CQV Project Manager (Client site based) at Wood PLC in Rensselaer, New York

Job Description:

JOB DESCRIPTION



Wood PLC, on a global scale, serves the Pharma-Bio, Oil & Gas, Federal, Infrastructure, Manufacturing, Mining, and Power Industries. Our Philadelphia office has become the center of excellence for our global Life Sciences network. It provides process engineering, process design, and commissioning - qualification - validation (CQV) services to pharmaceutical/biotechnology clients worldwide. For projects of every scale, we provide services that support a facility's entire life cycle to bring life-saving therapeutics from concept through fruition. Learning from our team of industry-leading experts in facility design, regulatory standards, and project management will pay dividends toward your future career.

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 commissioning, qualification and/or 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!



RESPONSIBILITIES



Key Responsibilities

• Lead and Manage CQV Projects/Teams.
• Manage 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 3rd 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.

• 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 while manage project scope and schedule with drive to achieve both.
• Ability to work safely and keep the safety of those around in mind
• Ability to recognize hazards and communicate these to the appropriate individuals

• 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