5+

M.Pharm, B.Pharm, M.Sc, B.Sc, ITI, Diploma; Candidates required for manufacturing Tablet/ Capsule - Granulation, Compression, Coating, Inspection. Responsible to plan for the manufacturing of batches in coordination with PPMC.

B. Pharm / M.Pharm; Supervision of Granulation Activity. Candidate should have exposure of FBD, RMG, Octagonal Blender, Bin Blender, Multi Mill, Cone Mill, Shifter etc. Production QMS, Quality Management System, Handling of QMS activities like Deviation, Incident, Investigation, CCP, Protocol Preparation, Risk Assessment etc.

B.Pharm / B.Sc / M.Sc; To perform IPQA Packing/Manufacturing, BMR,BPR review, Line Clearance, Review of Batch Production and Control Record BPCR,Review of Logbooks

Graduate / Postgraduate in Pharmacy. Develop stability study designs for new product development and sustaining product projects. Make sound technical recommendations regarding stability study designs for new product development and sustaining product projects that are more routine than not.

Sr. Specialist Regulatory Affairs will independently, with minimum supervision, initiate and prepare the regulatory submissions, interact with Business Units Regulatory affairs teams and interact with regulatory agencies/health authorities to obtain and maintain product approvals with a focus on India, Sri Lanka and other SWA Countries, as per the country specific regulations.

experience in Pharmaceutical / Biotech / Clinical Research industry with Clinical Operations. candidate for the Manager clinical operations role who can provide local strategic planning and operational delivery of clinical studies through all phases of study management preparation, study start-up, conduct, close-out, and manages local vendors

B.Pharma/M.Pharma; Site Transfer of approved products from one facility to another facility. Evaluation and Selection of Optimal batch sizes for scaling up using scientific scale up techniques as guidance based on manufacturing process and equipment capacities for Registration batches and Launch commercial production.

Bachelor or Masters in Life Sciences, Healthcare, Business Administration, Engineering or Information Technology. Handle Product Technical Complaints and Field Alerts for medical devices, pharmaceutical products, biologics, and combination products, ensuring compliance with regulatory standards.

M.Pharm; Design and conduct experiments to characterize the physical, chemical, and biological properties of drug formulations. Collaborate with cross-functional teams, including R&D, Quality Assurance, and Regulatory Affairs, to ensure successful project outcomes.