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QUALIFICATIONS AND JOB DESCRIPTION
Qualifications
- Background: Preferably graduated from Associate-License Chemistry departments of universities
- Completed military service for male candidates (only applicable to male candidates)
- English: B level (capable to express verbally; understand a conversation; reading and writing)
- Experience: recent graduate or less than 6 months work experience
- Understands the concepts of cGLP and Data Integrity
- Good computer skills, good command of MS Office programs
- Prone to teamwork, analytical thinking, strong communication and relationship management
- Capable to work under pressure, meet deadlines, and work on multiple projects simultaneously
Job Description
- Procurement and management of analytical consumables and external services (outsourcing).
- Assisting in establishment of In-house Infrastructure (Analytical equipment’s Qualifications and preparation of SOP’s).
- Assisting with analytical requirements in finalization of project costings.
- Execute routine Analytical Research activities of drug products (formulation trials and process validation of GMP batches).
- Routinely assess testing monographs and proactively maintain compliance of all activities with current official regulations, pharmacopeias, and SOPs.
- Support analytical methods activities of marketed products (Deficiency letters, methods revamping, etc.).
- Technical assessment & Analysis of drug substances (API) for projects execution.
- Assisting and resolving technical queries raised during Technology transfer activities & regulatory submissions.
- Ensure right first time in all analysis and documentation.
- Preparation of SOPs, ensuring documentation and archive organization.
- Support analytical methods activities of marketed products (Deficiency letters, methods revamping, etc.)
16 Nis 2024;
from:
kariyer.net