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Quality Assurance Officer

New Appointments Group·Sandwich (South East England)
£29 000 – £35 000 / year
Vox Summary
  • Role Responsibilities: Provide QA support, maintain the QMS, review documentation, assist with audits, product recalls, and manage training records.
  • Key Requirements: Minimum 3 years' QA experience in GMP pharmaceutical manufacturing, strong understanding of GMP and GxP, experience with QMS, CAPAs, Deviations, and Change Controls.
  • Conditions & Benefits: Full-time permanent position, salary up to £35,000/year, local candidates only, no restrictions on right to work.
Apply on sourceYou are leaving VoxJobs for reed.co.uk — the application is handled directly by the company. reed.co.uk

Job description

We are working with an established pharmaceutical company who are looking to employ a QA Officer, permanently in the Sandwich area. PLEASE DO NOT APPLY IF YOU DON'T LIVE LOCALLY TO SANDWICH, KENT AND HAVE A FULL RIGHT TO WORK WITH NO RESTRICTIONS (NO GRADUATE VISAS/SPONSORSHIP/RELOCATIONS PLEASE) This is an exciting full-time permanent position with a salary of up to £35,000/annum and a host of great benefits. Responsibilities: • To provide QA support to all departments. • Maintain and develop the Quality Management System. • Ensure all pre & post-production documentation is submitted to QA, checked and approved prior to use of any materials, and batch release. • Ensure all materials meet required specifications. • Complete QA review and approval of deviations, C.A.P.A's, change controls, complaints, out of specifications and other documentation such as SOP's and forms. • Assist with internal and external audits. • Assist with product recalls. • Ensure quality agreements and quality questionnaires are in place with external companies. • Manage and develop the company training matrix and complete quarterly reviews on employee training records. • Participate in weekly QA meetings. • Ensure investigations are carried out in a timely manner. • Develop and update logbooks as and when required. About You: • Minimum 3 years' Quality Assurance experience within a GMP pharmaceutical manufacturing environment • Strong understanding of GMP and wider GxP requirements • Experience of QMS, CAPAs, Deviations, Change Controls and batch record review • Excellent investigation and problem-solving skills • Ability to write clear technical reports and quality documentation • Strong organisational skills with the ability to prioritise multiple activities • Excellent communication skills and confidence working across all departments Local candidates need only apply and those with no restrictions on their right to work. New Appointments Group, Expertly Matching Employers and Jobseekers since 1975. y.fleming@newappointmentsgroup If this role isn't for you, please check out our website for other opportunities that may be suitable, or send us your CV, we'd still like to hear from you. You can find us on our website or on LinkedIn, Facebook, Instagram and X @nagrecruitment. We are committed to fostering a diverse and inclusive environment in line with the Equality Act 2010. All qualified applicants will be considered regardless of age, disability, gender reassignment, marriage or civil partnership, pregnancy or maternity, race, religion or belief, sex, or sexual orientation. New Appointments Group acts as an Employment Agency for permanent roles and as an Employment Business for temporary roles.

Transparency panel

Original source
reed.co.uk
Posted
Jul 13, 2026 · true date
Last verified
3 hours ago
Quality score
65/100
Salary stated30
Company identified0
applyUrl0
postedAt15
Complete description20

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