuge/reactors etc.

shall be responsible for maintaining and improving all QMS activity, GMP and GLP across the company Handling QMS activities like change control, validations, stability, qualifications, APQR and Risk assessment etc Label artwork review and management Required Candidate profile Assisting HOD in customer complaint analysis and preparation of customer complaint report. Investigation of incidents, deviations, OOS and ensure corrective actions in place.

Ensure timely execution of production plans maintain quality standards, optimize resources and solvent recovery ensure GMP safety compliance lead process improvements foster team development interdepartmental collaboration and timely issue reporting

Role & responsibilities The Production Manager will be the technical and operational lead for our chemical manufacturing facility, responsible for ensuring safe, high-quality, and cost-efficient production. This role involves managing the entire production lifecycle, optimizing processes, and ensuring strict compliance with all safety and regulatory standards. Production Planning: Develop and execute production schedules to meet volume, quality, and deadline targets. Safety & Compliance (SHE): Enforce strict adherence to all EHS (Environment, Health, Safety) and regulatory protocols (e.g., OSHA, local chemical handling laws). Quality Management: Implement and monitor quality control processe...

Supervise and manage shift production in excipients/food plant. Ensure GMP compliance, quality output, manpower utilization, safety, and process efficiency. Coordinate with QA & maintenance to meet production targets. apply : hr@celluloseankit.com

Interview for OSD Pharma Formulation Plant in Bharuch on Company Payroll Date : 09-11, Sunday Operator & Officer Can Apply Exp: 1 to 13 Yrs CTC: As per Interview Work Location: Dahej Apply: sdpbharuch@gmail.com Subject: OSD Bharuch Free Job Required Candidate profile Vacancies Officer - 30 Senior Officer - 16 Executive - 4 Machine Operator (All production & Packing) - 30 Experience in OSD Plant in Must Share with Your Colleagues & Seniors Free Job Placement

Responsibilities: To handle shift production in plant To handle the troubleshooting in shift operations Maintain batch production records, log book and register for proper documentation Responsible for adherence to SOPs for all plant operations Execute the daily planned and scheduled work for completing the production plan Required Skills Logical thinking. Organizing. Good in communication. Required Qualification: - Diploma/B.E/B.Tech/B.Sc/M.Sc - Chemistry

2 yrs exp as Head of Engg. Must have faced USFDA Audits/EU/MHRA Audits in previous companies. Should have Process Equipment & Utilities Experience in Oral Solid Dosage & Injectable Plants (Major OSD / Minor - Injectable experience will do).

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....

- Manage the development, performance and maintenance of the manufacturing production. - Manage Production & Procurement Planning based on Estimation. - Responsibility to adhere to budgets and plan to maximize profitability. Required Candidate profile - Good understanding of manufacturing production management, requirements and dynamics. - Excellent analytical, interpersonal, organizational and communication skills.

Job description: Role: Production Shift in-charge B.sc /M. Sc/Diploma chemical 5-10 yrs working experience in API and intermediate plant having a good GMP knowledge 50- 75 k / PM Employment Type: Full Time, Permanent Role Category: Production & Manufacturing - Other Education: UG: B.Pharma in Any Specialization, Diploma in Chemical, B.Sc in Any Specialization PG: PG Diploma in Chemical, M.Pharma in Any Specialization, MS/M.Sc(Science) in Any Specialization

1. Overall maintenance of Plant (Civil, Electrical and Mechanical) 2. Increase efficiency by planning, delegation and governance 3. Coordination with vendor, contractor or third party to deliver optimal output within budget and timeline 4. Coordination with various departments within company for smoothen the day to day operation 5. Reduce the incidence of costly breakdowns and develop strategies to improve overall reliability and safety of plant, personnel and production processes. 6. Ensure continuous running of equipment and machinery 7. Ensure that all machinery need to be well conditioned and well maintained at all the time 8. Participate in various audit (WHO, PICS etc.) 9. Supervision ...

