5+

Expertise of Finish goods testing, Stability, RM Testing, Analytical Method Validation, Dissolution, HPLC, PMQC, Microbiologist and knowledge of handle other sophisticated instruments Like GC, XRD, ICPMS, LCMS.

M.Pharm, B.Pharm, M.Sc ; Exposure of Leak Test Skid operations Exposure of Ampho/ Bupivacaine Autoclave Operation Lyo Operation Filling/ Vial washing Batch Manufacturing

BACHELOR OF PHARMACY, BACHELOR OF SCIENCE ( B.Sc Degree ), MASTER OF PHARMACY; Validate clinical trial data to ensure consistency, integrity and accuracy based on project specific guidelines. Responsible & Accountable for the assigned study conduct activities, in clinical trials from TCS.

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