Accuprec Research Labs Pvt Ltd. is FDCA approved, OECD-GLP, NABL accredited and ISO 9001:2015 certified CRO. Head Quarter of the CRO is located at Ahmedabad and branch offices at Canada and USA. Accuprec provides all type of Pharmaceutical testing solutions to its domestic and MNC clients.
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Research Associate / Sr. Research Associate
Qualification : M.Sc./M.Pharm or equivalent education
Experience : 3-5 years
Job Description : • Analytical method development on various instruments like Particle size/ Zetasizer, Auto-titrator, UV - Visible Spectrophotometer, HPLC/
• UHPIC, ICP - OES/MS, Ion Chromatography.
• Analytical method validation of different methodology
• Dissolution Method Development and validation
• Validation and method development protocol and report preparation.
Research Associate / Sr. Research Associate (Reviewer)
Qualification : M.Sc./M.Pharm or equivalent education
Experience : 5-7 years
Job Description : • Review of analytical data of routine analysis.
• Review of analytical development protocols & report.
• Preparation of routine calculation sheet & validation of calculation sheet.
• To support/guide analytical team in-case of development & validation.
• Report the project status to superior.
Manager (LC, LC-MS)
Qualification : M.Sc./M.Pharm or equivalent education
Experience : 10+ years
Job Description : • Experience of handling team size 5-10 member is mandatory.
• Supervise and lead the team of analytical development, Analytical method validation, technology transfer, forced degradation study, preformulation study, dissolution studies, Extractable and Leachable (E&l) and technical query handling.
• Developed and validate the method of multiple nitrosomine, NDSRI impurities in different molecules on LC-MS/MS.
• Review of analytical development/validation protocols & report.
• Data reliability review of complete document along with accuracy and completeness of computer processed data.
• Report the project status to superior.
Assistant Manager (GC, GC-MS)
Qualification : M.Sc./M.Pharm or equivalent education
Experience : 8-10 years
Job Description : • Experience of handling team size 5-10 member is mandatory.
• Supervise the activities related to analytical Method development and validation.
• Supervise activities related to Extractable and leachable studies.
• Review of analytical development/validation protocols & report.
• Guide the team for Method development for Residual solvents, Nitrosamine and E&L method development and validation.
• Review of raw analytical data of development/validation and routine analysis.
• Report the project status to superior.
Positions Open For Ahmedabad Location. Salary no bar for right candidate.
Interested Candidates send their resumes on mail ID : career@accuprec.in
(Mention your In-Hand Salary, Expected Salary, CTC)
Note : Candidates must have exposure of Pharma regulatory approved organisations (USFDA, MHRA, Eu and other Major regulatory bodies)
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