Quality Systems and Compliance Manager
Setting the Quality Standard for the site, providing site QA support and management of the Systems & Compliance group.
Responsibilities:
* Ensure that the site quality standards are embedded, measured and sustained in line with Regulatory and Global requirements.
* Preparation and management of the Annual Site Quality Management Plan.
* Providing Overview to site leadership team on the status of the site's quality system through Site Quality Governance Board and Annual Quality Management Review.
* Ensure Global and Local QA Projects and Initiatives are resourced as required.
* Support Quality Culture and Data Integrity on site.
Requirements:
* Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent.
* At least 8 years’ experience working on a manufacturing site (e.g. QA and/or Production) or equivalent experience from external company or other line function. 4 years’ experience leading a team.
* Good working knowledge GMP regulations required within the pharmaceutical industry.
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