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PCMC

Director, Compliance and Validation

PCMC, East Brunswick, New Jersey, us, 08816

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About Us:

Not sure what skills you will need for this opportunity Simply read the full description below to get a complete picture of candidate requirements. BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals from Strategy to Commercialization. As the only firm born from a manufacturing technology company to become an independent and fully integrated firm, we combine deep domain expertise in the manufacturing environment with an approach that is built to serve the dynamic needs of our clients. Rooted in our distinct culture of Truly Human Leadership, we cultivate the leaders who will define tomorrow and partner with our clients in the food & beverage, life sciences, industrial, and advanced technology industries to build the future of manufacturing and technology.

Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing technology for the packaging, corrugating, sheeting, and paper-converting industries. By blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world.

Job Description:

Position:

Director of Compliance & Validation, Life Sciences

Location:

Indianapolis, US

Overview:

Join our team to lead validation efforts in life sciences, working with industry experts to deliver high-quality solutions for clients in regulated environments.

What You’ll Do:

Lead validation teams and interface with clients

Provide expertise in validation of utility, facility, and process equipment

Develop project scopes, estimates, and proposals

Expand regional business development efforts

Manage multiple projects simultaneously

Ensure project objectives are achieved

Build strong client and team relationships

What You’ll Bring:

Minimum 10 years of experience in validation/quality services within FDA-regulated projects

Project management experience including scope, budget, schedule, and client management

Experience leading CQV project teams in validation of utilities, systems, and manufacturing processes

Ability to interpret engineering documents and develop proposals

Knowledge of validation methodologies and industry standards (preferred)

Understanding of cGMP, FDA validation, data integrity, and automation concepts

Strong technical writing and project management skills

Bachelor’s degree in engineering or related field

Willingness to travel as needed

Additional Responsibilities:

Advise management on processes and policies

Lead and guide engineering teams

Ensure optimal use of resources

Perform other duties as assigned

We encourage candidates from diverse backgrounds to apply and offer accommodations during the interview process. Barry-Wehmiller is an equal opportunity employer, using E-Verify, with pre-employment screening including drug tests, background checks, and skills assessments.

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