Director, Compliance and Validation

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:

• Director of Compliance & Validation, Life Sciences

  Who You’ll Work With 
   
  You will join our East Brunswick, New Jersey office, be part of a committed organization of over 1,500 professionals, and work in teams and directly with our clients doing work that is shaping the world around us. You will be welcomed into a rapidly growing business and team and empowered to make an impact. You will be valued, cared for, and challenged on your path to becoming a world-class professional consultant and surrounded by leaders who are committed to creating an environment that enables you to realize your own success and fulfillment. 
   
  When you join BW Design Group as a Director of Compliance & Validation, Life Sciences, you are joining a team that will challenge you and position you for growth. In this role, you will work with a team of industry experts to help the world’s leading companies solve their most difficult problems. You will join our Regulatory Compliance Practice and partner with seasoned leaders, technical specialists, and subject matter experts to deliver the highest quality solutions to our clients with consistency and accuracy. 
   
  What You’ll Do 
   
  You'll work individually and in teams to support capital projects and implement solutions for our clients. Together, you will help our clients make critical changes to improve their performance and realize their most important goals. 
   
  As the Director of Compliance & Validation, Life Sciences, you will be responsible for leveraging their past professional experiences, along with BW Design Group’s engineering offering to expand our presence in the Life Science market sector in New Jersey. This role will lead a Regulatory Compliance Validation team for pharmaceutical, biotech and medical device manufacturing projects for our clients. 
   
  We seek a passionate, high achieving professional who thrives in a fast-paced, collaborative, entrepreneurial environment. A leader, mentor, coach with infectious enthusiasm who lifts others to his/her level and exhibits uncompromising dedication to client welfare. A subject matter expert who fully understands validation and regulatory compliance and can work with clients to develop diverse solutions to their problems. They also need to meet client needs and guide them in industry leading best practices for complex projects that require these scope services. Actively be involved in the execution and leading of all phases of projects. 

  • Lead with an uplifting entrepreneurial spirit 

  • Inspire excellence in all aspects of performance and project execution 

  • Display enthusiasm and excitement for client projects that lifts project teams to high levels of job satisfaction 

  • Consistently seek new value-add opportunities for clients and BW Design Group 

  • Meet with clients to define the program requirements based on an understanding of the client's production process flow and space environmental needs derived from meetings with the client and the review of any documentation provided by the client 

  • Assess the requirements of a project, break a project into tasks, and work with teams to determine scope of work, budget and staffing 

  • Communicate and interact directly with clients in a collaborative and professional manner 

  • Create integrated solutions and communicate key concepts to the client 

  • Develop the base plan and coordinate technical requirements with engineering disciplines 

  • Understand and develop design intent based on client objectives and provide excellent client service 

  • Research material options to deliver an optimal solution for the client when required by project scope 

  • Assign and review work of project team. 

  • Check progress of work and alert project leads to change of scope or additional services. 

  • Coordinate all aspects of project document completion within company and externally with clients and other design professionals. Proficient written and oral communications skills. 

  • Prepare or review budgets based on experience and scope of project. 

  • Assist in the education and development of the team and act as resource for questions. 

  • Innovate and improve design and service delivery method and processes 

  • Build and sustain long term client and internal relationships 

  • Participate actively in relevant industry organization events and conferences 

  • Make an impact day-to-day with your skills and expertise, strengthening that relationship with our clients and team  

   

  What You’ll Bring 
   

  • A passion for a career in the Life Science industry 

  • 15+ years of Life Science operational & engineering experience in the pharmaceutical, biotech or medical device sectors - Client side & Consulting experience highly preferred 

  • 10+ years’ experience with increasing responsibility in validation/quality service and project management of life sciences, biotech or other FDA regulated projects 

  • Diverse experience in leading CQV project teams related to the commissioning and qualification of clean utilities, facility systems, process support systems, bioprocess manufacturing systems, packaging equipment, and process and cleaning validation is desirable. 

  • Demonstrated client development experience and excellent presentation skills 

  • Experience with project management, good documentation practices, cGMP, & FDA validation methods and systems, ability to read engineering documents, set priorities, and work on multiple projects simultaneously.  

  • Experience building, managing, and leading teams 

  • Experience with creating proposals and business development. 

  • Experience with financial systems, project, and client administration 

  • Strong leadership, verbal communication, technical writing, project management tools and word processing skills. 

  • Working knowledge of process automation and computer system validation concepts, GAMP methodologies, 21 CFR Part 11 compliance and latest industry expectations for data integrity. 

  • Project Management experience in managing scope, cost, schedule, quality and risk is required. 

  • Excellent time management skills and ability to multi-task on simultaneous projects 

  • Travel as required for client development and project execution 

  • Displayed leadership in a consulting and service environment. 

  • Willing and able to travel as necessary for project requirements to include but not be limited to: project installation and start-up activities, client meetings, company sponsored meetings, trainings, industry related seminars, forums, or conventions, etc. 

  • BS Degree in Engineering or related technical degree  

   

  Our culture and commitment to our people is what sets us apart. We foster an environment of mutual respect, integrity, and unconditional interest in the individual and collective success of our professionals. Our model and entrepreneurial mindset offer a rewarding, challenging, and highly flexible path. Director of Compliance & Validation, Life Sciences, you will build a meaningful and fulfilling career with the support of professional development resources and mentorships including our First Year Experience program, Individual Development Plans, and Career Path resources and tools. You will be surrounded by exceptional talent who will support your development as both a world-class engineer and a highly effective leader.  LI-TH1
   
  Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments. 

 

At Barry-Wehmiller we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job.  If your experience is close to what you see listed here, please still consider applying.  We know that our differences often can bring about innovation, excellence and meaningful work—therefore, people from all backgrounds are encouraged to apply to our positions.  Please let us know if you require reasonable accommodations during the interview process. ​

Barry-Wehmiller is an equal opportunity employer. M/F/D/V This organization uses E-Verify.

 

Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.

 

Company:

Design Group