Home / Job / Ipca Laboratories Ltd – Openings for AMV (Analytical Method Validation)

Ipca Laboratories Ltd – Openings for AMV (Analytical Method Validation)

Ipca Laboratories Ltd – Openings for AMV (Analytical Method Validation)

Ipca Laboratories - Wikipedia

Company : Ipca Laboratories Ltd (Formulation Unit)

  • Location : Pithampur SEZ (MP)

  • Department : AMV (Analytical Method Validation)

  • Qualification : B Pharm / MSc / M Pharm

  • Experience : 3 to 7 (Not for Fresher)

  • Openings: 10

Job Responsibilities:

  • Should have good knowledge about sophisticated instrument like Waters HPLC, Perkin GC system with Empower 3 software.

  • Should have knowledge about Analytical method validation, Analytical method verification and Analytical method transfer as per various guidelines (like ICH, USP etc) and cGLP requirement.

  • Aware about compliance of Laboratory with ALCOA, system SOPs, specification and method of analysis.

  • To prepare protocols and worksheet for analytical method validation, analytical method transfer and analytical method verification activities.

  • To perform calibration of AMV instruments and equipment as per procedure in AMV Lab and have to review their documents.

  • To perform cleaning validation and have to handle activities of QMS e.g. Incidents, Deviations etc.


Shubham Joshi,

Ipca Laboratories Ltd.

Pithampur SEZ

[email protected]

T : 07292667008

Interested Candidate Share your CV on [email protected],

Apply for this position

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About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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