1970-01-01Davis Companieshttp://rev.daviscos.com/wp-content/themes/davis_theme/assets/images/logo.svgfull-time325 Donald J. Lynch Boulevard, Suite 201MarlboroughMA01752USAcustomer support[+800-482-9494][+508-481-8519]

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  • 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.
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Technical Coordinator

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    Technical Coordinator
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A fast-growing medical device company in the northern Twin Cities metro has an immediate opening on their team for a contract to hire Technical Coordinator! If you desire to step into the medical device world, this is the opportunity for you!

Responsibilities of the Technical Coordinator:

  • Create, Review, Track ECOs for R&D Audit/Maintain/Provide secure access to DHF
  • Maintain IBM Rational DOORS documents. Coordinate updates to department documents.
  • Create, Review, Track ECOs for R&D.
  • Audit/Maintain/Provide secure access to DHF.
  • Place documents in DHF / Provide a point person for secure DHF access.
  • Audit DHF throughout project for missing documents.
  • Work with appropriate functions to update FMEA, Standard Checklists, Product Specifications, Media Specs, Hazard Analysis documents and other department documents as necessary.
  • Conduct product release paperwork activities (PLR, NFG).
  • Organize R&D input to PLR forms, research and enter required information into form for product release.
  • Assist PM with NFG form, gain signatures on form. R&D coordinator for industry standards and Standards Assessment Checklist (SAC) process.
  • Update SAC SOP documents as standards change and new revisions are released.
  • Coordinate Part numbers, 21 level part releases, Article Quality Assessments, Label releases, Aspect/Impact. 

Qualifications of Technical Coordinator:
• AA or Trade Degree, or exhibited experience through past work history required, Bachelor’s degree preferred.

• Prefer minimum 3 years of experience in a Medical Device organization

• Prefer experience to be applicable to standard Document and Data control activities in a Quality System regulated environment.

• Knowledge of and ability to use personal computers to operate company systems e.g. Oracle, SharePoint, MS Word, Excel, Access, Project, Adobe Acrobat, IBM Rational DOORS, etc.

• Oracle experience desired and IBM Rational DOORS experience desired

• Knowledge of IEC 60601-1 series of medical device standards desired Abilities

DAVIS Companies partners with the top employers locally and nationally. They choose us because of our reputation for finding high quality talent, fast, but also our experience for evaluating and representing the best candidates in the marketplace.  We make every effort to provide updates and feedback to candidates at each stage of the process as we appreciate how stressful looking for a new role can be.  Apply today and experience “The DAVIS Difference”. 

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