Officer-QC (API)

SUN PHARMA; Dewas; On-site; INR 420,000 - 640,000; Full time

Job summary

Sun Pharma in Dewas is seeking an Officer for Global Quality and Compliance. You will perform analytical work on finished product samples, process validation samples, stability samples, RM samples, and cleaning validation samples, ensuring adherence to SAP requests and GMP protocols.

The role requires an M.Sc or B.Pharm and 2–5 years of experience. You will document analytical activity, maintain FP/PV records, assist in OOS/OOT investigations, manage samples, and participate in analytical method

Responsibilities

• Analysis of Finished Product samples, Process Validation samples, Stability samples, RM samples, Cleaning validation samples and Beta-lactam containment monitoring samples as per SAP Request, Protocols and STP's.
• Documentation of analytical activity performed.
• Document analytical data and calculate results.
• Assist in investigation of OOS /OOT /Deviation /Lab Events.
• Management of Finished Product /Process Validation samples as per SOPs.
• Ensure integrity, accuracy and adequacy of the analysis performed.
• Document data accurately and maintain neat/concise/organized FP / PV records.
• Ensure compliance to cGMP requirements and laboratory procedures.
• Preparation of RAPS (Record of analysis) of FP/PV whenever required.
• Participation in analytical method transfer and analytical method Validation activity (Like analysis, Documentation & reporting of results).
• Timely place the indents & procurements of Laboratory chemical & Consumables.
• Recording of results in SAP system.

Education

M.Sc / B.Pharm

Job description

Job Title

Officer

Business Unit

Global Quality and Compliance

Job Grade

G12C

Location

Dewas

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

• Analysis of Finished Product samples /Process Validation samples /Stability samples/ RM. Samples /Cleaning validation samples and Beta-lactam containment monitoring samples as per SAP Request /Process Validation Protocol /Stability Protocol /and Cleaning validation protocol and STP’s.
• Documentation of analytical activity performed.
• Document analytical data and calculate results.
• To assist in investigation of OOS /OOT/Deviation /Lab Events.
• Management of Finished Product /Process Validation samples as per respective SOP’s.
• Ensure integrity, accuracy and adequacy of the analysis performed.
• Document data accurately and maintain neat/concise/organized Finished Product /Process Validation records.
• Ensure compliance to cGMP requirements and laboratory procedures.
• Preparation of RAPS (Record of analysis) of FP/PV Whenever required.
• To participate in analytical method transfer and analytical method Validation activity (Like analysis, Documentation & reporting of results).
• Timely Place the indents & Procurements of Laboratory chemical & Consumables.
• Recording of results in SAP system.

Travel Estimate

Job Requirements

Educational Qualification

M.Sc / B.Pharm

Experience

Tenure : 2-5 years

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).