Job Description: Validation Co-ordinator

Job Summary

SRG are seeking a proactive and detail-oriented Validation Co-ordinator to join our Validation department for our client that specializes in the development and manufacture of active pharmaceutical ingredients for the pharmaceutical and biotechnology industries on a 6-month fixed-term basis. This role is critical in ensuring that validation activities across production and quality functions are executed effectively and in compliance with regulatory standards.

Key Responsibilities

• Liaise closely with Manufacturing, Development, and Quality departments to support validation activities.
• Develop strategies for individual validation studies in consultation with cross-functional teams, considering past experiences, company policies, and product-specific needs.
• Prepare and maintain Validation Master Plans.
• Coordinate validation plans in alignment with production schedules.
• Collate historical data and pre-validation manufacturing information to support protocol development.
• Author qualification and validation protocols and reports for both process and cleaning validation.
• Assist in equipment and software qualification, including execution and approval of non-critical deviations.
• Conduct periodic qualification reviews.
• Perform risk assessments related to validation activities, including change control evaluations.

Ideal Candidate Profile

• Experience in validation within pharmaceutical or manufacturing environments.
• Strong understanding of GMP and regulatory compliance.
• Excellent communication and coordination skills.
• Ability to work collaboratively across departments.
• Analytical mindset with attention to detail.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.