Medley Pharmaceuticals Hiring Production Officer (API)/Assistant Manager Production/QA Officer apply now

Medley Pharmaceuticals Hiring Production Officer (API)/Assistant Manager Production/QA Officer apply now

Vacancy details:
  • Post Name:  Production Officer (API)/Assistant Manager Production/QA Officer
  • Qualification: B.Pharma – Pharmacy, B.Sc – Any Specialization PG:M.Pharma – Pharmacy, MS/M.Sc(Science) – Any Specialization
  • Experienced:7 – 12 Years
  • Location: Tarapur
  • Salary :NA
  • Openings :NA
  • Recruiter Name:Jyoti
 Job Description: We have requirement for the post of Production Officer (API)/Assistant Manager Production/QA Officer in Medley Pharmaceuticals Ltd !
1-Responsible for monthly production planning, Execution & monitoring.
2-Responsible for all daily operation and production of commercial API.
3-To train all shift supervisor and operators about unit operations, safety and SOP.
4-Technology transfer coordinator jointly with R&D & QA.
5-Handle production QMS documents like Change control, Deviations, OOS.
6-Responsible for regulatory audits & customer’s audit CAPA & Implementation of CAPAs.
7-Overall Responsible for Production related SOP, review and implementation at site.
8-Conducting training for new recruited production chemist in terms of cGMP/ GDP aspects and Safety aspects.
  1. To maintain and control an overall quality management system documentation.
  2. Responsible for the preparation planning, coordination and execution of QA training programme. Assessment of other departments training
  3. Issuance of batch number, batch manufacturing record, Register, SOP’s, format, protocols, Analytical protocols to departments
  4. To review the Analytical records, Batch manufacturing record and batch packing record
  5. Preparation of QA-SOP’s, Validation protocol aPQR, summary reports based on the Analytical results and Batch documents data.
  6. To coordinate for the validation activities with other department for successful completion
  7. Submit customer questionnaire along with declarations, management of free samples.
  8. Maintaining vendor approval process
  9. Daily assessment of site to ensure GMP compliance level of site through round.
  10. Management of regulatory and customer audit at site
  11. Management of Deviation, Incident. Change control, OOS, Recall, Market complaint, Investigation, CAPA, Risk assessment etc
  12. Interpretation of sales order and overall management of dispatch
  13. Reviewing stability data and sharing inference with management.
  14. Providing data to Regulatory patent or any other authorities
Selection ProcessThe selection will be on the basis of Interview.


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