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 the Quality Operations team on the release of products.
As Qualified Person, you will:
1. Carry out the review of batch manufacturing documentation relating to oral solid dose production.
2. Prepare documentation for QP release in a timely manner.
3. Investigate and close out deviations while working in close cooperation with other departments.
4. Identify and implement corrective and preventative actions.
5. Participate in, and lead, relevant Quality Risk Management Assessments.
6. Participate in internal and external audits as required.
7. Be involved in the continuous improvement of Quality systems.
Education & Experience:
1. Eligible to act as Qualified Person.
2. Degree in Chemistry/Analytical Science/Pharmaceutical Science or Forensic Science.
3. Strong IT skills.
4. Strong attention to detail.
This role operates under a hybrid working policy, 3 days on-site and 2 days from home.
This role would be the perfect opportunity for someone who is QP eligible and hoping to gain experience on a manufacturing license. For more information, reach out at c.croker@masonalexander.ie.
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