Job Description

CQV Engineers / CQV Consultants Locations: Across Europe (Ireland, UK, Netherlands, Belgium, Germany, Switzerland, Spain, France, Italy, Denmark and more) Contract & Permanent Opportunities Available soon.

We are building a network of experienced CQV professionals across Europe to support current and future projects within the Pharmaceutical, Biotechnology and Medical Device sectors.

As a CQV professional, you will support commissioning, qualification and validation activities for GMP-regulated facilities, equipment, utilities, systems and processes. You will work closely with project, quality, engineering and operations teams during project delivery, start-up and regulatory readiness phases.

Typical Responsibilities

Develop and execute Commissioning, Qualification and Validation documentation
Author IQ, OQ and PQ protocols and reports
Support FATs, SATs and vendor testing activities
Execute commissioning and qualification activities on-site
Perform system walkdowns and punch-list management
Review URS, FRS, DDS and technical specifications
Support GMP compliance and regulatory requirements
Investigate deviations and support CAPA activities
Work across process, clean utility, facility and automation systems

Requirements

Degree in Engineering, Life Sciences or similar discipline
Experience within Pharmaceutical, Biotech or Medical Device environments
Experience with GMP-regulated projects
Knowledge of IQ/OQ/PQ methodologies
Experience with utilities, equipment, facilities, automation or CSV preferred
Ability to work on-site and travel across Europe when required

Highly Sought-After Experience

Sterile manufacturing
API facilities
Fill Finish projects
Clean Utilities
HVAC Qualification
CSV / CSA Validation
DeltaV, Siemens PCS7, Rockwell or SCADA Systems
Annex 1 and FDA regulated environments

Data Centre Commissioning Engineers / Commissioning Managers

LinkedIn Pipeline Job Description

Data Centre Commissioning Engineers & Commissioning Managers Locations: Across Europe (Germany, Ireland, Netherlands, Sweden, Denmark, Spain, Italy, Switzerland and more) Contract & Permanent Opportunities Available

We are actively building our network of Commissioning professionals supporting hyperscale, colocation and mission-critical Data Centre projects across Europe.

This is an excellent opportunity for experienced Commissioning Engineers, Cx Managers, Lead Cx Engineers and Commissioning Agents looking to support some of Europe's most exciting data centre developments.

Typical Responsibilities

Lead and support commissioning activities across mission-critical systems
Execute and review commissioning procedures and test scripts
Coordinate FATs, SATs and Integrated Systems Testing (IST)
Verify installation and functionality of electrical and mechanical systems
Manage commissioning schedules and stakeholders
Review technical documentation and design packages
Support handover activities and final client acceptance
Work closely with contractors, vendors and end clients

Requirements

Degree or trade qualification in Engineering
Experience commissioning data centre infrastructure
Strong understanding of electrical and/or mechanical systems
Experience with FAT, SAT and IST activities
Familiarity with commissioning methodologies and documentation
Ability to work on site and travel across Europe

Highly Sought-After Experience

Hyperscale Data Centres
Colocation Facilities
MV/LV Electrical Systems
UPS Systems
Generators
BMS / EPMS
Chilled Water Systems
CRAH/CRAC Units
Integrated Systems Testing (IST)
CxA or Commissioning Management experience

Qualifications & Requirements

Bachelor of Science in Engineering.
2+ years of relevant experience, years of experience will determine level of role suited to you.
Experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA.

Preferred Qualifications

Experience in writing and execution of PFC, FC, IQ, OQ, and PQ forms/protocols for GMP Utilities, Equipment, Systems, and Software.
General exposure and experience in a GMP/Validation discipline with a knowledge and understanding of
pharmaceutical Design/Build/Commission/Validate processes and how they relate to regulatory requirements and cGMP regulations within the E.U. and U.S. FDA.

Physical Demands

Must be able to: stand, sit, and walk for prolonged periods, stoop, kneel, crouch, and crawl as required.
Must be able to lift and move objects weighing up to 50 pounds and climb ladders as necessary.

Work Environment

Can work in both indoor and outdoor environments, which may include exposure to varying working conditions.
Can adhere to strict cleanroom gowning protocols.

Travel

This position will have up to 100% travel, or as required by the assigned project.
Position may be assigned to the client site for an extended period of time.
Overnight travel or staying in the city of the Client’s location is possible, depending on the assignment.
Travel will be per the IPS Travel Policy, client-specific travel policy, or project-specific travel plan.
Must have access to reliable transportation.

Safety

This position is a safety-sensitive position.
The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research, or other "non-administrative" areas.

All interviews are conducted either in person or virtually, with video required.

About Us

IPS, a Berkshire Hathaway company, is a global leader in technical consulting, architecture, engineering, procurement, construction management, commissioning, qualification, and validation services for technically complex facilities. Integration is how we think and work. It requires the ability to unite existing and emerging technologies into a process that reliably delivers products and accelerates speed to market. That end-to-end mindset allows us to be agile and anticipate challenges as we move projects toward operational readiness. IPS applies design and delivery expertise, client-side experience, and supplier-side insight to every project. We infuse our curiosity, our passion, and our commitment to partnership in delivering solutions at any scale. We meet our clients where they are and get them to where they need to go. That’s only possible when we care as much as our clients do.

Specialties

Process Architecture, Process Design, Engineering, Construction, Commissioning, Qualification, LEAN Project Delivery, Strategic Master Planning, Energy Conservation Management, Project Controls, Program/Project Management, Operations/Logistics Strategy and Planning, EPCMV, and Staffing Services.

All qualified applicants will receive consideration for employment at IPS without regard to race, creed, color, religion, national origin, sex, age, disability, sexual orientation, gender identity or expression, genetic predisposition or carrier status, veteran, marital, or citizenship status, or any other status protected by law. IPS is proud to be an affirmative action and equal opportunity employer.

Connect With Us!

If you do not meet the qualifications for this specific role, but would like to submit your resume for general consideration, please click here!

Pipeline for CQV Talent - Europe

Job Description