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Date: Jun 4, 2025
Location: Sun House - Corporate Office
Company: Sun Pharma Laboratories Ltd
Position:
QA Head
Job Title:
QA Head
Job Grade:
(G9 A - Senior Manager 1)
Function:
QA
Sub-function:
Manager’s Job Title:
Skip Level Manager’s Title:
Function Head Title:
Location:
Central or South India (Greenfield Project)
No. of Direct Reports (if any)
3-4
Job Summary
QA Head (Quality Assurance Head) is a leadership role responsible for ensuring the quality and safety of all products and processes, adhering to Good Manufacturing Practices (GMP) and regulatory standards, and overseeing the QA team
Areas of Responsibility
- Expertise in qualification of below process and equipment’s:
- To handle the designing and reviewing of qualification activity of process equipment’s like vial washing, tunnel sterilizer, filling machine, capping machine, Lyophilizer loading and unloading system, Lyophilizer, filtration skid, and isolators, VHP passbox, manufacturing skid, suspension manufacturing skid, CIP SIP skid for manufacturing and filtration equipment’s, dispensing isolators, manufacturing isolators, p H meter, DO meter, integrity tester, Autoclave, Terminal sterilizer, ultrasonication machine, GMP washer, external washing machine, leak test and X ray inspection machine, packing equipment’s etc.
- To handle the designing and reviewing of qualification activity of Utility like Pure steam generation and distribution system, Purified water and WFI generation and distribution system, Nitrogen and compressed air generation and distribution system, AHU, FFM, LAF, area, cold storage etc.
- To review qualification protocol of new equipment like, User requirement specification, Design qualification, Installation qualification, Operational qualification, performance
- qualification and Computer system validation and qualification.
- To ensure compliance to c GMP and documentation for various production activities.
- To review new standard operating procedure for qualification activity and also review SOP of process equipment’s.
- To review schedule for qualification activity, calibration activity, updation of status label of qualification activity etc.
- To review the QMS documents like change control, CAPA, risk assessment, deviation etc.
- To involve during communication with vendor and procurement team on procurement to design parts of new equipment’s along with operation and CFT.
- Ensure proper planning, execution of the qualification activity in accordance with the plan and allocation of man power
- Exposure of regulatory auditors like USFDA, EU, ANVISA, CANADA etc
Medium
Job Scope
Internal Interactions (within the organization)
Check in Internal as well as External both
External Interactions (outside the organization)
Check in Internal as well as External both
Geographical Scope
Financial Accountability (cost/revenue with exclusive authority)
Job Requirements
Educational Qualification
B. Pharmacy, M. Pharmacy .
Specific Certification
Skills
Technical Skills/Competencies (Software packages, experience with specific machines etc.)
Excellent communication skills, strong collaborator, problem solving, interdepartmental coordination, team leadership.
Experience
(15 to 17 Years of experience in relevant field in Pharmaceutical Industry.) Age : 37-42 years
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).
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Seniority level
Seniority level
Director
Employment type
Employment type
Full-time
Job function
Job function
Quality AssuranceIndustries
Pharmaceutical Manufacturing
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