Social network you want to login/join with:Team Horizon - Head of QualityTeam Horizon is seeking a Head of Quality for our client's manufacturing facility in the Midlands. In this role, you will oversee the Quality Assurance and Quality Control Teams, support the implementation, maintenance, and continual improvement of the company QMS, and undertake the role of QP named on the relevant MIA(s).Why you should apply:Opportunity to work with a diversified portfolio of products across multiple therapeutic areas, with strengths in analgesics and anti-infectives.Excellent chance to utilise QP eligibility and leadership experience in a Head of QA position overseeing Quality Assurance and Quality Control teams.Highly competitive salary & benefits on offer.What you will be doing:Ensure an appropriate, compliant QMS is in place to ensure site compliance, including regulator inspections, and optimal throughput of products.Perform QP certification of products for release to market, aligning with business requirements and release schedules.Manage site quality operations and batch certification activities, ensuring compliance and timely batch release.Review (or delegate review of) batch documentation related to manufacture and testing, and certify products for release in accordance with GMP, MA, and legislation.Communicate issues impacting release to management and supply chain.Promote GMP, GDP, and QMS within the site, seeking continual improvement in compliance and performance.Support investigations into quality non-conformances, complaints, recalls, and batch issues.Review and approve QMS documentation related to quality activities.Establish and monitor KPIs for quality activities, and oversee the site Change Review Board.Manage complaints and recalls, ensuring closure.Ensure timely completion of audits and support preparation for regulatory, company, and customer audits.Coordinate and ensure completion of site training on QMS processes and SOPs.Implement management review processes through group quality review meetings.Maintain accurate records of authorized activities.Stay updated on legislation, guidelines, and industry practices.Perform additional tasks as assigned by the line manager.What you need to apply:Eligible to be named on a manufacturer's license as a Qualified Person under EU Directive 83/EC.Minimum of 5 years' quality management experience in the pharmaceutical industry.Well-organized, with effective communication skills at all levels, reliability, IT literacy, and project management ability.
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