CQV Project Manager
Wood PLC

Philadelphia, Pennsylvania

Posted in Engineering


This job has expired.

Job Info


Overview / Responsibilities

Our CQV group at Wood is growing and we are adding CQV Project Managers to lead our well respected and established teams. We are looking for candidates experienced in CQV/Validation within the pharmaceuticals, biopharmaceuticals, vaccines, and aseptic processing areas. If are interested in working with a global leader in life sciences and possess the skill and drive to flourish in a dynamic and exciting environment, apply today!

* In addition to candidates from the Northeast Region, we also welcome candidates from all regions to apply who are open to 100% travel to be on client sites (per diem included). *

Key Responsibilities

  • Lead and Manage CQV Projects/Teams
  • Define project scope requirements, schedules, and develop CQV strategies
  • Drive the successful completion of CQV projects
  • Integrate CQV into the project lifecycle, working with other disciplines, both internal and external.
  • Preparation and execution of CQV life cycle deliverables, VMP, CQVMP, URS/DR/DQ/Risk Assessments/CTP/FAT/SAT/IOQ/PQ/PV/TOPs/Final reports
  • Quality review of CQV deliverables generated by project team members
  • Able to read review and perform walk downs of P&IDs
  • Manage punch list and execute deviation resolution
  • Effectively interfacing and communicating with 3 rd parties, client and CQV project teams
  • Ability to multi-task and adjust priorities to meet aggressive project timelines
  • Use of test equipment as required.
  • Complete work at client sites, the ability to travel is essential
  • Ability to complete work remotely, as required


Skills / Qualifications

Skills/Qualifications
  • Degree in engineering (preferably) or life sciences or suitable industry experience
  • Minimum of 8 years of experience in CQV and/or Engineering
  • Strong and clear communication skills, both written and verbal
  • Ability to effectively interface with Wood management, co-workers, clients, vendors and subcontractors
  • Understanding with proficient knowledge of common unit operations and processes used in biopharma/pharmaceutical manufacturing
  • Thorough knowledge and practice of cGMPs as related to the pharmaceutical industry
  • Strong computer skills
  • Customer Service oriented
  • Ability to understand scope and work within scope
  • Ability to work safely and keep the safety of those around in mind
  • Ability to recognize hazards and communicate these to the appropriate individuals


Physical Requirements
  • While performing the duties of this job, the employee is frequently required to walk, crouch, sit, and stand and may require close vision work
  • Ability to work at an active construction site is required


Company Overview

Wood is a global leader in engineering and consultancy across energy and the built environment, helping to unlock solutions to some of the world's most critical challenges. We provide consulting, projects and operations solutions in more than 60 countries, employing around 45,000 people. www.woodplc.com

Diversity Statement

We are an equal opportunity employer that recognises the value of a diverse workforce. All suitably qualified applicants will receive consideration for employment on the basis of objective criteria and without regard to the following (which is a non-exhaustive list): race, colour, age, religion, gender, national origin, disability, sexual orientation, gender identity, protected veteran status, or other characteristics in accordance with the relevant governing laws.


This job has expired.

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