Senior Officer at Sun Pharmaceutical Industries Ltd

Gangtok, Sikkim, India -

Full Time

Start Date

Immediate

Expiry Date

11 Sep, 26

Salary

0.0

Posted On

13 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Good Laboratory Practices, Stability Testing, LIMS, ALCOA++ Principle, Sample Analysis, Calibration, Preventive Maintenance, Stability Protocol Preparation, Quality Control, Laboratory Safety

Industry

Pharmaceutical Manufacturing

Description

Job Title: Senior Officer Business Unit: Global Quality and Compliance Job Grade G12B Location: Ranipool 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: To follow Good Laboratory Practices in the laboratory. To follow the safety precautions (use of nose mask, acid resistant hand gloves, goggles etc.) while handling the strong acids like Sulphuric acid, nitric acid, hydrochloric acid, poisonous chemicals. Ensure all stability chamber are qualified, monitored and suitable for intended use. Prepare stability protocols. Perform sample receipt, incubation and destruction of stability sample. Prepare stability summary reports and stability trend reports. Testing of RM, PM, In-process, finished product, hold time studies and miscellaneous (such as market complaint) samples as per the testing plan. Participation in investigation. To Maintain all the lab instruments, clean externally and internally all the time. To verify the calibration and preventive maintenance status of all instruments before analysis. To make all necessary online entries in instrument usage log, column usage log, working standard log, impurities log as per GLP requirement in line with ALCOA++ principle. To make sample registration, entry of analytical data in LIMS. To maintain online entries of test results in raw data sheet & in LIMS software. To report critical findings to section head and QC head on daily basis. Perform any other task allotted by Quality Control Head Travel Estimate Job Requirements Educational Qualification B.Sc./M.Sc. Experience Tenure: 04 to 06 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).

Responsibilities

Responsible for performing stability testing, sample analysis, and maintaining laboratory instruments according to GLP and ALCOA++ principles. The role involves preparing stability protocols, reporting critical findings, and ensuring all stability chambers are qualified and monitored.