Sr. Quality Engineer
Beaver-Visitec International - Waltham, MA

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A Heritage of Precision, Innovation and Quality

Beaver-Visitec International is focused on developing and manufacturing new, innovative and reliable products for a variety of ophthalmic and specialty microsurgical procedures. Our products are distributed worldwide by sales and marketing professionals recognized throughout the industry for their clinical expertise and outstanding customer service. We have that “start-up” feel but have several well-established and recognized brands in our portfolio. We are continuously striving to improve our existing products while creating new, innovative products as technologies and market needs change.

We are currently seeking a Sr. Quality Engineer to join our quality and regulatory team. As a valued employee of Beaver-Visitec, you will enjoy a total benefits package including competitive salary, medical/dental/vision/life insurance, short- and long-term disability, fitness reimbursement, 401k, and more.



The Sr. Quality Engineer role is highly visible and challenging and you will often take a lead role in carrying out business/operating plans. You will be responsible for improving the effectiveness of the Quality System, supporting engineering and R&D projects, supporting operational/QA activities, preparing/reviewing/approving validation protocols and reports, and continuous improvement activities. You will often have a critical role in key project/initiative teams. Supervision of inspectors and technicians may be required. Your involvement in the business will make a significant impact on cost and productivity!



Required Skills and Knowledge:

B.S. degree in a Science or Engineering discipline with 5 or more years in a Quality Assurance Profession, or related position, in a manufacturing environment, and an in-depth knowledge of proven problem solving techniques such as Lean, DOEs, Statistical Analysis, TQMs, and Six Sigma. Experience leading and supporting teams, and cross training associates is a must for this position; Excellent written and verbal communication skills.

Preferred Skills and Knowledge:

Additional skills and knowledge that are valuable to the position include two years of experience with FDA QSR, and ISO13485 compliance.

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