Senior Executive - Quality Control

Sun Pharmaceutical Industries, Inc.; Jammu district; On-site; INR 600,000 - 800,000; Full time

Job summary

Sun Pharma in Jammu seeks a Sr. Executive – Quality Control to manage QC documentation, master data, and LIMS activities. The role focuses on maintaining specifications, ATPs, and COAs, while ensuring compliance with pharmacopoeial changes and regulatory expectations.

You'll lead change controls for SOPs and instruments, prepare CQA/COA dossiers, and support commercial and regulatory teams with accurate specifications and data.

Qualifications

• M.Sc/B.Pharm qualification required.
• Familiarity with QC documentation and regulatory submissions is desirable.

Responsibilities

• Prepare QC Master Documents like Specification and ATP in LIMS.
• Import/Export LIMS documents between SUN locations.
• Develop new methods and formulas in LIMS as required.
• LIMS PQ verification and documentation.
• Prepare pharmacopoeial changes reports and update specifications.
• Initiate change control for SOPs, specifications, and STPs in TW software.
• Prepare and revise Quality Control SOP 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 filing.
• Provide Specification/ ATP to Commercial Department.
• Ensure LIMS User IDs creation and deactivation per SOP.
• Initiate change control for installation and qualification of new QC instruments.

Skills

LIMS familiarity

Documentation

Change control

Education

M.Sc/B.pharma

Tools

LIMS

TW software

Job description

Title: Senior Executive - Quality Control

Date: Aug 26, 2026

Location: Jammu - Quality Control

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.

Job Requirements

Educational Qualification

M.Sc/B.pharma

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).