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Sun Pharma·Pharma·1 day ago
1 day ago

Jammu Sr_ Officer QC

Jammu, IndiaMid · 2-5 yearsQuality Engineer

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Must-have skills for this role

  • glp
  • gdp
  • process validation
  • analytical method validation

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Apply faster with autofill FREEThe NextRaise extension autofills your application in one click.careers.example.com/applyAutofillingFull namePriya SharmaEmailpriya.sharma@example.comPhone+49 30 1234567LocationBerlGet the extension

What you'll do

  • Analysis of Process validation samples, finished product, Hold time samples and In Process samples.
  • Analysis of Analytical method transfer, Analytical method validation, comparative dissolution profiling and Multimedia dissolution validation activity.
  • On line documentation & Report Preparation.
  • Overall upkeep of respective working bench as well as of the department.
  • To follow the GLP's & GDP's and monitoring of running instrument as per work distribution.
  • Analysis of samples of other sections and calibration of instruments as and when required based on departmental needs.
  • Responsible for participation and input for Out of Specification Investigations, Out of trend & lab Incidents happened in QC department

What they're looking for

  • M.Sc/B.pharma
  • 1-3 Yrs Tenure

Summarised by NextRaise from the employer’s description, which follows in full below.

Full description from employer

 

Job Title:

Analayst - QC

Business Unit:

Global Quality And Compliance

Job Grade

 

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:

  • Analysis of Process validation samples, finished product, Hold time samples and In Process samples.
  • Analysis of Analytical method transfer, Analytical method validation, comparative dissolution profiling and Multimedia dissolution validation activity.
  • On line documentation & Report Preparation.
  • Overall upkeep of respective working bench as well as of the department.
  • To follow the GLP's & GDP's and monitoring of running instrument as per work distribution.
  • Analysis of samples of other sections and calibration of instruments as and when required based on departmental needs.
  • Responsible for participation and input for Out of Specification Investigations, Out of trend & lab Incidents happened in QC department

Travel Estimate

 

Job Requirements

Educational Qualification

 M.Sc/B.pharma

Experience

Tenure:  1-3 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).

           

 

Pharma

Company

Sun PharmaPharma
Jammu, India

Company facts come from this company's own listings. We only show what the postings themselves carry.

Sourced from Sun Pharma's careers site·first seen 19 Sept 2026·last verified 19 Sept 2026·How we source jobs

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