RHL has a long-standing relationship with a leading UK based biopharma manufacturing company, which focus on unique life-saving vaccination products. Based on ongoing expansion they are recruiting for a Environmental Monitoring QC Manager to join their rapidly growing, stable Microbiology team.
Since being established in 2015, the company has doubled in size and is now someone to lead, motivate and manage the Environmental Monitoring Team, one of the QC Microbiology Units, which performs Environmental Monitoring (EM) of critical pharmaceutical manufacturing operations and supports the site's validation activities. The team also supports the EM programme, compliance and training across site to all functions by providing specialist training in microbiological environmental monitoring methods and water sampling. The team is also responsible in processing EM and water results and generating data summaries and reports.
Position: QC Team Leader
Job Type: Permanent
Salary: £30,000 - £40,000
In this role you will
Lead, motivate and manage the performance and output of the EM Team to ensure that the team objectives are met in a timely manner.
Identify and implement improvements to the sitewide EM programme.
Maintain training levels across site to the highest standard for EM and compliance.
Monitor, schedule and ensure efficient throughput of Environmental Monitoring and Water data.
Plan and organise schedules for EM Team to ensure adequate assistance is provided to support critical manufacturing processes.
Escalate, troubleshoot and provide solutions to any unexpected issues arising in the laboratory or during EM.
Perform monthly one-to-one meetings with team members, provide support and monitor their progression against set objectives.
Be involved in writing and updating standard operating procedures relating to environmental monitoring and water sampling.
Conduct investigations, initiate and execute CAPAs and Compliance Action Items in a timely manner. Additionally, generate, write and perform technical review/ approval of EM and validation reports, and result summaries systems.
Operate in compliance with SOPs, c/GMPs and other regulatory requirements.
Execute EM testing if required.
Support microbiological testing and result review/ verification if required.
They are looking for a highly motivated quality professional who must be educated to degree level in Microbiology or relevant life-sciences subject, equivalent level qualification or significant experience of working at a similar level in specialist area and ideally have a post graduate qualification in Microbiology. The candidate must have experience working in a pharmaceutical GMP environment and good knowledge and understanding of Environmental Monitoring in Sterile Manufacturing.
Please apply to Kellie Dance - firstname.lastname@example.org
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