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 career. Our CQV group at Wood is seeking a regional Director of CQV , open to various locations in the United States. The position will be responsible for the regional development, maintenance, and growth of the CQV business. Primary responsibilities include CQV business development, building a local CQV group (recruiting, interviewing, hiring, team performance), identifying commissioning, qualification and/or validation opportunities, proposal development, project execution, and full responsibility for the profit and loss regional CQV business. This is a seller-doer position . As a candidate you must have the ability to identify opportunities, develop the team, and assist in project execution. Previous experience as an Engineering/CQV service provider preferred. Must be thoroughly knowledgeable in pharmaceutical industry cGMPs, commissioning, qualification, validation, and CQV project management. Must have proven capability in leading project teams, scheduling, coordinating the efforts of a multidisciplinary team and identifying and building client relationships. Ability to effectively interface directly with clients in representing Wood is essential. This position offers a competitive salary, opportunty for growth, and a signing bonus.
Requirements
- Ability to travel to client sites
- Business development including identifying potential growth areas and development of CQV proposals
- Extensive experience in commissioning/qualification/validation and a thorough understanding of cGMPs
- Knowledge of the local pharma market
- BS Engineering (Chemical Engineering preferred); Other life sciences may be acceptable; Educational requirements may be relaxed for suitable experience
- Minimum of 12 years of experience in engineering, commissioning, qualification, and validation primarily in the field of pharmaceuticals
- Must be thoroughly knowledgeable in pharmaceutical industry cGMPs, commissioning, qualification, validation, and CQV project management.
- Must have proven capability in leading project teams, scheduling, coordinating the efforts of a multidisciplinary team and identifying and building client relationships.
- Ability to effectively interface directly with clients in representing Wood is essential.
Nice To Haves
- Previous experience as an Engineering/CQV service provider preferred.
Responsibilities
- CQV business development
- building a local CQV group (recruiting, interviewing, hiring, team performance)
- identifying commissioning, qualification and/or validation opportunities
- proposal development
- project execution
- full responsibility for the profit and loss regional CQV business
- Effectively lead project teams managing scope, budget, and schedule to ensure project success
- Fostering Wood’s relationships with clients
- business development
- Hiring of CQV personnel
- Ability to lead and or assist in project execution
Benefits
- competitive salary
- opportunty for growth
- signing bonus
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What This Job Offers
Job Type
Full-time
Career Level
Director
