CQV Senior Project Manager

Job Description

Remarkable people, trusted by clients to design and advance the world.

Wood is recruiting for a CQV Project Manager to join its Life Sciences business. This opportunity is Hybrid.

The Role

Wood is currently seeking a highly motivated CQV Senior Project Manager to join our Morrisville, NC which provides process engineering, process design, and commissioning - qualification - validation (CQV) services to pharmaceutical/biotechnology clients worldwide. The CVQ Project Manager will lead our well respected and established teams. We are looking for a candidate experienced in commissioning, qualification and/or validation within the pharmaceuticals, biopharmaceuticals, vaccines, and aseptic processing areas.

Our Clients and Projects

Designing the future. Transforming the world .

Wood’s Life Sciences business leverages 50 years of Life Sciences experience in the Americas, Europe and Australia. We bring full asset lifecycle value proposition to leading pharmaceutical and biotechnology companies by accelerating the design and delivery of their most complex facilities at pace with uncompromising quality and safety standards. Our future-minded team focuses on sustainability and optimized facility performance through innovative and cleaner design solutions that ultimately lead to positive advancements in human health.

What We Can Offer

• Meaningful and interesting projects delivered to leaders of industry across Life Sciences sector.
• Flexible working arrangements that balance client, team and individual needs offering hybrid working.
• Commitment to Diversity and Inclusion; we are an organization actively committed to diversity and inclusion across our business with employee networks committed to giving all employees a voice.
• Competitive salary with regular salary reviews to ensure we are rewarding at the right level in line with the market.
• Flexible benefits package that can be adapted to suit your lifestyle.
• Commitment to continued professional development; development plans that are tailored to your individual needs and interests.
• Global connections: join experts around the world who are at the leading edge of our industry, shaping the standards of our profession.
  
  

Responsibilities

Typical 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.
  
  

Applicants must be authorized to work lawfully in the US without sponsorship from Wood, now or in the future.

Qualifications

What makes you remarkable?

At Wood, we are committed to equal opportunities and welcome all talented individuals to consider joining our team. So even if you don't match every statement below but feel you have some of the experience, knowledge or skills needed for this role, we encourage you to apply. It will take all of us working together to deliver solutions to the world’s most critical challenges.

Expected

• 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.
  
  

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

About Us

Wood is a global leader in consulting and engineering, helping to unlock solutions to critical challenges in energy and materials markets. We provide consulting, projects and operations solutions in 60 countries, employing around 35,000 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.