About this role

Executive

Execution, compilation and compliance of qualification and requalification activities of Equipment’s, Utilities and Facility for sterile formulations.
Review of Qualification Protocol and Qualification Report.

Tasks:

HE is authorize to sign (as a doer or reviewer):
Qualification protocol/ Report.
Balance, Weight box and weight calibration report/ certificates and schedule.
Instrument calibration and equipment requalification schedule.
Equipment & Instrument Addition / Deletion.
Calibration related activity.
Regulatory Summary & Query response.
Document issuance and Retrieval.
Non-viable particle count test schedule and test certificates
Filter integrity test schedule and Filter integrity test certificates
Preparation and revision of QE/Validation SOPs.
Preparation and Updation of cGMP documents. E.g. EQMP (Equipment Qualification Master Plan).
Temperature mapping activity.
Handling of any other activities / tasks allotted by department head.
Travel Estimate
Low
Job Requirements
Educational Qualification
Bachelor / Master of Pharmacy

7+ 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).

Executive