Quality Engineer at Design Group
Boston, MA 02116, USA -
Full Time


Start Date

Immediate

Expiry Date

09 Sep, 25

Salary

0.0

Posted On

10 Jun, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Conventions, Manufacturing, Calibration, Life Sciences, Iso, Change Control, Documentation Practices, Microbiology, Testing, Medical Devices, Chemistry, Technical Writing, Maintenance

Industry

Mechanical or Industrial Engineering

Description

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:


  • Quality Engineer

Feel like you’re on the path to becoming a 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.

  • Additional Job Description
  • Plans and directs activities concerned with development, application, and maintenance of quality standards for industrial processes, materials and products
  • Engages in quality control processes or procedures including product inspection, testing and analysis of products, reporting on quality to management, and approving or denying product release
  • Establishes programs to evaluate precision and accuracy of equipmentOther duties as assigne
Responsibilities

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.

  • Ensure that processes adhere to quality standards during all phases of production:
  • Draft standard operating procedures, work instructions, and inspection, evaluation, and testing methods
  • Execute field test protocols including IQ, OQ, PQ, and PV
  • Identify, interface, and operate medical devices
  • Make an impact day-to-day with your skills and expertise, strengthening that relationship with our clients and team

What You’ll Bring :

  • A minimum of 3 years of experience in life sciences, medical devices, or other FDA regulated environments, preferably in ISO 13485 or ISO 9001
  • Experience drafting standard operating procedures and methods for inspection, testing, and evaluation
  • Experience working with QSR systems including calibration, maintenance, CAPA, and non-conformances
  • Experience utilizing change control, risk management, and mitigation tools (PFMEA/DFMEA)
  • Experience authoring and executing systems qualifications (IQ/OQ/PQ) for clean utilities, facilities, manufacturing, and packaging equipment (preferred)
  • Experience with good documentation practices, cGMP, and FDA validation methods and systems
  • The ability to read engineering documents, set priorities, and work on multiple projects simultaneously
  • Strong verbal communication, technical writing, and word processing skills
  • A willingness to travel for project requirements including installation and start-up activities, client and company sponsored meetings, trainings, industry related seminars, forums, and conventions
  • A bachelor of science in engineering, chemistry, microbiology, or a related technical degree, or equivalent experience as a project manager or quality engineer

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 Quality Engineer, 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.

Feel like you’re on the path to becoming a 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.

  • Additional Job Description
  • Plans and directs activities concerned with development, application, and maintenance of quality standards for industrial processes, materials and products
  • Engages in quality control processes or procedures including product inspection, testing and analysis of products, reporting on quality to management, and approving or denying product release
  • Establishes programs to evaluate precision and accuracy of equipmentOther duties as assigned

  • 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.

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