Senior Quality Engineer

Barry-Wehmiller • Boston, MA

23d

About The Position

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: Sr. Quality Engineer Who You’ll Work With You will join one of our 45 offices in the US, be part of a committed team of over 1500 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 Design Group as a Sr. Quality Engineer , 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 expert s 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 client s . Together, you will help our clients make critical changes to improve their performance and realize their most important goals. Responsible for day-to-day communication, coordination, and organization of onsite project execution activities. Provide leadership and mentorship to other professionals. Provide customized Quality solutions to clients with challenging and unique needs. Provide direction and guidance to clients and other professionals with regards to Quality Systems, Change Management, Investigations, and/or Process Improvement initiatives as defined by DG’s clients. Provide review and comments to other professionals regarding Quality impacting deliverables. All Design Group Project Managers have leadership skills and experience in Life Science Project Management and have a drive and desire to grow and expand local and regional clients. Make an impact day-to-day with your skills and expertise , strengthening that relationship with our clients and team What You’ll Bring Minimum 10 years of quality engineering or management experience. Must have experience managing and maintaining schedules and coordinating professionals. Must have experience developing Project Plans and Execution Strategies. Must have experience leading investigations and troubleshooting issues. Must have strong computer, written, and verbal communication skills. Understanding and experience with Validation activities is preferable. Pharmaceutical, Biotech and/or Medical Device project experience is . Strong knowledge of FDA requirements, cGMPs , and standard QMS procedures is . 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, compa ny sponsored meetings, training s, industry related seminars, forums, or conventions, etc. B.S. in Engineering, Chemistry, Microbiology, or related technical degree. Equivalent years of experience in as a Project Manager or Quality Engineer can be substituted for 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. As a Sr. Quality Engineer , you will build a meaningful and fulfilling career with the support of professional development resources and mentors hips 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 . Feel like you're on the path to becoming a Sr. Quality Engineer but you're not quite there yet? We'd love to connect with you to see if we can take you from where you are today and grow you into a Design Group Engineering Consultant. 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

Requirements

• Minimum 10 years of quality engineering or management experience.
• Must have experience managing and maintaining schedules and coordinating professionals.
• Must have experience developing Project Plans and Execution Strategies.
• Must have experience leading investigations and troubleshooting issues.
• Must have strong computer, written, and verbal communication skills.
• Strong knowledge of FDA requirements, cGMPs , and standard QMS procedures is .
• 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, compa ny sponsored meetings, training s, industry related seminars, forums, or conventions, etc.
• B.S. in Engineering, Chemistry, Microbiology, or related technical degree.
• Equivalent years of experience in as a Project Manager or Quality Engineer can be substituted for degree .

Nice To Haves

• Understanding and experience with Validation activities is preferable.
• Pharmaceutical, Biotech and/or Medical Device project experience is .

Responsibilities

• Responsible for day-to-day communication, coordination, and organization of onsite project execution activities.
• Provide leadership and mentorship to other professionals.
• Provide customized Quality solutions to clients with challenging and unique needs.
• Provide direction and guidance to clients and other professionals with regards to Quality Systems, Change Management, Investigations, and/or Process Improvement initiatives as defined by DG’s clients.
• Provide review and comments to other professionals regarding Quality impacting deliverables.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees