A fully integrated pharmaceutical company engaged in the manufacturing, marketing, and distribution of Active Pharmaceutical Ingredients, pharmaceutical formulations, and medicinal products across the globe.

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At Ipca, our people are core to our success. We aim to build their career and capabilities, and support their individual efforts towards collective growth. Positive and motivated people are the lifeblood of Ipca, and we make sure that our people are duly rewarded, and given ample time to grow individually.

Our performance-oriented culture and dynamic business approach attract top talents in many areas, including R&D, marketing and sales, finance, and administration. This helps us run a team full of young minds as well as industry veterans who work constantly towards improving the lives of millions.

Position: QC Head, API Production

Location: Tarapur Boisar, Maharashtra

Job Description:

  • Overall responsibility of administrative and technical functions of the quality control department
  • Selection & training of new employee

     

  • Selection and Procurement of Laboratory instruments.

     

  • New equipment qualification & approval of IQ/OQ/PQ

     

  • Responsible to monitor the completion of day-to-day analytical work and planning.

     

  • Responsible for the timely release of Raw Materials, Packaging Materials, In-process Results, Intermediates, and Finished Products.

     

  • Responsible for laboratory compliance and develop good laboratory practices.

     

  • Involve in Internal Audits as well as external audits and its compliance.

     

  • Ensure stability Calendar & Stability Analysis Schedule.

     

  • Impart training to personnel (Induction, SOP, GLP, etc.) to improve operational efficiency and for the continual development of QC Personnel and to ensure GLP & safety standards in the laboratory.

  •  

    Reporting deviation and Change control.

     

  • New chemist validation & define job responsibility.

     

  • Approved Protocol for analytical validation & cleaning validation.

     

  • Check and approved Specification, standard test procedure, protocols & analytical worksheet of RM/PM/FG/Stability.

     

  • To ensure quality control specifications and analytical methods are confirming to the latest Pharmacopoeia & customer requirements.

     

  • Deviation, change control & customer complaint are investigated, addressed and closed accordingly with necessary corrective & preventive action.

     

  • Approve Laboratory Trend Data.

     

  • To review and approved analytical reports, COAs.

     

  • To Co-ordinate with outside agencies as and when required.

     

  • To Ensure backup of instruments whenever required taken at the required time

     

  • At time readiness  for any regulatory audit

     

  • Handling deviations, change control, OOS.

     

  • To ensure safety precaution in the laboratory.

     

  • To ensure the implementation of GLP system and CFR part 11 compliance in the laboratory.

Qualification: MS/M.Sc

Experience: 15-24 Years

Salary: Negotiable

Contact Details:

neha.jaybhaye@ipca.com, hrd.mumbai@ipca.com, hrdtech.mumbai@ipca.com

 

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