CY Partners have an exciting new opportunity as a QA Manager in Pharma R&D at a Global Pharmaceutical Company. You will be a part of the Infrastructure and Validation function and perform the quality assurance activities and quality oversight of the Validation and GMP facilities management activities performed within Pharma R&D across the UK sites.
The role is an initial 6 month contract and is fully on site.
In this role your responsibilities will include
- Providing review and approval of validation lifecycle documents from a variety of QMS within the company. Provide meaningful comments to ensure compliance with regulatory expectations/requirements.
- Provide quality oversight of internal business groups and external services partners inclusive of the following quality processes:
- Change control
- Deviation investigation inclusive of CAPA.
- May support project work as a QA representative, quality program or team activities.
- Provide advice and consultancy to project teams
Role Requirements
- Proven working experience in biopharma/pharmaceutical Industry related to Quality Assurance Job scope.
- Experience of validation of analytical systems, cold chain storage, secondary manufacturing equipment, utilities and infrastructure. Computer validation if possible for networked systems and corporate facing applications.
- Experience with key Quality activities (i.e. Deviations Change Controls)
- Excellent organisational skills
- Strong interpersonal skills.
- Strong written and verbal communication skills.