For more than 60 years, Ipca has been a crucial healthcare partner in over 120 countries across the 6 continents. IPCA is a fully-integrated pharmaceutical company that manufactures over 350 formulations and 80 APIs for various therapeutic segments. Today, IPCA is one of the worlds largest manufacturers and suppliers of over a dozen APIs. These are produced from scratch at fully-automated manufacturing facilities, approved by the worlds most discerning drug regulatory authorities like UK-MHRA, EDQM-Europe, and WHO-Geneva, among others.

Executive – QMS
Department : API Production
Qualification : BSc / MSc (Chemistry)
Experience : 04-08 Years
Roles & Responsibilities :- Handling of Deviation, OOS/OOT, CAPA & its complaint for respective department. Initiation of departmental Change control proposal, to ensure continues training of employees with cGMP and statutory requirements.

Executive/Chemist
Department : Quality Assurance
Qualification : M.Pharm, B.Pharm, M.Sc, B.Sc
Experience : 02-08 Years
Roles & Responsibilities
Chemist: – Area Clearance and Packing line clearance, Plant round for cGMP compliance. Reviewing completed batch production.
Executive: – Carryout online audit A review and closure of compliance. Handling of Deviation, OOS/OOT, CAPA & its complaint. Initiation of Change control proposal, to ensure continues training of employees with cGMP and statutory requirements. Handling of EDMS software. Initiation of Change control Proposal in Track wise.

Location : Ipca Laboratories Limited, Pologround Indore
Obligatory Note
• Desired candidate should have working experience with WHO, MHRA, USFDA approved Pharmaceutical API plant.
• Turn-up the candidates who is willing to work in Shift Duty.

Interested candidates can share resume on lalit.jangid@ipca.com