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Head of QC

Posted 2 days 13 hours ago by Argenta

Permanent
Not Specified
Laboratory Jobs
Angus, Dundee, United Kingdom, DD2 5
Job Description
About the Role

A new opportunity has opened up for a Head of Quality Control at Argenta Dundee. This role will lead the site's Quality Control function, ensuring safe, compliant, and cost-effective testing and analytical activities while contributing to site strategy and performance delivery.

Experience
  • Pharmaceutical, laboratory or related environment awareness
Key Responsibilities
  • Key member of Site Leadership Team (SLT). Works with Site Senior Leadership Team to develop site strategy, implement site performance KPI's, and translate these into specific annual performance goals.
  • Overall responsibility for Argenta's Quality Control performance including testing of starting materials, finished products, stability samples, validation samples, data review and investigations.
  • Implements safe and GMP compliant working practices in the function, and ensures team perform their duties accordingly.
  • Lead the development of Argenta's Quality Control systems, ensuring on time delivery of valid results.
  • Drive staff engagement and a positive culture within the Quality Control department to achieve high-performing results.
  • Grow, develop and support your leaders and extended analytical staff.
  • Demonstrate leadership on quality, compliance and HS&E culture.
  • Management of QC budget.
  • Drive improvements in operational quality performance to enhance the customer experience and minimise the 'cost of poor quality'.
  • Provide QC support for analytical method transfers and Validation, ensuring a smooth introduction of new analytical methods, timely generation of data and ensure transfer documentation (protocols and report) are appropriately supported.
Qualifications
  • Bachelor's degree in Science (Chemistry; Pharmacy; Biology) or equivalent experience.
  • MSc. In Science, Pharmacy or Chemical Engineering, Pharmaceutical Technology or equivalent experience.
  • Minimum 5 years experience leading a QC laboratory function within a Pharmaceutical business with advanced knowledge of relevant cGMP requirements.
  • Experience in various analytical techniques, including method development, validation and transfer, wet chemistry and instrument techniques, chromatography systems and microbiological testing.
  • Well-developed leadership skills, with a proven track record of leading teams, performance management, and coaching.
  • Excellent interpersonal, written and verbal communication skills.
  • High energy and commitment to company values.
  • Commitment to continuous improvement and driving efficiency.
  • Technical writing skills e.g. reports; SOPs and change control.
  • Proven ability to evaluate and produce reliable results, troubleshoot, and problem solve complex problems.
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