API Production Chemist experience (BSc Chemistry): Operates reactors, centrifuges, dryers executes batches per BMR/BPR; ensures GMP/cGMP, safety & documentation monitors yield, process parameters supports process improvement & shift operations Perks and benefits Canteen & Transportation Facilitys

Data Search & Analysis on the drug discovery and development Creating technology reports Kindly provide minimum two references with resume Required Candidate profile Keen interest in drug discovery, API Good Knowledge of organic chemistry Good Communication Skills

Data Search & Analysis on the drug discovery and development Creating technology reports Kindly provide minimum two references with resume Required Candidate profile Keen interest in drug discovery, API Good Knowledge of organic chemistry Good Communication Skills

Responsibilities: * Collaborate with R&D on new product launches * Ensure compliance with BMR & Reqs, API production standards * Oversee pharmaceutical production processes * Manage team performance and development

Key Responsibilities: 1. Production Operations: Execute and supervise daily Softgel manufacturing operations including gelatin mass preparation, encapsulation, drying, and inspection . Ensure all activities are carried out as per BMR, SOP, and cGMP requirements. Coordinate with QA and QC for in-process checks and line clearance. Maintain process parameters (temperature, humidity, viscosity, machine settings, etc.) within specified limits. 2. Documentation & Compliance: Prepare and maintain Batch Manufacturing Records (BMR) , logbooks, and equipment usage logs. Ensure timely completion and accuracy of documentation as per Good Documentation Practices (GDP) . Adhere to data integrity and regul...

As a Process Engineer at Shriyata Lifetech Private Limited, you will play a crucial role in designing and optimizing cutting-edge processes in the Pharmaceutical or Biopharmaceutical industry. Your responsibilities will involve: - Designing, developing, and optimizing processes for pharmaceutical and biopharmaceutical production. - Collaborating with R&D, manufacturing, and quality teams to ensure process efficiency and regulatory compliance. - Troubleshooting process-related challenges and implementing effective solutions. - Preparing and reviewing process documentation, SOPs, and technical reports. - Supporting scale-up activities and technology transfer from lab to commercial production. ...

Allocation of the work to work force, perform the critical checks & its documents, line clearance at all stages of packing. implement good manufacturing practices in the department. production & packing of tablet/capsule & granules as per cGMP.

Design and conduct experiments to create and refine new drug compounds. Research new materials and compounds for potential medicinal use. Analyze how substances interact with biological systems and human tissue.

Responsibilities: * Oversee production processes at our Ahmedabad facility * Ensure compliance with BMR & Req standards * Collaborate with R&D on API development and implementation

Trainee - Operator: Educational Qualification - Diploma in Engineering (Mechanical/Electrical/Electron ics) Experience - 0 - 3 years experience of operating pharmaceutical manufacturing machines in Ointment & Liquid section Job Responsibilities - To operate machines related to manufacturing andpacking activities of Semi Solid Dosage(Ointment), ExternalPreparations & Liquid oral. To adhere with cGMP & SOP Compliance in the department and ensure safety & quality ofproduct during manufacturing & packing operation To achieve desired production targets, control of wastage and yield improvement during process operations. To do online in process checks and donecessary entries in BPR at regular inte...

Role & responsibilities 1. Shall responsible for Production planning in consultation with the Plant Incharge. 2. Shall maintain compliance as per SOP, Quality Policy and compliance in relation to regulatory bodies legislation within Production department. 3. Shall responsible to ensure appropriate labelling system in Production department as per SOP. 4. Shall responsible to ensure that approved manufacturing procedure available for all product manufactured in the plant and shall ensure that all manufacturing operations are performed as per the approved manufacturing process. 5. Shall responsible to check Batch Production and Control Record. 6. Shall involve in the Market Complaint investigat...

A reputed pharmaceutical liquid formulation unit requires an experienced Quality Assurance Chemist, audit-ready and well-versed in GC operations. The candidate should be capable of handling QA documentation and compliance effectively.