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Heidi

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Design Quality Engineer
Seen active today Posted Aug 12
London, United Kingdom Mid Full Time

Role highlights

  • What you'll do Drive Medical Device Design Control Processes Lead the implementation and continuous improvement of design control processes…
  • Your core mission is to help ensure that our software design and development activities meet global medical device requirements, leading…

Leonardo UK Ltd

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Senior or Principal Quality Assurance Engineer
Seen active yesterday Posted Aug 13
Luton, United Kingdom Senior Full Time

Role highlights

  • Practical experience with Quality Tools including Root Cause Corrective Action, Pattern Fault Lifecycle, Process Mapping, Verification, and…
  • What you will do as a Quality Engineer: Act as the dynamic primary point of contact for quality-related matters with…

Leonardo UK Ltd

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Principal Quality Assurance Engineer
Seen active today Posted Aug 13
Luton, United Kingdom Senior Full Time

Role highlights

  • Practical experience with Quality Tools including Root Cause Corrective Action, Pattern Fault Lifecycle, Process Mapping, Verification, and…
  • What you will do as Principal Quality Engineer: Act as the dynamic primary point of contact for quality-related matters with…

Indra Group UK & Ireland

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Quality Engineer
Seen active today Posted Aug 12
Redhill, United Kingdom Mid Contract

Role highlights

  • Requirements Required Skills and Experience: Bachelor’s degree in Engineering, Quality Assurance, or a related discipline.
  • The Quality Engineer will play a key role in ensuring that all project deliverables meet the highest standards of quality,…

Medisafe UK Limited

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Senior Quality Engineer
Seen active today Posted Jun 30
Bishops Stortford, United Kingdom Senior Full Time

Role highlights

  • We are currently recruiting for Senior Quality Engineer vacancy.
  • Required Experience Min 5 years working experience of ISO13485 or similar Min 5 years working in manufacturing Data analysis experience…

Ultra Cyber Limited

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Project Quality Engineer
Seen active 3 days ago Posted Jul 24
Maidenhead, United Kingdom Mid Full Time

Role highlights

  • As Project Quality Engineer, you are responsible for developing and implementing project quality plans that meet business, customer and con…
  • Work with project, production and process teams to improve operating processes, product yields and overall quality performance.

NUVIA UK

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Quality Engineer
Seen active today Posted Jul 9
London, United Kingdom Mid Full Time

Role highlights

  • Proven experience working in a quality assurance/control environment within the nuclear industry or other relevant safety critical industry.
  • Experience of implementing a variety of quality related solutions.

Leonardo UK Ltd

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Quality Engineer
Seen active today Posted Aug 6
Luton, United Kingdom Mid Full Time

Role highlights

  • Working knowledge of quality tools like Root Cause Corrective Action (RCCA), Process Mapping, Verification, Pattern Fault Lifecycle, and Fi…
  • Support continuous improvement initiatives across production, engineering, and quality workflows.

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Ultra Cyber Limited

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Project Quality Engineer
Seen active 3 days ago Posted Jul 24
Maidenhead, United Kingdom Mid Full Time

Role highlights

  • As Project Quality Engineer, you are responsible for developing and implementing project quality plans that meet business, customer and con…
  • Work with project, production and process teams to improve operating processes, product yields and overall quality performance.

GKN Aerospace Careers

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Quality Compliance Engineer
Seen active today Posted Jun 25
Luton, United Kingdom Mid

Role highlights

  • The Quality Compliance Engineer will demonstrate strong communication skills, using active listening, thoughtful inquiry, and clear articul…
  • Working within a fast-paced aerospace manufacturing environment, you'll keep our Quality Management Systems (QMS) aligned to AS9100 and cus…

Stefan Yonov

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Quality Compliance Engineer
Seen active today Posted Jun 2
Woking, United Kingdom Mid

Role highlights

  • Planning and execution of activities associated with compliance to Quality Management System requirements and IATF 16949 standard. *.
  • Working within the Compliance team in the Quality Compliance and Change Management department where you will be responsible for: *…

LE4001 Imanova Limited

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Quality Coordinator
Seen active today Posted Aug 20
London, United Kingdom Mid Full Time

Role highlights

  • Under the direction of the GMP Quality Manager, you'll support compliance with company and regulatory GxP requirements by overseeing qualit…
  • As part of a small supportive team, you'll administer and maintain the Quality Management System (QMS) in accordance with company…

Insulet International Ltd.

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Global Product Monitoring Vigilance Report Writer
Seen active today Posted Aug 19
London, United Kingdom Mid Full Time

Role highlights

  • Partner with Quality, Regulatory Affairs, Customer Care, Manufacturing and Engineering teams globally.
  • Support Medical Device Reporting (MDR) and other global vigilance obligations.

