June 2024

M.Sc./ M.Pharm or equivalent education at Accuprec Research Labs Pvt Ltd. is FDCA approved, OECD-GLP, NABL accredited and ISO 9001 2015 certified CRO.

M.Sc, M.Pharm; Experience must include analysis of Raw Material, In-Process, finished goods, Stability Testing and Stability sample handling Tablets / Capsules. Handling of HPLC, dissolution and other sophisticated instruments.

M.Sc/ M.Tech./ M.Pharm IPR from a recognized University. The incumbent should have sound knowledge of Patent Act, 1970 and should possess five years post qualification experience in dealing with issues like filling of Patent, Design, Copy Right & Trade Marks. Master degree in biotechnology/Molecular & Cell Biology/ Pharmacology/ Microbiology/ Biochemistry

Masters Degree in Pharmaceutical Sciences / Chemical Sciences/ Forensic Sciences from a recognized university or equivalent institute. and Scholars who are selected through National Eligibility Tests-CSIR-UGC NET

Pharmaceutical Regulatory Affairs and Management ; Ph.D in relevant discipline and MPharm Pharmaceutical Regulatory Affairs/ Quality Assurance

FR&D Department / Technology Transfer / Project Management - Injectables; Evaluation of impurity profiles of drug substance and drug product. Hands on experience with development of Injectable solutions, lyophilized drug products and other complex Injectables.

M.Sc /B.Pharma; Exposure in HPLC, GC, Wet Analysis, LIMS, Microbiology, Stability areas. Exposure in Exposure in IPQA, QMS , Validations, SOP Preparations, Protocols, ERP works, MRP, MFR, MI, PORM, cGMP guidelines.

OE Lead would be a key resource working closely with the Sun Global Operations leadership to identify, analyse and resolve manufacturing issues and align supply to business demand

University or college degree in the life sciences or pharmacy, nursing or equivalent relevant degree. Proficient knowledge of clinical coding process. Experienced in using MEDDRA and WHO-DD coding dictionaries