Cadila Pharmaceuticals Hiring Technology Transfer Department

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