Senior Executive Quality Assurance
- CAPA
- GMP
- Technical Writing
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JOB DESCRIPTION:
Job Description                Â
Followings will be the Core Job Responsibilities of the position holder:
1.   APQR Management
•   Preparation and review of Annual Product Quality Review (APQR) as per defined SOP timelines
•   Compilation of data from:Â
•   Batch manufacturing & packing records
•   Analytical results
•   Deviations, OOS, OOT, CAPA
•   Perform trend analysis and identify:Â
•   Process variability
•   Quality risks
•   Improvement opportunities
•   Ensure completeness, accuracy, and consistency of APR data
•   Provide recommendations and action points based on review
2. Documentation Control
•   Ensure accuracy, completeness, and compliance of all related quality documents
•   Review and control of Supporting documents related to APQR
•   Maintain document lifecycle.Â
•   Ensure document compliance with applicable SOPs and regulatory expectations
3.   Data Integrity & Compliance
•   Ensure data accuracy and traceability in APQR and documentation.
•   Verify consistency of Analytical data, Manufacturing data and QMS records for supporting APQR
•   Ensure compliance with GMP documentation practices (GDP)
4.   Review & Quality Assessment
•   Critically review APQR data for Trends, Exceptions/Deviations and Outliers
•   Highlight discrepancies between data and conclusions
•   Support risk-based decision making
5.   Continuous Improvement (APQR Driven)
•   Identify and recommend process and product improvements
•   Support closure of actions arising from APQR findings
•   Strengthen documentation practices based on audit and review observations
6.   Compliance & Audit Readiness
•   Ensure APQR and documentation are: Audit-ready, Traceable and structured
•   Support internal and external audits related to APQR & Documentation systems
7.   Additional Responsibilities
•   Adhere to SOPs, safety practices, and COBC requirements
•   Perform any other documentation-related assignments as assigned
Key Skills
•   Strong knowledge of:Â
•   APQR / PQR requirements
•   GMP & GDP documentation practices
•   Expertise in:Â
•   Data analysis and trending
•   Technical writing & review
•   Attention to detail and audit readiness mindset
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The base pay for this position is
N/AIn specific locations, the pay range may vary from the range posted.
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JOB FAMILY:
Operations Quality  Â
DIVISION:
EPD Established Pharma    Â
LOCATION:
India > Village Mauza : Baddi  Â
ADDITIONAL LOCATIONS:
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WORK SHIFT:
Standard  Â
TRAVEL:
Not specified  Â
MEDICAL SURVEILLANCE:
Not Applicable  Â
SIGNIFICANT WORK ACTIVITIES:
Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)Â Â Â
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Senior Executive Quality Assurance · wd5:abbott:abbottcareers