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Title:  Senior Officer

Date:  Apr 8, 2026
Location:  Sikkim I - Plant
Company:  Sun Pharma Laboratories Ltd

Job Title:

Senior Officer QA - Training IRA

Business Unit:

Global Quality And Compliance

Job Grade

G12B

Location :

Gangtok

 

 

 

 

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:

  • Site EDMS coordinator.
  • To update active user list of EDMS/BRMS/EDAMS users of the site.
  • To initiate UAM for EDMS account activation/deactivation/modification of site.
  • To prepare, review distribution, retrieval of controlled SOPs & Forms.
  • To maintain master copy of forms for Business continuity plan.
  • To implement GQS and GSOP at site & coordinate with other department.
  • To update of global documents tracker.
  • To initiate and evaluation of change control request for revision/ implementation of site SOP/global documents.
  • LMS (Training) coordinator of department.
  • Prepare curriculum in LMS of revised / new implemented SOP.
  • Update MTNM of QA department.
  • To impart training as per Integrated training calendar.
  • To coordinate quality related training conducted by global CQPT team at site i.e. IACP, Auditor certification etc.
  • To review training file of QA employees.
  • To conduct induction training of new Joinees.
  • Maintain signature log of all employees.
  • To update site master file.
  • Management of document archival in Enterprises Document Archival Management System (EDAMS) at site.
  • To track QA site risk assessment on regular basis.
  • To review and release of artwork.
  • To prepare the draft label of existing product for license application and coordinate with FDD and PDD.
  • To prepare COPP and apply for approval.
  • To renew NDPS license application as per frequency.
  • To review of Qualification protocols and reports.
  • To update status of Pharmacopoeial evaluation.
  • To prepare investigation report of IPA sample investigation report.
  • To prepare investigation report of NSQ sample. 

Travel Estimate

 

Job Requirements

Educational Qualification

M.Sc / B.Pharm / B.sc

Experience

Tenure:  4 to 6 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).

 

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