QA Validation Records Specialist - 9 Month Contract with potential extension- Fully Onsite
This role will support a strategic project focused on the reconciliation, digitisation, and management of archived validation documentation, including implementation of a new archival system and electronic True Copy process.
Bring energy, knowledge, innovation to carry out the following:
· Review, reconcile, organise, and digitise archived validation documentation.
· Support implementation of a new document archival system for retrospective and prospective records.
· Facilitate conversion of paper records to compliant Electronic True Copy records.
· Assess validation document completeness, criticality, and retention requirements.
· Support archive reorganisation activities in partnership with CQV, Validation, and Document Control.
· Ensure compliance with GMP, GDP, data integrity, and site document management procedures.
· Support compliance reporting and quality system objectives related to documentation management.
What skills you will need:
· BSc in Science, Engineering, Quality, or related discipline (or equivalent relevant experience).
· Experience within a pharmaceutical or other regulated quality environment.
· Knowledge of GMP, GDP, and data integrity requirements.
· Understanding of validation lifecycle documentation and CQV processes.
· Strong document management, organisational, and communication skills.
· Experience with document archival, digitisation, or electronic document management systems is desirable.
· Able to multi-task in fast-paced, dynamic working environment.
