Validation Coordinator
| Dyddiad hysbysebu: | 05 Rhagfyr 2025 |
|---|---|
| Oriau: | Llawn Amser |
| Dyddiad cau: | 26 Rhagfyr 2025 |
| Lleoliad: | Edinburgh, Edinburgh, EH11 2QA |
| Gweithio o bell: | Ar y safle yn unig |
| Cwmni: | SRG |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | BBBH169326_1764932564 |
Crynodeb
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 |
Up to £70p/h |
|
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.
Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.