15 - 20 years

32 - 40 Lacs

Posted:None| Platform: Naukri logo

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Job Type

Full Time

Job Description

Role & responsibilities

  • Minimum 15+ years of experience in the pharmaceutical industry, Preferably in Multi Product API / Intermediate / CDMO or Innovator Products.
  • Strong understanding of USFDA, EU GMP, regulatory compliance, and quality control principles.
  • Prior Experience on Collaboration and Communication with Innovator CDMO organisations.
  • Hands on experience on Digital tools like LIMS, Track wise, SAP HANA, 21 CFR Software Validation etc.
  • Strong customer focus and problem-solving abilities under time bounded efficiency projects. 

Key Responsibilities:

Quality Management System (QMS):

Maintain the QMS, ensuring it aligns with latest industry standards and regulatory requirements. 

GMP Compliance:

Ensure all manufacturing processes and operations adhere to GMP regulations and guidelines.

Audits and Inspections:

Lead and manage internal and external audits and inspections, including those from regulatory agencies. 

Quality Control:

Oversee quality control activities, including analytical testing, method verification & validation, and release of products. 

Team Leadership:

Lead and mentor a team of quality professionals, fostering a culture of quality and continuous improvement. 

Collaboration:

Collaborate with other departments and sites, such as AR&D, DQC, RA, and Supply Chain, to ensure alignment and seamless quality operations. 

Interested candidate please share your updated resume along with

Total Yrs of Experience-  

Where do you work- 

why do you want to change jobs- 

Current Position- 
Current (last) CTC- Expected CTC- Negotiable CTC?-  Notice period- Notice period buyout option?- Current location?- Location change/move- 

on this email : Jyotsna.sable@aartipharmalabs.com

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Aarti Pharmalabs logo
Aarti Pharmalabs

Pharmaceuticals

Mumbai

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