Syngene Executive Vacancy 2021 – Pharma & Chemistry Apply Online
Chemistry and Pharma job opening 2021. Pharma jobs Syngene Pharma.Syngene Job. Chemistry Candidates with MSc are encouraged to apply online at Syngene for vacancies that are available. Syngene is hiring Chemistry candidates. Interested and eligible candidates may apply online. Check out all the details on Rasayanika.com
Job Title: 9-I (Executive)
Job Location: Bangalore.
Department: Quality Control Common.
Job Description:
Responsible for performing the physicochemical and instrumental analysis (HPLC, Dissolution, UPLC, GC, KF, pXRD, particle size, etc.) and investigations
(Drug Substance, Drug Product, Intermediate and Excipient)
- 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.
- Ensure and comply with EHSS and safety policies laid down by the organization.
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.
Educational Qualification:
M. Pharmacy or M.Sc. (Analytical Chemistry/Organic Chemistry)
Technical/Functional Skills:
- 0 to 3 years of working experience in Stability or 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 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:
0 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.
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