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CQV Manager  -  Mainland Europe

9789

Due to our continued growth across mainland Europe we are hiring a Manager to lead our CQV activities across multiple project locations.   

Category:
Engineer Microbiology & Biotechnology
Location:
Leinster
Years of Experience Req.:
10
Date Posted:
20/11/2019
Days Remaining:
79
Employment Type:
Contract
Education Level Req.:
Bachelors Degree

CQV Manager  -  Mainland Europe

 

Due to our continued growth across mainland Europe we are hiring a Manager to lead our CQV activities across multiple project locations.   

 

As European CVQ Manager you will lead all CQV activity for the region - including delivering our current projects, securing new opportunities and managing client and stakeholder relationships for our key clients.

 

Key Responsibilities :

 

  • Successful delivery of C&Q projects –project budgets, schedules, deliverables, quality, client satisfaction.
  • Manages and assigns resources to meet project requirements and to maintain targeted / budgeted utiliz840689.712668ation
  • Maintains contact with respective clients & stakeholders to assure customer satisfaction.
  • Supports business development strategies and activities - attending bid meetings, prepare proposals, proposal presentations
  • Develops and maintains network to develop opportunities.
  • Works with potential new and existing clients to initiate projects following current industry practices.
  • Fostering collaborative working between DPS teams, client teams, and sub-contractors
  • Leads, mentors, trains and manages team of C&Q staff assigned to the region.
  • Recruitment of new staff members in conjunction with HR partners
  • Special projects as assigned.

 

Desired Skills and Experience:

 

  • Degree level qualification, science or engineering discipline preferred.
  • Significant experience (10+ Years) of leading C&Q teams in the pharmaceutical industry including bio-pharmaceutical and utility qualification activities and documentation requirements
  • General exposure and experience in a GMP/Validation discipline with a knowledge and understanding of pharmaceutical Design/Construction/Commission/Validate processes and how they relate to regulatory requirements and GMP regulations within the E.U. and U.S. FDA.
  • Excellent communication & presentation skills, ability to influence, persuade, negotiate and compromise, lead and chair discussion.
  • Proficiency with Microsoft Office applications (Word, Excel, Project, PowerPoint, etc.).

 

About DPS

 

DPS is a leading Project Management and Engineering Company delivering Full Service Engineering with a ‘client first’ mentality and personal touch across a range of market sectors: Project and Programme Management, Procurement, Design, Construction Management, Health & Safety Management, Commissioning, Qualification and Start-up. We have one goal: to deliver more than our clients expect first time, every time.

 

We’ve been serving industry around the world for 40 years plus, relied on for our agility, original thinking, sound judgment and high-caliber people. What sets us apart is the rapport we build with our clients and the care we take to gain a fundamental understanding of our client’s businesses. We employ over 1600+ people out of our sixteen office locations and we serve a broad range of clients ranging from multinational companies to small generic producers

 

 

 

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