Jubilant Pharmova Limited is a leading global pharmaceutical company with a strong presence in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research Development and Manufacturing Organisation (CRDMO), Generics, and Proprietary Novel Drugs businesses. The company operates six world-class manufacturing facilities that cater to regulated markets including the USA, Europe, and other geographies.
Jubilant Pharmova is a part of the Jubilant Bhartia Group, a global conglomerate employing around 42,000 people across multiple sectors, including Pharmaceuticals, Life Science Ingredients, Contract Research & Development Services, and more.
To learn more about Jubilant Pharmova, visit www.jubilantpharmova.com.
Job Responsibilities
As a Senior Executive – Quality Assurance (QA) at Jubilant Pharmova Limited, the selected candidate will be responsible for overseeing quality assurance activities in production blocks and ensuring compliance with regulatory requirements. The key responsibilities include:
- Ensuring quality oversight in production processes, procedures, facility, and training.
- Reviewing and approving batch production records (BPRs) and releasing (or rejecting) API batches.
- Evaluating and closing change control forms, clean room allocation forms, and other related documents before product release.
- Performing visual inspection and line clearance for product changeover activities.
- Ensuring compliance with all Quality Management System (QMS) activities.
- Reviewing training records for production employees.
- Monitoring plant area cleanliness and ensuring compliance with standard operating procedures (SOPs).
- Overseeing equipment calibration, usage logs, and operational efficiency.
- Conducting in-process sampling and ensuring compliance with ALCOA principles for data integrity.
- Handling SAP activities related to production lifecycle management.
- Leading root cause investigations for product failures and customer complaints.
- Coordinating Corrective and Preventive Actions (CAPA) for audit observations and non-conformances.
- Supporting process and cleaning validation activities as per regulatory standards.
Qualifications
The ideal candidate should meet the following educational requirements:
- Postgraduate in Science (M.Sc.)
- Master of Pharmacy (M.Pharm.)
- Bachelor of Engineering (B.E.)
Skills Required
To excel in this role, candidates must possess the following skills:
- Strong knowledge of Quality Assurance (QA) principles in the pharmaceutical industry.
- Expertise in Good Manufacturing Practices (GMP) and regulatory compliance.
- Proficiency in SAP and TrackWise systems for quality management.
- Hands-on experience in handling Quality Management System (QMS) activities.
- Good analytical and problem-solving skills.
- Effective communication and coordination abilities.
- Experience in process and cleaning validation activities.
- Ability to investigate and implement Corrective and Preventive Actions (CAPA).
