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GMP Validation Professional

2 months ago

Scotland, United Kingdom SRG Full time

About the Role:

SRG is seeking a highly skilled Validation Specialist/Technician to join our team. As a key member of our operations, you will be responsible for ensuring the highest standards of quality and compliance in our pharmaceutical manufacturing processes.

Key Responsibilities:

  • Develop and implement validation protocols for equipment and processes in a GMP environment
  • Conduct hands-on validation activities, including protocol writing, execution, and report writing
  • Coordinate and manage sample collection and testing
  • Collaborate with cross-functional teams to ensure seamless integration of validation activities
  • Stay up-to-date with industry regulations and best practices, and implement changes as necessary

Requirements:

  • Qualification or significant practical experience in a related scientific discipline
  • Knowledge of validation principles within a GMP environment
  • Experience with autoclaves, ovens, HVAC, freeze dryers, equipment washers, and/or process/computer validation
  • Proven track record of working in a pharmaceutical environment

What We Offer:

SRG is a dynamic and growing company that values innovation, collaboration, and excellence. As a Validation Specialist/Technician with SRG, you will have the opportunity to work with a talented team of professionals, develop your skills and expertise, and contribute to the success of our organization.