Job Description

• Review quality management systems and approve the documents like SOPs, Protocols, SMF, VMP, QSM, Drawings, batch record, etc and manufacturing IPQA activity. • Hands-on experience with all conventional and sophisticated analytical instruments. • Meet qualification and validation activities process and handle deviations, Incidences, change controls, OOS and market complaints. • Review and update of Site Master File, Validation Master Plan, Quality Manual, Calibration Master Plan and batch record and analysis data and batch release. • Implementation of training programs and current Good Manufacturing Practices and approve the layouts. • Conduct, review and Implementation of internal audits. Suggest the CAPA and close the non-compliance report observed during internal audits and review the compliance of both internal and external audits. • Review, approve and implementation of risk assessment programs.

Requirements

- Academic degree in Biology, Chemistry, Pharmacy or similar field - At least 4 years of relevant experience working with establishment of Device/Pharmaceutical manufacturing and/or manufacturing Pharmaceutical products - The ideal candidate will need an open mindset who can work independently and as a team player with a strong focus on results, to succeed in this role - Good communication skills with the ability to establish good relationship with local and global team - Fluent in English, both written and oral - Ideal Age Range: 28- 38

Employment Type

  • Full Time

Details

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