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

B.Pharm or M.Pharm qualification with atleast 20 years of experience and most recently have 3 years of experience in a multiline commercial manufacturing facility.

Masters Degree in any streams of Biological Sciences; prior work experience with molecular biology techniques gel electrophoresis, Western blotting, Gibson cloning, restriction digestion etc, cell culture. Apart from this, work will also involve routine lab maintenance.

Diploma in Pharmacy from a recognized Institution/ Board, Should be a registered Pharmacist under the Pharmacy Act, 1948.  Desirable, Degree in Pharmacy from a recognized Institution/ University

Diploma in Pharmacy and 3 months training in Pharmacy along with Registration with Central or State Pharmacy Council duly allotted Registration Number. One year experience in a hospital/ Dispensary is essential.

University or college degree in life sciences or related subject, pharmacy, nursing or equivalent relevant degree. Solid knowledge of Clinical Data Management and experience in the Biotech/Pharma/CRO industry.

B.Pharm, M.Pharm and PharmD. This position involves working in US shifts for medical information contact center MICC. Global Inbox management, handling inbound and outbound calls related to medical information, adverse event reports, product quality complaint reports, and medical inquiries.

Pharm D/ MPharm / BDS/ MPH/ MSc (Biostatistics)/ MSc Clinical Research / MSc Nursing. OR MSc Life Science/ BTech Biotechnology with Post graduate Diploma in Clinical Research. To establish a ready network of clinical trial units across the National Cancer Grid to promote multi-centric collaborative

Applications are invited for the following temporary posts in the DBT Research grant under Ramalingaswami Fellow at AIIMS; M.Sc. Life Sciences/ M.Pharm from recognised institute with research experience in cell culture and molecular biology.

Freshers pharma jobs; Walk-in interviews For Freshers M. Pharmacy/B. Pharmacy/ M. Sc Analytical/Microbiology

D.Pharm. / B.Pharm. from a recognized University or Institution. Registered with State Pharmacy Council 

Pharma sales job; dynamic and experienced Key Account Manager to identify key stakeholders and concerned parties that are integral to the success of the sales and account management strategy, to maintain long-term cordial relationships with key customers.

This position will support and manage the regulatory activities associated with the Chemistry, Manufacturing and Controls for New Drug Applications across globe. Regulatory activities focus on filing activities/query responses/post approval changes as suggested across globe.