executive

SUN PHARMA; Baksa; On-site; INR 1,200,000 - 1,500,000; Full time

Job summary

Sun Pharma in Baksa is seeking a Sr. Executive for Global Quality and Compliance. You will review QMS documents (Lab Event, OOS/OOT, UPD) and analytical records in the QC lab, ensure cGMP/cGLP compliance, and oversee Lab software like LIMS, Empower and Trackwise. 8–12 years of pharma QA/QC experience is required, with a B.Pharm/M.Pharm/M.Sc. background.

Join us to drive quality, collaborate across teams and support continuous improvement in a fast-paced environment.

Qualifications

• Educational qualification as listed: B.Pharm./M.Pharm./M.Sc.
• 8–12 years of relevant QA/QC experience in pharma.
• Knowledge of CGMP, GLP in QC labs.

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 trail review activity
• Experience for handling Trackwise software

Skills

cGMP compliance

Quality Assurance

Lab QA

Education

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

Tools

LIMS

Empower

Trackwise

Job description

Job Description:

Job Title: Sr. Executive

Business Unit: Global Quality and Compliance

Job Grade: G11B

Location: Baska

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

8-12 yrs

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).

Requirements: