Quality Engineer

Location
Birmingham, West Midlands, England
Salary
Up to £35000 per annum + full benefits package
Posted
08 Jul 2019
Closes
22 Jul 2019
Ref
QADAW7
Contact
Dominic Williams
Discipline
Quality, GMP
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

INTRODUCTION

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!

TITLE

- Quality Engineer


JOB SUMMARY

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


LOCATION

- Birmingham, UK


RESPONSIBILITIES

- 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

REQUIREMENTS

- 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.
www.i-pharmconsulting.com


TO APPLY

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.

KEY WORDS

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

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