Syngene Executive Quality Control – Chemistry & Pharma Job
Syngene Pharma.Syngene Job. Pharma Candidates with MSc are encouraged to apply online at Syngene for vacancies that are available. Syngene is hiring M Pharma candidates. Interested and eligible candidates may apply online. Check out all the details
Job Title: Executive Quality Control Common.
Job Location: Bangalore.
Department: Quality Control Common.
Educational Qualification: M. Pharmacy or M.Sc. (Analytical Chemistry/Organic Chemistry)
Technical/Functional Skills:
- 2.5 to 3 years of working experience in Stability and Quality control.
- The candidate should have experience in the analysis of drug substances and drug products.
- Good analytical skill and shall perform analysis right the first time.
- Hand on experience of HPLC, GC, KF coulometer, KF titrator, Dissolution tester, and IR. (experience in PXRD, DSC, Particle size analysis, LCMS is preferred.
- Experience in Chromeleon software, LIMS, Trackwise will be an added advantage.
- Good understanding of GMP, GDP, and data integrity principles.
- Quick learner and early change adaptor.
- Experience in regulatory audits is a must.
Experience:
2.5 to 3 years of working experience in Stability and Quality control. (Drug substances and drug products)
Behavioral Skills:
- Effective time Management.
- Reading Comprehension
- Communicating effectively: verbally and writing
- Team player.
Job Description:
- Responsible for performing the physicochemical and instrumental analysis and investigations (Drug substance, Drug Product, Intermediate and Excipient) for stability testing lab.
- Responsible for performing analytical method validation and analytical method transfer.
- Deliver results ‘Right First Time’ and within the established windows.
- Participation in internal, client and regulatory audits.
- Compliance with quality systems in laboratory.
- Ensure and comply with GMP, GDP, Data Integrity EHS policies laid down by the organization.
- Flexibility to work in any project/team as per the requirement.
Preparation of documents like stability summary reports, stability protocols, SOP. - Responsible for audit readiness.
- Performance of instrument calibration, qualification whenever required.
Key Responsibilities:
- First pass analysis of stability samples i.e. drug substances and drug products.
Ontime escalation of laboratory issues. - Initiation of QMS records on time
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