Johnson & Johnson Services, Inc.

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Manager, Clinical QA Program Lead
Seen active today Posted Aug 19
High Wycombe, United Kingdom Senior Full Time

Role highlights

  • Job Function: Quality Job Sub Function: Clinical Quality Job Category: Professional All Job Posting Locations: Allschwil, Basel-Country, Sw…
  • Independently leads and manages the domain-specific compliance audit programs as laid down in a comprehensive audit schedule, through plann…

Masimo

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Specialist, Regulatory Affairs
Seen active yesterday Posted Aug 18
London, United Kingdom Mid

Role highlights

  • Working within a highly collaborative, international organization, the Regulatory Affairs Specialist will liaise closely with cross functio…
  • Support Regulatory Affairs team with day-to-day tasks, as needed Perform other duties or special projects as assigned.

Perrigo

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Senior Professional - Regulatory Affairs Lifecycle Management - Biocides
Seen active today Posted Aug 18
London, United Kingdom Senior

Role highlights

  • Competencies Regulatory Expertise: Recognised specialist with strong knowledge of biocides lifecycle requirements, technical documentation,…
  • Provide strategic oversight of biocidal product dossiers, authorisation files, technical documentation, supporting data packages and inspec…

GB01 Lonza Biologics plc.

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Lab Technician - Method Validation
Seen active yesterday Posted Aug 18
Slough, United Kingdom Mid Full Time

Role highlights

  • Consistently adhere to current Good Manufacturing Practice (cGMP) standards, quality requirements, and laboratory procedures.
  • Lab Technician (Method Validation) Location: Slough - This is a lab based role Laboratory Technician responsible for supporting laboratory…

Biibhr

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Senior Pharmacovigilance (PV) Scientist
Seen active yesterday Posted Aug 18
Maidenhead, United Kingdom Senior Full Time

Role highlights

  • Experience in interacting with cross-functional teams such as Clinical Development and Regulatory.
  • Collaborate with Global Safety Officers and Safety MDs on investigational programs, including clinical trial activities and safety committe…

UCB

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Senior Process Quality Excellence Specialist
Seen active today Posted Aug 17
Slough, United Kingdom Senior Full Time

Role highlights

  • You are going to report to the Head of Process Quality Excellence and maintain the audit and inspection enabler within…
  • Participate in Audit and Inspection planning with Global Quality.

Seqirus UK Limited

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GLP/GCLP Vendor Oversight and QA Lead (EU)
Seen active yesterday Posted Aug 17
Maidenhead, United Kingdom Senior Full Time

Role highlights

  • Lead the vendor lifecycle: due diligence, qualification, quality agreements, risk-based monitoring, issue management and continuous improve…
  • About the role Own quality oversight of external partners supporting nonclinical and GLP activities (CROs, laboratories, test facilities).

Amgen

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Senior Manager, Study Oversight Manager
Seen active today Posted Aug 17
London, United Kingdom Senior Full Time

Role highlights

  • You will drive cross-functional collaboration, supplier performance, issue resolution, and continuous improvement while developing and ment…
  • Strong life sciences/biopharma clinical trial experience, within biotech, pharma, or CRO environments.

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GSK

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Senior Director, Future CMC Dossier Strategy
Seen active today Posted Aug 14
London, United Kingdom Senior Full Time

Role highlights

  • Working across a complex global matrix, you will collaborate with teams spanning Regulatory Affairs, Physical Product Development, Quality,…
  • Extensive experience in CMC regulatory submissions, dossier content generation, and process optimization within the pharmaceutical or bioph…

Thermo Fisher Scientific

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Graduate Scientist - GMP QC - Client-dedicated
Seen active today Posted Aug 13
Stevenage, United Kingdom Entry Full Time

Role highlights

  • Summarized Purpose: This is an entry level / early career scientist role intended to provide extra capacity by focusing on…
  • After full GMP training and authorization, the successful candidates will: Perform routine QC testing, mainly: pH measurement Karl Fischer…

Vitabiotics

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Quality Operations Manager
Seen active today Posted Aug 12
London, United Kingdom Mid Full Time

Role highlights

  • Experience managing quality systems.
  • Provide QA oversight for manufacturing, packaging, warehouse, distribution, and outsourced activities.

Ergomed

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PV Officer (experience in Medical devices required)
Seen active today Posted Aug 10
London, United Kingdom Mid Full Time

Role highlights

  • You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.
  • Job Description Providing support to other activities undertaken by the project team on behalf of the client and the company…

More roles at Ergomed

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