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Job Details

Contract CQV Specialist – Dublin – Pharma Services

Company: i-Pharm Consulting
Location: Dublin
Reference: DAFE023
Closing Date: 14 Dec 16
Type: Contract
Salary (£): Negotiable
Benefits:

Job Summary:

CQV Specialist required for a leading Pharmaceutical Services Organisation. Contract opportunity for a CQV Specialist to carry out CQV lifecycle -project related activities for a biotech facility from Design through to Operational readiness. The methodology to be implemented is the Risk Based ASTM E2500 approach. Candidates must be eligible to work in the UK & Ireland.

Requirements:

Contract CQV Specialist – Dublin – Pharma Services

CQV Specialist required for a leading Pharmaceutical Services Organisation. Contract opportunity for a CQV Specialist to carry out CQV lifecycle -project related activities for a biotech facility from Design through to Operational readiness. The methodology to be implemented is the Risk Based ASTM E2500 approach. Candidates must be eligible to work in the UK & Ireland.

JOB TITLE
CQV Specialist / Commissioning, Qualification and Validation Specialist

LOCATION
Ireland / Dublin

LENGTH
18 Months initially

ROLE/DESCRIPTION

- Development of CQV plans and input to scheduling activities
- Implement the client CQV Program, ensuring a quality delivery
- Overview of protocol development and execution activities for the Design review, Installation Verification and Operational Verification aspects
- Planning, scheduling, and management of FAT attendance
- Oversight of Change Management activities during project lifecycle
- Summary Report writing/ metrics / schedule reviews
- Communicate with client representatives on project team, Engineering Team, Quality team and End Users during the different project phases

REQUIREMENTS

- A degree in science or engineering or equivalent
- Minimum of 7 years experience of C&Q activities in a large project environment within the pharmaceutical or biotech industries
- Knowledge of Biopharma processes using Single Use Technology
- Experience using the ASTM E2500 Risk Based Verification Methodology

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


TO APPLY

If you would like to discuss this vacancy further, please call 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

CQV Specialist / Commissioning, Qualification and Validation Specialist / Quality Engineer / Validation Engineer / Validation Specialist / ASTM / E2500 / Republic of Ireland / Ireland / Dublin / Cork

Apply for this job: Contract CQV Specialist – Dublin – Pharma Services

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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