Description:
SRG is working with a pharmaceutical company. We are looking for a QA Officer to join the team. A fantastic opportunity to strengthen your skills within a pharmaceutical environment working with experienced team members.
We are seeking a detail-oriented and experienced quality specialist with a background in pharmaceuticals and good manufacturing Practice (GMP).
Responsibilities:
- Maintain and improve QMS performance by ensuring items such as deviations, CAPA and change controls for which you are the owner of are progressed in a compliant and timely manner.
- Ensure products and associated documentation are fit for purpose before release for use or commercial sale.
- Support the maintenance of the site QMS and facilitate reporting of relevant KPIs within department and across site as required.
- Ensure customer or supplier complaints are satisfactorily investigated and communicated.
- Deals with all customer requests and queries within a timely manner in line with company procedures.
- Participate and host internal and external audits inclusive of customer and regulatory audits.
- Author, review, and approve Controlled Documents and QMS items in accordance with procedures.
- Support hosting of regulatory and customer audits.
- Support in the maintenance of Validation activities across all departments.
Requirements:
- Bachelor’s degree (or equivalent) in pharmacy, Life Sciences, or related field.
- Minimum of 1 years’ experience in quality within a pharmaceutical GMP environment.
- Excellent analytical, communication, written and problem-solving skills.
- Ability to work independently and collaboratively in a fast-paced environment.