QA/QC Document Controller
We are currently looking for a QA/QC Document Controller to join our analytical services department. The successful candidate will report to the Senior QA/QC Document Controller or Analytical Team Leader on day-to-day issues.
The successful candidate will ideally have a degree which is chemistry or analytical chemistry based.
The ideal candidate will be self-motivated and able to work with minimal supervision. Good interpersonal skills, both verbal and written, are essential for working with both customers and colleagues.
The QA/QC Document Controller will be expected to work within the GMP and safety guidelines set by the company. They will ensure the company Quality Management System (QMS) is maintained and complies with the requirements of Good Manufacturing Practice (GMP) as described in the current EU and ICH guidelines.
Key Qualities and Responsibilities
- Basic understanding of GMP requirements.
- Awareness of the daily requirements of the department.
- Timely review of the following documentation review to a consistently high standard:
- RTID reference standard proformas
- Non-key raw material proformas
- In-process proformas
- Analytical training documents (ATT/AST)
- Level 1 trained in change controls, analytical non-conformance reposts and out of specification procedures.
- Maintain GMP documentation standards at all times.
- Liaise with senior staff within analytical and other departments where required.
- Good time management.
- Awareness of how to be efficient during work hours.
- Awareness of analytical techniques, their applications, and interpretation of results.
- Minimal problem-solving skills, and competency in identifying potential issues.
- Work effectively as part of a team.
- Good positive attitude and self-disciplined.
Benefits:
- Company events
- Cycle to work scheme
- Free parking
- Health & wellbeing programme
- Life insurance
- On-site parking
- Private medical insurance