Sr. Officer

SUN PHARMA; Jammu district; On-site; INR 700,000 - 1,000,000; Full time

Job summary

SUN PHARMA is seeking an OSD QA Documentation Supervisor in Jammu to oversee documentation control, ensure traceability, and support QA processes across the Global Quality and Compliance unit.

The role involves managing BMR/BPR issuance, training assignments, and data compilation for process validation and annual product reviews, while coordinating with SAP and EDMS/BRMS systems.

Qualifications

• B.Pharma or MSc required for the role.
• 4–5 years of QA documentation experience preferred.
• Familiarity with GMP/QA documentation systems and audits.

Responsibilities

• Issue BMR/BPR and related pages to user departments.
• Manage and control QA documents and records.
• Maintain logbooks, formats, and control samples; ensure timely updates.

Skills

Documentation control

QA processes

SAP

Change control

Education

B.Pharma / M.Sc

Tools

Trackwise

EDMS

BRMS

SAP

Job description

Job Title

OSD QA Documentation Supervisor

Business Unit

Global Quality And Compliance

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

• Issuance of BMR/BPR
• Issuance of extra pages and formats to user departments.
• Handling and controlling of all documents and records.
• Retrieval of old QA related documents and records.
• Assigning of training no. for training and other sheet to user department.
• Management of control sample room.
• Update and maintain signature logbook.
• Issuance and preparation of Hold time validation report.
• Issuance, controlling and retrieval of monthly formats and logbooks.
• Preparation of annual product review.
• Monitoring of environment in control sample room and walk-in cold chamber.
• Trackwise, EDMS, EDAMS, BRMS and SAP related activity.
• Responsible to initiate Change Control, Unplanned Deviation, CAPA and Temporary Change Control
• Responsible for review of Process validation protocol
• Responsible for preparation and data compilation of Process Validation Report
• Responsible for Qualification of Plant Equipment (Protocol Preparation, Review and Execution
• Responsible for preparation of Vendor Risk Assessment report and Approved Vendor List.

Job Requirements

Educational Qualification

B.Pharma/M.SC.

Experience

Tenure : 4-5 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).