Social network you want to login/join with:Team 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's 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 utilize 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 product throughput.Perform QP certification of products for release to market, as necessary, to meet business requirements and in accordance with the release schedule.Manage site quality operations and batch certification, coordinating activities to ensure compliance and timely batch release.Review (or delegate) batch documentation, confirm certification of product batches in accordance with GMP, MA, and legislation, and record in the QP register.Communicate issues impacting release to management and supply chain.Promote GMP, GDP, and QMS within the site, seeking continuous improvement in compliance and performance.Support investigations related to non-conformances, complaints, recalls, and batch issues.Review and approve QMS documentation related to quality activities.Establish and monitor KPIs for all quality activities and oversee site audit programs.Coordinate complaint management and recalls, ensuring closure.Support preparation for regulatory, company, and customer audits, ensuring timely responses and actions.Implement and oversee training programs on QMS processes and SOPs.Conduct management reviews through tiered meetings.Maintain accurate records of authorized activities and stay updated on legislation and industry practices.Complete additional tasks as assigned by the line manager.What you need to apply:Eligibility to be named on a manufacturing license as a Qualified Person under EU Directive 83/EC.Minimum of 5 years' quality management experience in the pharmaceutical industry.Strong organizational, communication, IT literacy, and project management skills.
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