We are delighted to be working with a well established pharmaceutical company, with an excellent reputation as a great place to work, on a Qualified Person permanent position.
This role will report to the Quality Operations Manager and will work alongside Quality Operations team on the release of products.
Responsibilities:
- Carrying out the review of batch manufacturing documentation relating to oral solid dose production.
- Preparing documentation for QP release in a timely manner.
- Investigating and close out of deviations while working in close co-operation with other departments.
- Identifying and implementing corrective and preventative actions.
- Participate in, and lead, relevant Quality Risk Management Assessments.
- Participating in internal and external audits as required.
- Being involved in the continuous improvement of Quality systems.
Requirements:
- Eligible to act as Qualified Person.
- Degree in Chemistry/Analytical Science/ Pharmaceutical Science or Forensic Science.
- Strong IT skills.
- Strong attention to detail.
