Responsibilities · Responsible for Internal Audit as per Schedule. · Responsible for organizing the training all the personnel in the principals of Good manufacturing Practices relevant to the task assigned to them. · Assessing the impact of the training through feedback and appraisals. · Responsible for General Training Programs related to QMS/GMP/SOP. · Responsible for establishment, implementation and maintenance of Quality management system as per cGMP and GLP, WHO and customer requirements. To approve specification, sampling instruction, test methods and other QC procedures. · To ensure online QA checks and compliances to cGMP requirements. · To review, approve and maintain master documents. · Responsible for review and approval of protocol and report of process validation. · To be responsible for implementing a robust system of IPQA, documentation, internal & external audits, quality review meetings etc., and to monitor the same for compliance. · To prepare and review SOPs and to ensure that only current approved SOPs are in use. · To approve the equipment and accessories, AHU and other utility related equipment depending upon it suitability of use before indenting. · To ‘approve’ or ‘reject ‘ all equipment, machinery ,instruments and other electrical and civil engineering materials which are not as per design or of material specification. · To review & approval of protocol and report of equipment qualification. · Responsible to review the records related to change control system as per SOP. · Responsible for review of Market Complaints records. · Responsible for review of Annual Product Quality Review. · Responsible for review of all deviation records as per respective SOP. · Review & evaluate assessment the deviation as per SOP. · To review the Vendor qualification documents Raw material/ Packing material. · Responsible for review of the Vendor audit schedule and Approved Vendor list. · Responsible for review of Batch Production and control record & equipment cleaning record. Job Type: Full-time Pay: Up to ₹65,000.00 per month Work Location: In person
Position: Research Associate (RA) – R&D Preferred Background: API Pharmaceutical Industry Key Responsibilities: Lead and supervise a small team of 2–3 chemists in the R&D laboratory. Plan, execute, and monitor synthetic chemistry experiments related to API development. Maintain accurate and complete laboratory notebooks in compliance with GLP requirements. Ensure safe handling of hazardous chemicals , reagents, and reactions in accordance with safety guidelines. Support and participate in process development and optimization activities. Troubleshoot experimental issues and propose practical solutions. Ensure compliance with internal SOPs, quality standards, and regulatory expectations. Coordinate with senior scientists and cross-functional teams as required. Required Skills & Knowledge: Hands-on experience in API synthesis and pharmaceutical R&D. Good understanding of Good Laboratory Practices (GLP) . Knowledge of hazardous chemical handling , reaction safety, and risk assessment. Basic understanding of process development and scale-up concepts . Strong documentation and data interpretation skills. Ability to lead and mentor junior team members. Qualifications: M.Sc. in Chemistry / Organic Chemistry / Pharmaceutical Chemistry (or equivalent). Relevant industry experience in API R&D is strongly preferred. Job Type: Full-time Pay: ₹20,000.00 - ₹35,000.00 per month Work Location: In person
Position: Research Associate (RA) – R&D Preferred Background: API Pharmaceutical Industry Key Responsibilities: Lead and supervise a small team of 2–3 chemists in the R&D laboratory. Plan, execute, and monitor synthetic chemistry experiments related to API development. Maintain accurate and complete laboratory notebooks in compliance with GLP requirements. Ensure safe handling of hazardous chemicals , reagents, and reactions in accordance with safety guidelines. Support and participate in process development and optimization activities. Troubleshoot experimental issues and propose practical solutions. Ensure compliance with internal SOPs, quality standards, and regulatory expectations. Coordinate with senior scientists and cross-functional teams as required. Required Skills & Knowledge: Hands-on experience in API synthesis and pharmaceutical R&D. Good understanding of Good Laboratory Practices (GLP) . Knowledge of hazardous chemical handling , reaction safety, and risk assessment. Basic understanding of process development and scale-up concepts . Strong documentation and data interpretation skills. Ability to lead and mentor junior team members. Qualifications: M.Sc. in Chemistry / Organic Chemistry / Pharmaceutical Chemistry (or equivalent). Relevant industry experience in API R&D is strongly preferred. Job Type: Full-time Pay: ₹20,000.00 - ₹35,000.00 per month Work Location: In person