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4 months ago
NOTE: Dalgety will not offer visa sponsorships to foreign national applicants and no immigration support is available.
Location: Near Burton on Trent, Staffordshire
About us:nWe are the UK Market leaders in the supply of pharmaceutical cannabis. We supply the medical community with the highest quality cannabinoids to improve the lives for UK Medical Cannabis patients.
About the job:nWe are looking for a highly motivated and driven candidate to join the QA department as an integral support function to achieve our mission to help our patients. We value and encourage learning and development.nAs the Quality Assurance officer you will support the QA Manager in overseeing GMP compliance, contribute to the management of QMS and ensure the maintenance of quality certifications and standards throughout the manufacturing, testing and release of the product.
Salary: £25-35k (dependent on relevant work experience)
Key responsibilities:
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Assist in maintaining the Company’s Quality Management system – including drafting of new procedures to enhance the companies QMS.n·
Support with assessment of deviation event investigations.n·
Support closure to plan of Change Controls and CAPA actions.n·
Issue, review and approval of GMP batch manufacturing records to support certification and release.n·
Assist in performance of internal self-inspection audits.n·
Support the Company’s Quality Meetings.n·
Assist in maintaining the Company’s quality certifications, e.g. GMP, GDP, HO approvals, etc.n·
Assist in preparation for inspections from MHRA and other Competent Authoritiesn·
Provide quality review and input to manufacturing and business activities.n·
Ensure compliance with the Company’s Quality Standards.n·
Engage with the wider team and sector to gain wider knowledge of the industry, changes in legislation and
working procedures affecting the environment of the Company.n·
Report to the QA Manager daily.n·
Provide support to other functions within the Company as requested.
Key skills/ Requirements:
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BSc in a relevant life-science subject (Biology, Chemistry or Pharmacy)n·
2+ years of hands-on Quality Assurance experience desirablen·
Hands on experience at a site holding GMP certification and licencing.n·
Experience in the quality sector in manufacturers of pharmaceutical products and/or APIs.
Who you are:n·
Excellent organisational skills, interpersonal and communication skills (written and oral) are essential.n·
Strong sense of professionalism.n·
Self-motivated and proactive including both defining and executing tasks.n·
Work collaboratively within a cross-functional team to deliver the highest standard of work.n·
Results oriented and efficient, with a strong focus on meeting targets and achieving goals.n·
Strong attention to detail.
Additional requirements:n·
Ability to attend domestic and international technical conferences/exhibits, as required.n·
Background and criminal record checks are a requirement for the role.n·
In order to fulfil the role within Quality Assurance, the jobholder must develop an up-to-date knowledge of
developing Quality Systems and their implementation / maintenance within the UK and EU
Travel Requirements:n·
Role is primarily office based.n·
We require an on site presence due to the responsibility of the role, so the candidate needs to be comfortable with commuting near Burton on Trent to be considered.n·
Travel is primarily: UK & Europe
How to apply:nAll applicants must
with a CV and a Cover Letter to apply.nDo not
apply via LinkedIn, we will only respond to applicants who email us.nThis role does not offer sponsorship.
