Executive

Sun Pharmaceutical Industries, Inc.; Panchmahal District; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Sun Pharmaceutical Industries Ltd in Halol-I, Gujarat, India is seeking a Senior Executive to oversee qualification, calibration, and cGMP documentation for sterile formulation facilities. The role demands a strong focus on QA, compliance, and timely delivery of qualification activities.

Candidate should have 7+ years of experience in pharmaceutical qualification, calibration, and related regulatory protocols, with a background in Pharmacy. This is a full-time on-site position at Halol.

Qualifications

• 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.
• Calibration related activities and documentations.

Responsibilities

• Execution, compilation and compliance of qualification and requalification activities for equipment, utilities and facility used in sterile formulations.
• Review of Qualification Protocol and Qualification Report.
• Maintenance of calibration schedules and related records.
• Regulatory documentation and QA sign-off activities.

Education

Bachelor / Master of Pharmacy

Job description

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Company: Sun Pharmaceutical Industries Ltd

Title

Senior Executive

Business Unit

SGO

Job Grade

G11B

Location

Halol-I

Key Responsibilities

• Key Responsibilities:
• 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.

Low

Job Requirements

Educational Qualification

Bachelor / Master of Pharmacy

Experience

7+ years

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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).