Quality Assurance Specialist (Phamaceutical)

Key Responsibilities:

Process Validation: Ensuring that the manufacturing processes are validated to meet the required quality standards.

Documentation: Maintaining accurate and complete documentation of the technology transfer process.

Compliance: Ensuring that the transferred processes comply with Good Manufacturing Practices (GMP) and other regulatory requirements.

Collaboration: Working closely with R&D, manufacturing, and other departments to ensure a smooth and successful technology transfer.

Training: Ensuring that manufacturing personnel are adequately trained on the new technologies and processes.

Audits: Conducting audits to ensure that the transferred processes are operating as intended and in compliance with regulations.

Skills and Experience:

• Bachelor's degree in Engineering, Quality Assurance, Life Sciences, or a related field.
• Strong knowledge of GMP and regulatory requirements.
• Experience in pharmaceutical quality assurance.
• Experience in process validation.
• Excellent communication and collaboration skills.