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Quality Engineer

Job in Basingstoke, Hampshire County, RG21, England, UK
Listing for: Adecco
Full Time, Contract position
Listed on 2026-06-05
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
  • Engineering
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 GBP Yearly GBP 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Quality Engineer

Location:

Remote (Occasional in-person meetings in Basingstoke)
Contract Length: 9 months
Hourly Rate: £27.00
Working Pattern:
Full Time (40 hours/week)

Are you ready to make a meaningful impact in the Life Sciences industry? Our client is seeking a dedicated Quality Engineer to join their high-performing team! This is an exciting opportunity to advance your career while contributing to solutions that make the world healthier, cleaner, and safer.

What You'll Do:
  • Quality Oversight:
    Conduct detailed documentation reviews and monitor processes to uphold the highest standards.
  • Compliance Maintenance:
    Support and maintain compliance with GMP/GxP, ISO, and other regulatory requirements.
  • Issue Investigation:
    Lead root cause analysis efforts to investigate quality issues effectively.
  • Change Management:
    Manage and support change control activities while assisting in internal and external audits and inspections.
  • Documentation:
    Author and review quality documentation such as SOPs and investigation reports.
  • Data Analysis:
    Perform data analysis, trending, and reporting of quality metrics.
  • Collaboration:

    Work closely with cross-functional teams to drive corrective and preventive actions.
  • Continuous Improvement:
    Support initiatives aimed at enhancing quality systems and processes.
Who You Are:
  • A Bachelor's degree in Life Sciences, Engineering, Chemistry, Biology, or a related technical field, with 5+ years of experience in quality assurance/control (or an advanced degree with 3+ years of relevant experience).
  • Experience in regulated industries (pharmaceutical, medical device, or biotech preferred).
  • Proficiency with quality management systems (Master Control, Document Control Systems) and CAPA processes.
  • Demonstrated expertise in root cause analysis, investigation techniques, and implementing corrective actions.
  • Strong knowledge of GMP/GxP regulations, ISO standards (9001/13485), and quality system requirements.
  • Excellent problem-solving skills and attention to detail.
  • Strong verbal and written communication skills with the ability to collaborate across various functions.

Adecco is a disability-confident employer.

Adecco Group UK & Ireland is an Equal Opportunities Employer.

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