Barry-Wehmiller
Director, Compliance and Validation
Barry-Wehmiller, East Brunswick, New Jersey, United States
About Us:
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 office, part of a team of over 1,500 professionals across 45+ US offices
Role Overview:
Lead validation teams, develop project scopes, and support business development within the regulatory compliance practice, focusing on life sciences and FDA-regulated projects.
Key Responsibilities:
Lead validation professionals and interface with clients
Provide expertise in validation of utility, facility, and process equipment
Develop project scope statements, estimates, and proposals
Expand client engagements and support project delivery
Manage multiple projects ensuring objectives are met
Strengthen client and team relationships
Qualifications:
Minimum of 10 years' experience in validation/quality services within life sciences or biotech
Project management experience including scope, budget, schedule, and risk management
Experience leading CQV project teams and familiarity with validation of utilities, systems, and equipment
Ability to interpret engineering documents and develop proposals
Understanding of GMP, FDA validation, and data integrity standards
Strong communication, technical writing, and leadership skills
Bachelor's degree in engineering or related field
Willingness to travel for project needs
Additional Duties:
Advise management on processes and policies
Lead and direct team efforts, provide technical guidance
Ensure proper use of components, materials, and tools
Perform other duties as assigned
We encourage candidates from diverse backgrounds to apply and are committed to providing reasonable accommodations during the interview process. Barry-Wehmiller is an equal opportunity employer. Applicants may undergo pre-employment screening, including drug tests, background checks, and skills assessments.
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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 office, part of a team of over 1,500 professionals across 45+ US offices
Role Overview:
Lead validation teams, develop project scopes, and support business development within the regulatory compliance practice, focusing on life sciences and FDA-regulated projects.
Key Responsibilities:
Lead validation professionals and interface with clients
Provide expertise in validation of utility, facility, and process equipment
Develop project scope statements, estimates, and proposals
Expand client engagements and support project delivery
Manage multiple projects ensuring objectives are met
Strengthen client and team relationships
Qualifications:
Minimum of 10 years' experience in validation/quality services within life sciences or biotech
Project management experience including scope, budget, schedule, and risk management
Experience leading CQV project teams and familiarity with validation of utilities, systems, and equipment
Ability to interpret engineering documents and develop proposals
Understanding of GMP, FDA validation, and data integrity standards
Strong communication, technical writing, and leadership skills
Bachelor's degree in engineering or related field
Willingness to travel for project needs
Additional Duties:
Advise management on processes and policies
Lead and direct team efforts, provide technical guidance
Ensure proper use of components, materials, and tools
Perform other duties as assigned
We encourage candidates from diverse backgrounds to apply and are committed to providing reasonable accommodations during the interview process. Barry-Wehmiller is an equal opportunity employer. Applicants may undergo pre-employment screening, including drug tests, background checks, and skills assessments.
#J-18808-Ljbffr