Cadila Pharmaceuticals, one of India’s leading pharmaceutical manufacturers, is inviting applications from experienced Quality Control (QC) and Quality Assurance (QA) professionals for its Dholka formulation facility. This is an excellent opportunity for candidates with formulation industry experience to advance their careers in regulated manufacturing, analytical testing, and compliance-driven environments.
The company is looking for skilled professionals in microbiology, analytical instrumentation, and IPQA functions who can ensure product quality aligned with cGMP, GLP, and regulatory standards.
📍 Job Location
Dholka, Gujarat
💼 Open Positions
Quality Control (QC) Department
Designation: Officer to Executive
Sections:
- Microbiologist
- HPLC Analyst
- GC Analyst
- GLP (Good Laboratory Practices)
- FP (Finished Product Testing)
Qualification: B.Sc / M.Sc / B.Pharm
Experience: 2 to 7 Years (Formulation Industry Mandatory)
Quality Assurance (QA) Department
Designation: Officer to Senior Executive
Sections:
- IPQA (In-Process Quality Assurance)
- Lab QA
Qualification: B.Pharm / M.Pharm
Experience: 2 to 7 Years (Formulation Industry Mandatory)
🔬 Key Responsibilities
Quality Control Roles
- Perform analytical testing of raw materials, in-process samples, and finished products.
- Operate and calibrate instruments such as HPLC, GC, and microbiological testing systems.
- Ensure compliance with GLP, cGMP, and regulatory guidelines.
- Conduct method execution, documentation, and laboratory investigations.
- Maintain analytical records, logbooks, and stability data.
Quality Assurance Roles
- Monitor manufacturing processes through IPQA activities.
- Ensure batch documentation review and compliance with SOPs.
- Handle deviation management, CAPA, and change control.
- Support audits, validations, and regulatory inspections.
- Maintain quality systems aligned with global regulatory requirements.
🎓 Eligibility Criteria
- Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm (as per role).
- Experience: 2–7 years in pharmaceutical formulation manufacturing.
- Strong understanding of:
- cGMP & GLP practices
- Regulatory documentation
- Analytical instrumentation
- Quality systems & compliance
- Prior experience in formulation plants is mandatory.
💰 Salary (Estimated)
₹4.5 LPA – ₹8.5 LPA (Based on experience, role, and technical expertise)
🌟 Why Join Cadila Pharmaceuticals?
- Opportunity to work with a reputed Indian pharma leader.
- Exposure to regulated manufacturing and global quality standards.
- Career growth in QA/QC specialization domains.
- Hands-on experience with advanced analytical technologies.
- Stable, compliance-driven pharmaceutical environment.
📩 How to Apply
Interested candidates can share their updated CV to:
📧 jimit.sharma@cadilapharma.com
