Home / Job / Granules India Limited – Walk-In Drive for Regulatory Affairs-API on 27th Aug’ 2021

Granules India Limited – Walk-In Drive for Regulatory Affairs-API on 27th Aug’ 2021

Granules India Limited – Walk-In Drive for Regulatory Affairs-API on 27th Aug’ 2021

Walk-In drive – Regulatory Affairs-API @ Granules India Ltd

Walk In drive – REGULATORY AFFAIRS – API

Date: 27 AUG 2021 (FRIDAY)

Time: 9-30AM TO 2PM.

 

Venue: Granules India-Formulation plant-R&D Center- Gagillapur plant-Near Kazipally-Near Gandimaissamma x roads- Medchal road-Hyderabad.

  • Dept: REGULATORY AFFAIRS (APIs)

  • Qualification: M.Sc or M.Pharm

  • Designation: Executives/Sr. Executives

  • Work experience: 3-7 years (Mandatory experience in RA – APIs)

Good Knowledge on:

  • Provide support for Compilation of DMFs and submitting to various regulatory agencies.

  • Preparation of dossiers as per USFDA, EDQM, ASMFs, Heath Canada, WHO and other regulatory agencies dossier requirements.

  • Preparation of responses to queries received from customers and regulatory agencies.

  • Preparation of DMF Amendments/CEP revisions/Other DMF updates to support life cycle management of product.

Placement at Granules – Formulation plant – R&D center-Gandimaissamma x roads-Gagillapur (Near Kazipally), Bowrampet Road-GAGILLAPUR – Hyd.

Kindly carry the below documents with you:

  • Latest copy of CV;

  • All educational certificates;

  • Latest Increment Letter;

  • 3months Pay Slips

Pl mail CVs at: [email protected]

Apply for this position

Allowed Type(s): .pdf, .doc, .docx

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

Check Also

HPLC (Questions & answers)

Q.1- What is the difference between the C8 and C18? Answer: – C8 has 8 …