Cadila Pharmaceuticals Hiring Technology Transfer Department
- About Cadila Pharmaceuticals
- Open Position
- Key Responsibilities
- Preferred Skill Set
- Courses Covered Under M.Pharm:
- Why Choose Cadila Pharmaceuticals?
- Job Summary Table
M.Pharm Jobs in Technology Transfer – Cadila Pharmaceuticals Hiring at Dholka Plant
Apply now for M.Pharm jobs at Cadila Pharmaceuticals in the Technology Transfer department. 2–6 years of experience required. Location: Dholka, Gujarat.
Career Opportunity in Technology Transfer for M.Pharm Graduates at Cadila Pharmaceuticals – Dholka, Gujarat
Cadila Pharmaceuticals, a pioneer in the Indian pharmaceutical industry, is inviting applications from qualified M.Pharm professionals for positions in its Technology Transfer department. With a strong legacy of innovation and quality, Cadila is looking to strengthen its technical workforce at its Dholka manufacturing facility in Gujarat.
This role is ideal for candidates with 2 to 6 years of experience in technology transfer, scale-up, validation, and regulatory compliance in pharmaceutical manufacturing.
About Cadila Pharmaceuticals
Cadila Pharmaceuticals is one of India’s largest privately held pharmaceutical companies, known for its excellence in R&D, regulatory standards, and global presence. The company continues to make significant contributions to healthcare through innovation and affordable solutions.
Open Position
Department: Technology Transfer
- Designation: Officer / Executive (based on experience)
- Qualification: M. Pharm (Pharmaceutics/Industrial Pharmacy preferred)
- Experience Required: 2 to 6 Years
- Work Location: Dholka Plant, Gujarat
Key Responsibilities
Technology Transfer Activities:
- Facilitate transfer of products from R&D to the commercial manufacturing facility.
- Oversee QMS-related processes, receiving activities, and documentation handling.
Scale-Up and Troubleshooting:
- Execute scale-up and exhibit batches, ensuring equipment capacity and regulatory alignment.
- Collaborate with the production team to resolve process-related challenges.
Documentation and Compliance:
- Draft/review GMP documents such as:
- SOPs
- Batch Manufacturing Records
- Sampling Protocols
- Hold Time and Stability Study Reports
- Process Validation Protocols
- Provide support in QMS activities such as:
- Change controls
- Deviation and OOS investigations
- CAPA implementation
Regulatory and cGMP Adherence:
- Maintain compliance with current Good Manufacturing Practices (cGMP) and global regulatory requirements.
Preferred Skill Set
- In-depth knowledge of GMP, technology transfer protocols, and process validation
- Strong command of documentation practices and regulatory expectations
- Excellent collaboration and communication abilities
- Problem-solving and analytical thinking
Courses Covered Under M.Pharm:
- Pharmaceutics
- Industrial Pharmacy
- Pharmaceutical Quality Assurance
- Pharmaceutical Regulatory Affairs
- Drug Development and Scale-Up
- Process Validation Techniques
Why Choose Cadila Pharmaceuticals?
- Opportunity to work in a technologically advanced manufacturing setup
- Exposure to complex pharmaceutical processes and regulatory landscapes
- Career growth within one of India’s most respected pharma companies
- Be a part of a team driving innovation in generic and specialty medicines
Job Summary Table
| Company Name | Cadila Pharmaceuticals |
|---|---|
| Current Vacancies | Technology Transfer Department |
| Required Education | M. Pharm |
| Experience Required | 2 to 6 Years |
| Location | Dholka Plant – Gujarat |
To apply for this job email your details to drashti.chaudhari@cadilapharma.com
