Senior Officer - QC

Sun Pharmaceutical Industries, Inc.; Dewas; On-site; INR 600,000 - 900,000; Full time

Job summary

Sun Pharmaceutical Industries Ltd in Dewas is seeking a Senior Officer for the Global Quality and Compliance unit. The role focuses on analytical testing of laboratory samples, instrument calibration, and strict cGxP compliance within the QC lab environment.

The candidate should hold M.Sc or B.Pharm with 2–5 years of relevant experience, and will be responsible for maintaining instruments, data records, safety protocols, and continuous process improvements.

Qualifications

• Educational qualification: M.Sc / B.Pharm.
• Experience: 2–5 years in QC lab environment.

Responsibilities

• Analytical Testing: To perform analysis of laboratory samples (Finished APIs, Intermediates, Raw Materials, Recovered Solvent, In-process material, Working Standards) on HPLC/Wet laboratory instruments as per approved Specification, Test procedures and as per customer requirement.
• Laboratory Instruments: To perform and ensure all Wet laboratory instruments are maintained and calibrated as per schedule. To perform daily/weekly calibration of wet laboratory instruments as per schedule. To ensure laboratory instruments (HPLC) are maintained and calibrated as per schedule
• Temperature and Humidity Monitoring QC laboratory and maintain the relevant records.
• Issuance of analytical raw data sheet for relevant analysis.
• Inventory: To maintain inventory of laboratory chemical and documents/spares in HPLC laboratory.
• Sample Handling: Handling and disposal of under test laboratory samples and to ensure that under test laboratory samples are kept as per their recommended conditions and maintain the disposal of under test laboratory samples after completion of analysis.
• Training: To ensure that continuously upgrade the skills through training and technical inputs for knowledge up gradation to drive continuous improvements in laboratory performance.
• Safety: To ensure compliance to cGxP and applicable safety standards in the QC laboratory.
• Verification of general cleaning, destruction of GxP documents and maintenance of related Record. Issuance of analytical raw data sheet and log books for relevant analysis

Skills

HPLC

Analytical Testing

Laboratory Instruments

Quality Control

Education

M.Sc / B.Pharm

Job description

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Company: Sun Pharmaceutical Industries Ltd

Job Title:

Senior Officer

Business Unit:

Global Quality and Compliance

Job Grade

G12B

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

• Analytical Testing: To perform analysis of laboratory samples (Finished API’s, Intermediates, Raw Materials, Recovered Solvent, In-process material, Working Standards) on HPLC/ Wet laboratory instruments as per approved Specification, Test procedures and as per customer requirement.
• Laboratory Instruments: To perform and ensure all Wet laboratory instruments are maintained and calibrated as per schedule. To perform daily/weekly calibration of wet laboratory instruments as per schedule. To ensure laboratory instruments (HPLC) are maintained and calibrated as per schedule
• Temperature and Humidity Monitoring QC laboratory and maintain the relevant records.
• Issuance of analytical raw data sheet for relevant analysis.
• Inventory: To maintain inventory of laboratory chemical and documents/spares in HPLC laboratory.
• Sample Handling: Handling and disposal of under test laboratory samples and to ensure that under test laboratory samples are kept as per their recommended conditions and maintain the disposal of under test laboratory samples after completion of analysis.
• Training: To ensure that continuously upgrade the skills through training and technical inputs for knowledge up gradation to drive continuous improvements in laboratory performance.
• Safety: To ensure compliance to cGxP and applicable safety standards in the QC laboratory.
• Verification of general cleaning, destruction of GxP documents and maintenance of related
• Record. Issuance of analytical raw data sheet and log books for relevant analysis

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).