Description

You will manage validation activities and documentation within GMP manufacturing and warehouse environments.

This role is on-site.

Responsibilities

• Write and review SOPs for security, video, and access control systems.
• Develop SOPs for equipment maintenance and calibration protocols.
• Commission laboratory systems to ensure operational readiness.
• Conduct chamber qualifications and related validation testing.

Required Skills

• 5+ years of experience in the life sciences industry.
• Direct experience working within GMP manufacturing settings.
• Direct experience working within GMP warehouse settings.
• Proven ability to write and review technical SOPs.
• Experience with commissioning lab systems.
• Experience conducting chamber qualifications.

Preferred Skills

• Any Graduate.

Key Skills

Education

Any Graduate