Job Reference: J5633991
Updated On: 02/11/2020
Status: Open to Applications
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Role OverviewI'm currently recruiting a Senior Quality Specialist to join a leading Drug Development and Manufacturing business based in the Newport area. As the Senior Quality Specialist you will be responsible for the following:
Key Duties and ResponsibilitiesYour duties as the Senior Quality Specialist will be varied, however the key duties and responsibilities are as follows:
1.Support strategic clients with projects from the development phase through to commercial supply.
2.Perform Batch Reviews to support QP certification.
3.Review and approve Technical documentation, ensuring compliance to GMP.
4.Support investigations into deviations, out of specification results and change requests to GMP compliance.
Role RequirementsTo be successful in your application to this exciting opportunity as the Senior Quality Specialist we are looking to identify the following on your profile and past history:
1.Relevant degree in within a Scientific discipline
2. Proven industry experience within the pharmaceutical sector
3. Working knowledge and practical experience of Quality within a pharmaceutical manufacturing business.
Key Words: Quality, Pharmaceutical, GMP, Batch review, GXP. Quality Assurance
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