Executive

Sun Pharmaceutical Industries, Inc.

India

On-site

INR 700,000 - 1,100,000

Full time

2 days ago
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Job summary

Sun Pharmaceutical Industries Ltd. is seeking a Sr. Executive in Global Quality and Compliance to oversee QC operations, review QMS events, and ensure adherence to cGMP/cGLP in analytical labs.

The role emphasizes reviewing analytical records, handling LIMS/Empower software, and supporting audits while collaborating across quality teams to maintain compliance and product integrity.

Qualifications

  • Bachelors or higher degree in pharma or life sciences.
  • Experience in QC laboratory and review of analytical records.
  • Knowledge of cGMP/cGLP guidelines in QC labs.

Responsibilities

  • Review of QMS documents (Lab Event, OOS/OOT & UPD investigations).
  • Review analytical records generated in the QC laboratory.
  • Experience in analysis of commercial products (in-process, finished product and stability).
  • Responsible for cGMP, cGLP in QC Lab.
  • Experience with LIMS, Empower and instrument software.
  • Experience with laboratory instrument audit trail reviews.
  • Experience handling Trackwise software.

Skills

QC Lab
QMS Review
GxP Compliance

Education

B.Pharm/M.Pharm/M.Sc.

Tools

LIMS
Empower
Trackwise

Job description

Select how often (in days) to receive an alert: Create Alert

Company: Sun Pharmaceutical Industries Ltd

Job Title:

Sr. Executive

Business Unit:

Global Quality and Compliance

Job Grade
Location:

At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

Are You Ready to Create Your Own Sunshine?

As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

Key responsibilities:
  • Review of QMS (Lab Event, OOS/OOT & UPD investigation) documents.
  • Review of Analytical records generated in the QC laboratory
  • Experience in analysis of commercial product (In process, Finished product

and stability

  • Responsible for cGMP, cGLP in QC Lab.
  • Experience on software like LIMS, Empower and other instrument software
  • Work experience on laboratory instrument Audit trial review activity
  • Experience for handling Trackwise software
Job Requirements
Educational Qualification

B. Pharm. / M. Pharm. / M.Sc.

Experience
Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

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