Quality Engineer

Birmingham, West Midlands, England
Up to £35000 per annum + full benefits package
08 Jul 2019
22 Jul 2019
Dominic Williams
Quality, GMP
Full Time
Contract Type
Experience Level
Experienced (non-manager)


i-Pharm Consulting are partnered with a globally-renowned Medical Device company who are looking to strengthen their QA Division with the acquisition of multiple Quality Engineers at their state-of-the-art Midlands site. This is an outstanding opportunity for a GMP orientated professional from a regulated sector to take the next step in their Life Sciences career!


- Quality Engineer


- Pioneering Medical Device organisation
- World class facilities
- Elite industry leaders and cohesive working environment
- Opportunity to grow within the global business
- Excellent autonomy


- Birmingham, UK


- Ensuring the QMS is maintained in line with business manufacturing requirements for related regulatory standards
- Supporting continuous improvement and identifying opportunities to reduce variations for manufacturing processes
- Liaising with manufacturing teams to ensure ISO/GMP compliance
- Ensuring all manufacturing processes are compliant with both internal and external quality systems
- Ensuring all manufacturing aspects are fully compliant with FDA CFR 820 part 21
- Active collaboration with management for continual quality performance improvement for the overall function


- A Level or above
- 2+ years' experience within a regulated GMP environment
- 13485/ISO:9001, FDA CFR 820 part 21, QSR's experience
- NCR and CAPA experience
- Validation experience (desirable), e.g. cleaning, CSV, equipment, process, facilities
- Effective communication skills
- Ability to work alone or as part of a team

About i-Pharm Consulting

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance, Validation and Bioinformatics.


If you would like to discuss this vacancy further, please call Senior Consultant Dominic Williams on +44 (0)20 3873 7066, or email dwilliams@i-pharmconsulting.com. If this role is not suitable, Dominic is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


CAPA / QMS / Audit / Auditor / GxP / GCP / GMP / GLP / GDP / GDPR / SOP / Cleaning / Validation / CSV / Equipment / Manufacture / Manufacturing / Facility / Utilities / Machinery / HVAC / CFR / Annex II / Annex 15 / Medical Device / Sterile / Wet / Non-wet / Dry / Non Wet / Biologics / Microbiology / Microbiologist / IQ / OQ / PQ / cGMP / Author / SOP writing / SOP / SAE / Quality Assurance / QA / QA specialist / Compliance / V-Model / Manager / Leader / QC / Quality Assurance / Quality Control / Senior Manager / Senior Management / Pharmaceutical / Quality Engineer / QA Engineer / Validation Engineer / Biotechnology / NCR / CAPA / Leicester / Midlands / Coventry / Birmingham / Stoke / Stoke-on Trent / Walsall / Solihull / Wolverhampton / Kidderminster / Worcester / Shrewsbury / Rugby / Stafford

Similar jobs

Similar jobs