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.
Job Title
Validation Co-ordinator
Contract Type
Fixed-Term Contract (6 Months)
Location
Edinburgh
Salary
£40,000 per annum (pro-rata)
Hours
37.5 hours per week (Monday to Friday)
Start Date
Immediate
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