Average salary: £55,000 /yearly
More statsSearch Results: 2,315 vacancies
...LEX Diagnostics are recruiting for an organised Document Controller to join the team. In this role, you will be responsible for providing technical... ...with FDA approvals. You will receive support from the Quality Systems Manager and play an integral role as a valued member...
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Local area
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...Diagnostics is currently hiring for a Senior Quality Control Scientist to become part of our... ...chemicals are received, aliquoted, stored with documentation and uploaded to the Quality Management... ...all requirements of working in an ISO 13485/FDA regulated environment.
Adhere...
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...ensure key management decisions are made
AutoCAD) and other documentation of design and installation
Programme and facilitate the flow... ...Residential Projects
Willing to contribute and adhere to the quality and safety requirements of the operation
3D Personnel is...
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For contractors
For subcontractor
Work at office
...a great opportunity to work in close collaboration with both the Quality and Manufacturing teams. Core responsibilities will revolve around... ...the expectations of working under formal quality systems such as ISO 13485 and FDA regulations.
You come from and are seeking a...
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Permanent employment
£28k - £38k per annumEstimated
...Are you looking for a new role in Document Control? A new role has just landed at Randstad in Cambridge.
Position: Document Controller
Location: Cambridge, Cambridgeshire
Start date: February 2024
Duration: 8 months
Pay rate: upto £200 per day depending upon experience...
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..., providing operational support and training when needed to ensure successful adoption.
Maintain and improve data hygiene and quality control.
Identify opportunities for improvement and advancement.
Develop and maintain a deep understanding of the hospitality and travel...
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Afternoon shift
LEX Diagnostics is currently hiring for a Senior Quality Control Scientist to become part of our Production team. Reporting directly to the... ...reagents and chemicals are received, aliquoted, stored with documentation and uploaded to the Quality Management System (QMS) as required...
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...team to drive advancement of platform development developing methods for scalable, rigorous, and cost-effective manufacturing and quality control. The successful candidate will work as part of the team responsible for the development, characterization, and production of...
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Immediate start
...experiment throughput, measurement fidelity, and alignment with the figures of merit
Design data processing, data interpretation, and quality control algorithms for a broad range of analytical methods
Ideate and demonstrate opportunities to both improve data quality and...
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Immediate start
Senior Quality, GMP Operational Quality Specialist (On-Site) page is loaded Senior Quality... ...archival of batch records and other supporting documents in electronic Document Management System... ...activities including change control, and support of site programs.
Participate...
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Full time
Flexible hours
Afternoon shift
£85k - £100k per annum
...Type: Full-Time, Permanent
About the Role
A dynamic pharmaceutical company in Cambridge is seeking a Director of Quality Control. This role involves overseeing all QC activities, implementing and maintaining QC systems, and ensuring compliance with GMP and MHRA regulations...
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Permanent employment
Full time
£45k - £60k per annum
...role is for a highly experienced Quality Engineer who is passionate in... ...that quality requirements are documented, effectively communicated and... ...(e.g., IRCA Certified ISO 9001 Lead Auditor).
Demonstratable... ...activities as well as supporting control activities to ensure Quality...
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£40k - £53k per annumEstimated
...increases efficiency.
We’re now looking for a Quality Manager with experience leading a start-up through to ISO 9001 (or similar) to join our mission.... ...our QMS, you’ll set up and manage a version-controlled digital document management system.
You’ll be in a customer...
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Full time
Local area
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£45k - £60k per annum
...role is for a highly experienced Quality Engineer who is passionate in... ...that quality requirements are documented, effectively communicated and... ...(e.g., IRCA Certified ISO 9001 Lead Auditor).
~Demonstratable... ...activities as well as supporting control activities to ensure Quality...
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Permanent employment
Flexible hours
...analysis, meeting the rigorous standards required for FDA submissions.
Thrive in an ISO 13485 regulated environment, where your expertise contributes to maintaining exceptional quality control processes.
Take the lead in enhancing QA/QC Standard Operating Procedures and...
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Hourly pay
Permanent employment
Locum
...Reference: 35202
Polytec are looking for a Quality Engineer for our client based in... ...problems within production and assay teams (ISO 15189)
* Lead for the introduction of new... ...operations, inspection plan, production documentation and risk assessments
* Monitoring quality...
Permanent employment
Work visa
Working Monday to Friday
...Quality Engineer
Ely, Cambridge
Full Time Permanent role. Our Client based in the Ely, Cambridge... ..., reliable and honest.
* Maintain our current ISO 9001-2015 accreditation
* Maintain and update quality Documentation, including inspections records, reports and procedures...
Permanent employment
Full time
Flexible hours
Monday to Thursday
Quality Engineer - Cambridge - Medical Devices
We are currently looking for a Quality Engineer... ...Quality Assurance of Medical Devices to ISO 13485 standards, although knowledge of EN... ...creating technical files and testing documentation.
We would expect you to have a degree...
...Are you a Quality Engineer - Electronics looking for an exciting job opportunity in Cambridge... ...of high-performance Electronic Controllers for Lighting and recognition systems. For... ...own the QMS for the company standards to ISO 9001 and deliver quality products to the...
...suppliers to ensure the company's reputation and quality of products remain market leading.... ...plans and protocols for the product, documenting all activities within the Quality Management... ...prior experience with medical devices and an ISO 13485 environment, coupled with expertise...
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