
Head of Quality, Nottingham
- Nottingham
- Permanent
- Full-time
- Ensuring factory activities in partnership with the site team are fully compliant with regulatory and Reckitt guidelines to minimise risk to consumers, company, and brand name.
- Ensure that any risks to new and existing product developments are identified and communicated prior to introduction to the factories at minimum risk of non-compliance, rejection at time of manufacture or subsequent failure in market.
- Facilitate the identification, communication, and the ongoing removal of identified quality and compliance risks. Communication to Regional Quality director, Site Director and other key function heads as appropriate.
- Management of external regulatory and third-party customer audits received by the factory.
- Provide QA/QC guidance to Co-packers and RB / licences supplied worldwide.
- To provide strong and inspirational leadership to the Site Quality organisation.
- To represent Quality on the Site leadership team, escalating risks and guiding and partnering in solutions.
- To ensure the ongoing compliance of regulated operations, providing expert support and clear, pragmatic advice to the Site.
- Balancing compliance with efficiency; ensuring resources are focussed commensurately with levels of risk.
- To ensure the quality management system is appropriate and compliant and executed efficiently and effectively.
- Broad understanding of manufacturing operations business and quality management systems
- Thorough knowledge of the legal requirements, rules and guidance covering the manufacture of pharmaceutical products in Europe
- Good understanding of Manufacturing, QA and QC testing operations
- Expected to have a proven track record in a manufacturing environment.
- Well-developed leadership skills with a proven track record in driving quality improvements
- Life science degree
- Qualified Person
- Broad understanding of manufacturing operations business and quality management systems
- Thorough knowledge of the legal requirements, rules and guidance covering the manufacture of pharmaceutical & Medical Device products predominantly in Europe and the USA
- Proven track record of leadership in a manufacturing environment.