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 utilize QP eligibility and leadership experience in a Head of QA position overseeing Quality Assurance and Quality Control Teams.Highly competitive salary and benefits on offer.What you will be doing:Ensure an appropriate, compliant QMS is in place to ensure site compliance, regulator inspections, and product throughput.Perform QP certification of products for market release, aligning with business needs and release schedules.Manage site quality operations and batch certification, ensuring compliance and timely release.Review batch documentation and certify batches 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 continuous improvement.Support investigations related to quality non-conformances, complaints, recalls, and batch issues.Review and approve QMS documentation related to quality activities.Establish and monitor KPIs, manage the site Change Review Board, and maintain technical agreements.Manage complaints and recalls, ensuring closure.Complete internal and external audits as scheduled.Assist in preparing for regulatory, company, and customer audits, ensuring timely responses and actions.Ensure availability and completion of site training on QMS processes and SOPs.Implement management review processes through group quality review meetings.Maintain accurate records of authorized activities and stay current with legislation and industry practices.Perform additional tasks as assigned by the line manager.What you need to apply:Eligible to be named on a manufacturing license as a Qualified Person under EU Directive 83/EC.At least 5 years of quality management experience in the pharmaceutical industry.Well-organized, effective communicator at all levels, reliable, IT literate, and capable of managing projects to deadlines.
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