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  

• 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

Diversity Statement (EEO)  

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.