Sr. Officer - QC

SUN PHARMA; Jammu district; On-site; INR 350,000 - 520,000; Full time

Job summary

SUN PHARMA is hiring a QC Analyst in Jammu to perform analysis of process validation samples, finished products, hold-time and in-process samples, and to ensure precise documentation and reporting. The role requires MSc or B.Pharm and 1–3 years of QC experience, with strong GLP/GDP compliance and instrument monitoring.

Join a dynamic Global Quality and Compliance unit where meticulous testing, data integrity, and cross-functional collaboration drive product quality and regulatory compliance.

Qualifications

• MSc or B.Pharm required
• 1–3 years of relevant QC experience (preferred)
• Familiarity with GLP and GDP practices

Responsibilities

• Analysis of process validation samples, finished product, hold time samples and in-process samples
• Analysis of analytical method transfer and validation, dissolution profiling and multimedia dissolution validation
• On-line documentation and report preparation
• Maintenance of the working bench and departmental upkeep
• Adherence to GLP and GDP guidelines and instrument monitoring as per work distribution
• Calibration and analysis of samples from other sections as required
• Participation in Out of Specification investigations, Out of trend and lab incidents

Education

MSc/B.Pharm

Job description

Job Title

Analayst - QC

Business Unit

Global Quality And Compliance

Location

Jammu

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

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).