Senior CQV Specialist (Client based - various locations)

Wood•Novato, CA

13h•Remote

About The Position

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 engineering career. Our CQV group at Wood is growing and we are adding to our well respected and established team of Senior CQV Specialists. We are looking for candidates experienced in commissioning, qualification and/or validation within the pharmaceuticals, biopharmaceuticals, vaccines, and aseptic processing areas. If you 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! This position offers a competitive salary, opportunity for growth, and potential signing bonus.

Requirements

Degree in engineering (preferably) or life sciences or suitable industry experience.
Minimum of 5 years of direct 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 advanced knowledge of common unit operations and processes used in biopharma/pharmaceutical manufacturing.
Thorough knowledge 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.

Responsibilities

Preparation and execution of CQV life cycle deliverables, URS/DR/DQ/Risk Assessments/CTP/FAT/SAT/IOQ/PQ/PV/TOPs/Final reports
Ability to work independently and direct the work of junior team members
Ability 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 100% of the time is essential.
Ability to complete work remotely, as required.