Senior Executive - Quality Control

SUN PHARMA; Jammu district; On-site; INR 900,000 - 1,500,000; Full time

Job summary

Sun Pharma in Jammu is seeking a Sr. Executive – QC to manage QC master documents, LIMS-based specifications and ATPs, and support regulatory filings. You will oversee new method and formula preparation, PQ verification, and change control activities across QC operations.

The role requires 8–10 years of pharma QA/QC experience, MSc or BPharm, and hands-on knowledge of LIMS, SOPs, and CPP/COA processes. Join a team committed to quality and compliance in a dynamic environment.

Qualifications

• M.Sc or B.Pharm degree required.
• 8-10 years of pharma QC/QA experience.
• Hands-on knowledge of LIMS, SOPs and regulatory filings.

Responsibilities

• Prepare QC Master Documents like Specification and ATP in LIMS for materials.
• Import/Export of LIMS documents between SUN locations.
• Prepare new methods and formula documentation in LIMS.
• LIMS verification (PQ) and documentation.
• Prepare pharmacopoeial changes reports and update specifications.
• Initiate change control for SOPs, specifications and STPs in TW software.
• Prepare and revise QC SOPs per GQS/GSOP.
• Index preparation and updation of Specification.
• Prepare FP dispatch COA and regulatory submission COA.
• Provide Specification/ATP for dossier filing and regulatory submission.
• Provide Specification/ATP to Commercial Department.
• Ensure LIMS user ID creation and deactivation per SOP.
• Initiate change control for installation and qualification of new QC instruments.

Skills

LIMS

Documentation

Quality control

SOPs

COA

Education

M.Sc

B.Pharm

Tools

TW software

Job description

Job Title

Sr. Executive – QC

Business Unit

Global Quality And Compliance

Job Grade

G11B

Location :

Jammu

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 will 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

• To prepare the QC Master Documents like Specification and ATP [For Raw Materials, Working Standard, Finish, Stability and Packing Materials etc.] in LIMS.
• To Import/Export of LIMS documents from and to SUN locations.
• New Methods preparation and Formula preparation in LIMS as per Requirements.
• LIMS Software Verification [PQ] & Documentation.
• Preparation of Pharmacopoeial changes report based on Verification of Pharmacopoeial Methods raw data. Responsible for updation of Specification as per Pharmacopoeial changes Report.
• To initiate the change control for the revision and preparation of SOPs, Specifications, Standard Test Procedures etc. in TW software.
• To prepare and revise Quality Control SOP as per GQS & GSOP.
• Index preparation and updation of Specification.
• To prepare FP dispatch COA and regulatory submission COA .
• To provide Specification/ ATP for dossier filing and re-filing to regulatory.
• To provide Specification/ ATP to Commercial Department.
• To ensure LIMS User ID creation and deactivation of QA and QC department as per SOP.
• Responsible for initiation of change control for installation and Qualification of new received QC Instruments.

Educational Qualification

M.Sc/B.pharma

Experience

Tenure : 8-10 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).