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Quality Assurance Specialist

Full Time
full time
UNAVAILABLE
4 Nov 2025
Somerville
Verified by Turrior

Content + Source + Freshness • 17 Dec 2025 • 95% confidence

78 / 100

Offer value

A solid offering for those with QA experience in regulated industries, though salary details are vague which slightly lowers the score.

  • Solid role in the healthcare tech sector
  • Comprehensive QA responsibilities with room for collaboration
  • Remote work options offering better work-life balance
Pros
  • Opportunity to work in a crucial sector (health tech) with compliance standards
  • Scope for cross-functional collaboration and potential for impacting products
  • Remote working environment enhances work-life balance
Cons
  • Lack of detailed salary information could deter candidates
  • Requires specialized knowledge which may limit applicant pool
  • Limited information on career advancement opportunities

Who it's for

Mid-level • Remote

Good fit
  • Mid-level QA professionals with regulatory backgrounds
  • Individuals passionate about healthcare product quality
  • Candidates seeking remote work flexibility
Not recommended for
  • Entry-level QA candidates
  • Those without interest in regulated industries
  • Applicants who need clear salary details upfront

Motivation fit

Interest in enhancing product quality in health techDesire to develop skills in effective QA processes and regulationsMotivation to work in cross-industry teams

Key skills

Quality assurance in regulated environmentsFamiliarity with QMS processesProject lifecycle managementTeam collaboration and mentorship
Score: 78/100 AI verified analysis

About the job

Responsibilities

Job Title: Quality Assurance Specialist - US 

Reports to: Head of Quality & Regulatory

FLSA Status: Exempt

 

Job Summary

The Quality Assurance Principal is responsible for supporting DeepHealth products and product development, along with the Quality Management System throughout the organization.  The Quality Assurance Principal will be responsible for collaborating cross-functionally to support and guide product development. The Quality Assurance Principal will work cross-functionally and within the team to support the Quality processes, such as QMS training, complaint and CAPA management. 

 

Essential Duties and Responsibilities 

 

As the Quality Assurance Principal, this position will: 

  • Actively engage cross-functionally within the organization, such as with the Engineering, Clinical and Marketing teams, to develop new products within the Product Lifecycle Management (PLM) and New Product Introduction (NPI) processes. 
  • Act as the Quality lead for design changes to existing DeepHealth products, including non-medical devices, to ensure compliance with the applicable standards and guidances. 
  • Guide junior Quality Assurance team members to ensure consistent implementation of Quality processes, including design control and risk management. 
  • Take ownership of product specific Quality Management System processes, such as CAPAs and complaint management, across the organization to ensure compliance and drive efficiency.   
  • Work cross-functionally to integrate products as a result of corporate and/or product acquisitions. 
  • Work as a team member with the Quality Assurance team to ensure compliance to US and OUS standards and regulations. 
  • Participate in the development of junior staff, as requested 
  • Collect/monitor quality metrics in support of Management Review 

 

 

PLEASE NOTE: This is not an exhaustive list of all duties, responsibilities and requirements of the position described above.  Other functions may be assigned and management retains the right to add or change duties at any time.

 

Minimum Qualifications, Education and Experience

  • Bachelor’s degree in relevant field (or equivalent experience, i.e. Associate’s degree with 5 years of experience). 
  • Minimum of -10 working in a regulated industry (FDA and Software as a Medical Device preferred). 
  • Strong knowledge of FDA Quality System Regulations, including but not limited to, 21 CFR 11, and 21 CFR 820. 
  • Knowledge of EU Medical Device Regulation (MDR), ISO13485, ISO 14971, and IEC 62304 preferred. 
  • Knowledge and understanding of pre- and post- market clinical studies, including but not limited to, 21 CFR 812, 21 CFR 50, and 21 CFR 56, preferred but not required. 
  • Participation in regulatory audits a plus 
  • Excellent written and oral communication skills 

 

 

Physical Demands

This position often requires sitting, standing, walking, bending, twisting, reaching with hands and arms, using hands and fingers, handling, or feeling, speaking, listening, and high-level cognitive thinking. Also, must be able to lift up to 10 pounds occasionally. The position requires the ability to travel (~10% of time), drive a vehicle, and utilize other forms of transportation. 

 

Working Environment

Remote. This position requires domestic / international travel up to 15%.

 

ACCOMMODATIONS
Reasonable accommodations may be made to enable people with disabilities to perform the essential functions of the job.

 

 

 

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