i-Pharm Consulting

QA Associate

Location
Stevenage
Salary
Negotiable
Posted
10 Jan 2019
Closes
24 Jan 2019
Ref
DWQAA1
Contract Type
Permanent
INTRODUCTION

i-Pharm Consulting are partnered with a revolutionary biotechnology organisation who are looking to strengthen their quality team with an ambitious QA Associate who wants to work at the forefreont of cutting-edge cell therapy treatments.

TITLE

- QA Associate

JOB SUMMARY

- Opportunity to lead cutting edge QA projects within Cell Therapy
- Truly unique biotech company
- Groundbreaking therapies within Autoimmune and Oncology
- Elite industry leaders and cohesive working environment
- Excellent scope for professional development

LOCATION

- Stevenage, 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 and UK regulaations
- Active collaboration with management for continual quality performance improvement for the overall function

REQUIREMENTS

- Relevant scientific degree
- 4+ years' experience within a regulated GMP environment
- ISO:9001, GMP knoweldge
- Proven QMS management
- 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 / Non-conformance / CSV / Equipment / Manufacture / Manufacturing / Facility / Utilities / Machinery / HVAC / CFR / Annex II / Annex 15 / Sterile / Biologics / Sterile / 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 / Hertfordshire / Stevenage / St Albans / London / Cambridge / Welwyn Garden City / Letchworth Garden City / Hitchin / Luton / Bedford / Bedfordshire / Hertford / Hatfield / Helem Hemptstead / Watford / Harlow / Enfield / Saffron Walden / Essex / Bletchley / Milton Keynes

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