About The Position

Wood PLC serves the Pharma-Bio, Oil & Gas, Federal, Infrastructure, Manufacturing, Mining, and Power Industries globally. Our Philadelphia office is a center of excellence for our global Life Sciences network, providing process engineering, process design, and commissioning - qualification - validation (CQV) services to pharmaceutical/biotechnology clients worldwide. We support a facility's entire life cycle to bring life-saving therapeutics from concept through fruition. Our growing CQV group is seeking experienced Senior CQV Specialists in commissioning, qualification, and/or validation within the pharmaceuticals, biopharmaceuticals, vaccines, and aseptic processing areas. This position offers a competitive salary, opportunity for growth, and a 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.

Benefits

  • competitive salary
  • opportunty for growth
  • signing bonus
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