Document Control Specialist – Medical Devices & eQMS
BrioHealth Solutions
Burlington (VT)
On-site
USD 80,000 - 100,000
Full time
14 days+
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Benefits offered by this job
Medical insurance
Vision insurance
401(k)
Paid maternity leave
Paid paternity leave
Job summary
A Med-Tech Company is seeking a detail-oriented Document Control Specialist in Burlington, MA to ensure compliance with FDA regulations. Responsibilities include managing the electronic Quality Management System, supporting employee training, and overseeing document control processes. Ideal candidates will have 2-4 years of experience in configuration management and strong communication skills. This is a full-time, onsite role with minimal travel.
Qualifications
2-4 years of configuration management experience in the medical device industry.
Exceptional attention to detail and critical thinking skills.
Effective communication skills with stakeholders.
Responsibilities
Co-administer the electronic Quality Management System (eQMS).
Support onboarding and training of new employees.
Review change control packets for compliance.
Skills
Attention to detail
Critical thinking
Organizational skills
Effective communication
Multitasking
Education
Associate's or Bachelor's degree in STEM or Life Sciences
Job description
A Med-Tech Company is seeking a detail-oriented Document Control Specialist in Burlington, MA to ensure compliance with FDA regulations. Responsibilities include managing the electronic Quality Management System, supporting employee training, and overseeing document control processes. Ideal candidates will have 2-4 years of experience in configuration management and strong communication skills. This is a full-time, onsite role with minimal travel.