{
  "job_id": "ZU06FkUS-6CCkadqAAAAAA==",
  "job_city": "Cambridge",
  "job_state": null,
  "job_title": "Quality Engineer",
  "job_salary": null,
  "job_country": "GB",
  "job_benefits": null,
  "job_latitude": 52.254867,
  "job_location": "Histon",
  "job_onet_soc": "17211200",
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      "publisher": "Women For Hire - Job Board",
      "apply_link": "https://jobs.womenforhire.com/job/united-kingdom/histon-eng/quality-engineer-072446/?utm_campaign=google_jobs_apply&utm_source=google_jobs_apply&utm_medium=organic"
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      "publisher": "Women For Hire - Job Board",
      "apply_link": "https://jobs.womenforhire.com/job/united-kingdom/histon-eng/quality-engineer-072446/"
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  "employer_logo": null,
  "employer_name": "Talentmark",
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  "job_longitude": 0.103712,
  "job_posted_at": "17 days ago",
  "job_publisher": "Women For Hire - Job Board",
  "job_apply_link": "https://jobs.womenforhire.com/job/united-kingdom/histon-eng/quality-engineer-072446/?utm_campaign=google_jobs_apply&utm_source=google_jobs_apply&utm_medium=organic",
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  "job_description": "Talentmark is recruiting for a Quality Engineer to join a company in the pharmaceutical industry on a contract basis for 12 months. This is a hybrid role with 50% onsite in Cambridge.\n\nSalary:\n\nUp to £26.69 per hour PAYE or up to £34.54 per hour via umbrella company.\n\nQuality Engineer Role:\n\nLead design control and risk management activities for combination product development programs.\n\nSupport effective risk management activities at external design companies and manufacturing facilities.\n\nEnsure combination product development activities are compliant with all required standards.\n\nSupport the generation of all regulatory submission data.Your Background:\n\nHold a relevant scientific degree or have equivalent working experience.\n\nWorking knowledge of ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation.\n\nExperience in design controls and risk management for combination products.\n\nFamiliar with device assembly manufacturing processes.\n\nUnderstand Good Manufacturing Practices (GMP).Company:\n\nOur client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines, and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.\n\nApply:\n\nFor more information, or to apply for this Human Factors Quality Engineer please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (phone number removed).\n\nIt is essential that applicants hold entitlement to work in the UK\n\nPlease note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check",
  "job_google_link": "https://www.google.com/search?q=jobs&gl=gb&hl=en&udm=8#vhid=vt%3D20/docid%3DZU06FkUS-6CCkadqAAAAAA%3D%3D&vssid=jobs-detail-viewer",
  "employer_website": "https://www.talentmark.com",
  "job_onet_job_zone": "4",
  "job_salary_period": null,
  "job_apply_is_direct": false,
  "job_employment_type": "Contractor",
  "job_employment_types": [
    "CONTRACTOR"
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  "job_posted_at_timestamp": 1772582400,
  "job_posted_at_datetime_utc": "2026-03-04T00:00:00.000Z"
}