Job Description: We are looking for a Site Quality Leader/QP to partner our Skelmersdale Medical & Healthcare products (MHRA) and Secondary Manufacturing licensed site to support our strategic priorities and business needs ensuring effective site compliance. The role will focus onsupporting an agile and flexible on-site QA (Quality Assurance) organisation, you will apply superior change management expertise in the areas of culture, skills, expectations and incentives tomanage this high performing site. Within your assignment you will manage a team of three, engage and collaborate with the organisation and not be afraid to challenge to push through improvement. The role will be challenging and significant from the first day and an outstanding amount of learning and experience will strengthen your personal and professional development. Job Responsibilities: Have full oversight and development for the Quality Systems programme, full investigation and reporting of any quality deviations, attend all Quality Council site meetings and responsible for quality scorecard and management reviews Build collaborative business relationship with internal and external partners Constantly drive to deliver high standards of GMP/GDP (Good Manufacturing Practices and Good Distribution practices) and ensure compliance can be demonstrated and records are maintained Have knowledge of products traded under the licences and access to pharmaceutical knowledge where required and assuring correct licensing is in place Review batch manufacturing documentation to ensure compliance with EU Good Manufacturing Practice (GMP) Certify Medicinal products for use in the EU and outside the EU and control release of other products stored at the site Provide advice and guidance to staff regarding pharma regulations with the support of the Registration Authorities (RA) team and provide input on any proposed updates or variations Job Requirements: Essential: Able to provide evidence of eligibility of Qualified Person (QP) (UK) Proven experience acting as a QP in pharmaceutical/biological manufacturing businesses Good working knowledge of current requirements for Good Manufacturing Practices and Good Distribution Practices Strong experience in delivering against operational and strategic business priorities and handling QA activities on a large scale Attitude of continuously striving for excellence, and ability to take calculated risk to achieve superior results Excellent collaboration skills, together with ability to influence others Ability to work independently with tight timelines and multiple priorities in a fast-paced environment Job Details: Company: P&G Vacancy Type: Full Time Job Location: Liverpool, GB Application Deadline: N/A Apply Here careers-trivia.net
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