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C&Q Project Engineer job in Birmingham

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Job Ref:  204748480
Employer:  cv-library.co.uk
Industry:  Civil and Structural
Job Type:  Permanent
Country:  United Kingdom
City:  Birmingham
Post Code:  B12
07/10/2016 04:23
PM Group is an international engineering, architecture and project management firm. We collaborate with many leading private companies and major public sector organisations, and are currently involved with 30 major projects throughout Europe, Asia, USA and the Middle East. Established in 1973, PM Group now employs over 2,100 people, based in
25 locations worldwide. Our areas of specialty are in the Pharmaceutical,
Bio-pharmaceutical, Food & Beverage, Advanced Manufacturing, Healthcare, Education, and Energy sectors.

We wish to recruit a high calibre CQV Project Engineer to be based out of our Birmingham Office. Reporting to the C&Q Department Manager, the
successful candidate will ideally coming from a Pharmaceutical industry
background and will have good knowledge of lifecycle Validation procedures and GMP

Job Role and Responsibilities - will include but not be limited to:

• Prepare C&Q plans in line with the strategic goals of the Client and to
manage timely and compliant delivery of the plan. To co-ordinate and
align the activities of the plan aligned with client engineering, quality
and production requirements.
• Liaise with all departments necessary for delivery of the project. Close
liaison is required between Design, Engineering, Procurement and
• Develop and execute Commissioning & Qualification Protocols as
• Lead C&Q projects, on behalf of the C&Q Department, as directed and
as appropriate. Assist with alignment between the C&Q Project teams
and client expectations.

Qualifications and Experience:

• Bachelor Degree in Engineering or equivalent
• Hands-on experience of C&Q activities within a pharmaceutical
environment, with an ability to translate Client strategic goals in to
practical plans for project C&Q activities
• Familiar with and conversant in Current GMP & Engineering Guidelines
pertaining to UK/Europe/USA e.g. ICH, MHRA 'Orange Guide', ISPE,
Experienced in Qualification of:
o Manufacturing Equipment
o Utilities i.e. Highly Purified Water, Process Gasses
o Facilities i.e. Cleanrooms, HVAC
o Control Systems i.e. SCADA, DCS, PLC etc.
• Be able to demonstrate ability to write and execute suitable
documentation and Protocols including:
System Impact Assessments, URS, VMP, DQ, IQ, OQ and Reporting
• Proven successful track record in FDA/MHRA Inspections preferable
• Experience in implementing C&Q policies and procedures
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