Validation Manager – 3 Month Contract – Medical Devices

Contract | New England, ENGLAND | 4 months | Deadline: 05 Mar 2018
This position has expired. Do not apply!

Job Summary

Contract
; Negotiable
New England
i-Pharm Consulting

£42,326 Average salary of similar jobs | Check Salary...

Job Description


Job Details
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Job 272 of 1000
Validation Manager – 3 Month Contract – Medical Devices

Company: i-Pharm Consulting
Location: South East England
Reference: DAFE0121
Closing Date: 05 Mar 18
Type: Contract
Salary (£): Negotiable
Benefits:


Job Summary:

My Client is looking for a Validation Manager to come in on short notice and have the experience to lead a team responsible for the continued development and management of the validation strategy that is in line with the group quality management system. Role involves large amount of cross functional collaboration with quality and technical departments to ensure the company remain compliant in this area. Candidates must be eligible to work in the UK.


Requirements:

Validation Manager – 3 Month Contract – Medical Devices
My Client is looking for a Validation Manager to come in on short notice and have the experience to lead a team responsible for the continued development and management of the validation strategy that is in line with the group quality management system. Role involves large amount of cross functional collaboration with quality and technical departments to ensure the company remain compliant in this area. Candidates must be eligible to work in the UK.
JOB TITLE
Validation, cGMP, Quality, Manufacturing
LOCATION
UK / South East
RATE
£Neg
LENGTH
3 Months
ROLE/DESCRIPTION
The selected Validation Manager will lead a team responsible for the continued development and management of the validation strategy that is in line with the group quality management system. Role involves large amount of cross functional collaboration with quality and technical departments to ensure the company remain compliant in this area.
REQUIREMENTS
You will need strong Medical Device validation and manufacturing experience with a good knowledge of cGMP, quality and regulatory requirements. Experience of direct involvement with regulatory inspections will also be strongly preferred.
TO APPLY
If you would like to discuss this vacancy further, please call Senior Recruitment Consultant David Fearnley on +44 (0)20 3189 0497, or email dfearnley@i-pharmconsulting.com. If this role is not suitable, David is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Validation, Validation Manager, cGMP, GMP, manufacturing, South East, Pharmaceutical, Medi Device, Medical Device
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 and Bioinformatics.
www.i-pharmconsulting.com


Contact Information:
Address:  Head Office
212 New King’s Road London
SW6 4NZ
England
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

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