Quality Engineer

1970-01-01Davis Companieshttp://daviscos.com/wp-content/themes/davis_theme/assets/images/logo.svg325 Donald J. Lynch Boulevard, Suite 201MarlboroughMA01752USAcustomer support[+800-482-9494][+508-481-8519]
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Quality Engineer

  • Specialty:

    Engineering
    • City:

      Franklin
    • State:

      MA
    • 02038
  • Assignment Type:

    Direct Hire
  • Job Id:

    52088

Description

We are looking for a Quality Engineer to join our client in Franklin, Ma on a direct hire baiss. 

The qualified candidate should be able to use Quality & Process Engineering principles, tools, and practices to develop and optimize systems and processes that are aligned with the overall business and quality vision of the company. 

Primary Responsibilities (Essential Functions):

  • The individual must be capable of working independently and in a team setting supporting the Quality and operations groups. Major responsibilities include:
  • Investigate and resolve work-in-process problems to reduce/eliminate scrap and rework
  • Analyze process statistics and conduct efficiency studies
  • Recommend and implement process improvements and modifications
  • Establish production/process standards
  • Implement real-time Statistical Process Control
  • Support on-site transfer projects and product scale-up activities.
  • Optimize manufacturing processes to provide sustainable gains in cost effectiveness and product performance through statistical analysis, designed experiments, and procedural changes.
  • Drive quality improvements by increasing internal competencies in process control/verification and validation studies, root cause analysis, failure mode and effect analysis (FMEA) and Process Excellence tools.
  • Work with suppliers, customers and participates in multi-functional teams to resolve technical/quality issues and develop new protocols.
  • Partner with Operations to assure alignment of goals, objectives and strategies.
  • Provide general engineering support to in-process inspection & incoming inspection.
  • Implement quality and efficiency improvements in in-process inspection.
  • Evaluates process critical quality parameters and updates specifications and protocols.
  • Additional duties and responsibilities as required.

Level of Skill, Education and Experience:

  • A minimum B.S. in an engineering discipline preferably mechanical engineering with 0-5 years of experience
  • Strong engineering skills, problem analysis/solving.
  • Excellent written and oral communication skills.
  • Understanding of GMP, FDA and SOP standards, guidelines and regulatory requirements.
  • Ability to work in a fast paced manufacturing environment while managing multiple projects.
  • Supplier quality experience highly desired.

Working knowledge of the following: 

  • Process validation and verification activities. (IQ, OQ, PQ, PPQ), risk analysis techniques, which include PFMEA (Process Failure Modes and Effects Analysis), Manufacturing Control Plans and Flow Plans, Blueprint & GD&T reading. 
  • Problem solving techniques including root cause analysis, and cause and effect analysis.
  • Proficiency with Microsoft Office products (Word, Excel, Project, PowerPoint) and Minitab.
  • Experience in medical device is highly desired.
  • Hands-on experience in the manufacturing, quality and process disciplines.

#MON

Quick Apply

  • As an Equal Employment Opportunity Employer, DAVIS has reporting requirements which require us to invite employees to voluntarily self-identify their race/ethnicity. Submission of this information is voluntary and refusal to provided it will not subject you to any adverse treatment. The information obtained will be kept confidential.
  • Accepted file types: pdf, doc, docx, txt, rtf.
  • By applying to this position and providing my contact information, I give The DAVIS Companies permission to provide me with email communications and information.

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