Jubilant Pharma Limited, a globally recognized pharmaceutical company, is hiring Executive – Quality Control and Officer – Quality Assurance professionals for its manufacturing operations. This opportunity is ideal for candidates seeking pharma QC jobs, QA officer jobs in pharmaceutical companies, and GMP compliance roles in India.
Jubilant Pharma operates through its subsidiary Jubilant Generics Limited (JGL) with major R&D centers in Noida and Mysore and manufacturing sites in Mysore, Karnataka and Roorkee, Uttarakhand. Both facilities are approved by global regulatory authorities including USFDA, Japan PMDA, UK MHRA, WHO, and ANVISA, making this a valuable career opportunity for professionals interested in regulated pharmaceutical manufacturing environments.
The company focuses on Active Pharmaceutical Ingredients (API), solid dosage formulations, sterile injectables, and complex molecules targeting therapeutic areas such as CNS and cardiovascular diseases.
Job Roles Available
1. Executive – Quality Control (QC)
The Executive – Quality Control role focuses on stability studies, documentation, and laboratory compliance activities to ensure product quality in accordance with cGMP and GLP standards.
Key Responsibilities
- Qualification and management of stability chambers
- Handling stability samples including loading and withdrawal
- Storage and destruction of samples after testing
- Compilation of stability reports
- Timely analysis of stability samples
- Investigation of deviations, incidents, OOS and OOT results
- Accurate recording of analytical data
- Preparation and review of Standard Operating Procedures (SOPs)
- Conducting self-audits and internal compliance checks
- Ensuring adherence to SOPs, STPs, and GTPs
- Maintaining cGMP and GLP compliance
2. Officer – Quality Assurance (QA)
The Officer – Quality Assurance role focuses on documentation control, batch record management, and regulatory compliance activities.
Key Responsibilities
- Issuance of BMR (Batch Manufacturing Records) and BPR (Batch Packaging Records)
- Issuance of logbooks and documentation formats
- Preparation of master index of SOPs, STPs, specifications, and batch records
- Managing document control activities including issuance, retrieval, and archival
- Archival of executed product-related documents
- Retrieval of obsolete documents before issuing revised versions
- Supporting regulatory submissions and documentation
- Preservation and archival of master records
- Ensuring quick retrieval of stored documents
- Vendor management and preparation of approved vendor lists
Required Qualifications
Candidates applying for Jubilant Pharma QC and QA jobs should typically meet the following requirements:
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, or Life Sciences
- Experience in pharmaceutical quality control or quality assurance
- Knowledge of cGMP, GLP, and regulatory compliance
- Experience in stability studies, documentation, or batch record management
- Strong analytical and documentation skills
Freshers with relevant training or 1–3 years of pharma industry experience may also find suitable opportunities depending on the role.
Why Work at Jubilant Pharma?
Working at Jubilant Pharma provides exposure to globally regulated pharmaceutical manufacturing environments.
Benefits
- Opportunity to work in USFDA-approved manufacturing facilities
- Exposure to API and dosage formulation manufacturing
- Experience with global regulatory compliance
- Career growth in quality assurance and quality control
- Work with experienced R&D and regulatory teams
Jubilant Pharma continues to expand globally with strong revenue growth and a diverse API and formulation portfolio, making it a strong employer for pharma professionals.
How to Apply
Application Link
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