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Quality Coordinator

Job LocationCambridge
EducationNot Mentioned
Salary27,500 per annum
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

An opportunity has arisen within our Cambridge-based Regulatory, Medical and Quality Affairs Department which is responsible for regulatory compliance, generating technical evidence and maintaining the quality systems required for in vitro device manufactureand sales.Reporting to the QC/QA Manager, your role will predominantly focus on Quality Assurance activities responsible for the management and maintenance of the Quality Management System, ensuring compliance with established processes and assisting in process improvement.You will also support the QC Team Leader with document auditing, batch release of final products and manufacturing/test equipment maintenance.This is a key role in the roll-out of OGTs new electronic Quality Management System (eQMS). Your role will be pivotal in the establishment of a number of core processes to support the new eQMS functionality and in the review and continual improvement of existingprocesses as they are transferred to the new system.Quality Assurance duties will include:

  • Establishment and maintenance of QMS processes and process improvement
  • Coordination of customer complaints
  • Coordination of change control requests and non-conformances raised
  • Assisting in documentation control
  • Internal auditing
Quality Control duties will include:
  • Goods in testing of raw materials
  • Manufacturing and test equipment maintenance and calibration
  • Validation testing of new equipment
Quality Coordinator Requirements:
  • a BSc degree or equivalent in a science related subject, biology based or similar discipline
  • Demonstrable experience working in a Quality Assurance / Quality control role preferably within a highly regulated industry
  • Experience of working in a production or laboratory environment
  • Experience in the use of eQMS and internal auditing (desirable)
  • Good attention to detail and accuracy
  • Strong problem-solving skills
  • Ability to work to deadlines and as part of a team in a sometimes highly pressurised environment
  • Confidence to speak up and suggest process changes and improvements to deliver efficiency
About Oxford Gene Technology:Oxford Gene Technology (OGT) provides world class genetic research solutions to leading clinical and academic research institutions. We are a rapidly growing company with state-of-the-art facilities and over 100 employees based at our Cytocell office in Cambridgeand our head office in Oxford. With customers in over 60 countries worldwide and ambitious expansion plans, we have a strong reputation and increasing share in the large and growing genomic medicine market.Location: Cambridge Science ParkContract Type: PermanentHours: Full TimeSalary: Up to £27,500 per annumBenefits: Competitive salary, Pension Scheme (10% non-contributory), Private Health Insurance, 21 days holiday rising with service, High Street Discount Scheme.Closing date: 30th July 2021No agencies pleaseYou may have experience of the following: Quality Assessment Officer, Quality Assurance Officer, QA Officer, Internal QA Officer, Internal Auditor, Compliance Officer, Quality Assistant, Compliance Assistant, Quality Auditor, Compliance Auditor, Standards Officer,etc.

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