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Remote Quality Engineer Medical Device Jobs in Georgia

Lead Substation Physical Engineer - REMOTE

Atlanta, GA · Remote

$98K - $129K/yr

Quality of life: Fully remote, flexible schedule, work-life balance * Investment of the community ... Leading the design and preparation of engineering studies such as: * AC Load * Illumination

Medical writing experience with US and EU regulatory requirements understanding in medical device ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

IT Testing Engineer II

Atlanta, GA · On-site +1

$70K - $90K/yr

Develop, update and maintain quality testing standards and procedures. * Follow standard testing ... medical condition, use of a guide dog or service animal, military/veteran status, citizenship ...

$73K - $174K/yr

Performance counters, Quality of Service (QoS) mechanisms, Techniques for Worst-Case Execution Time ... Device driver development experience * Linux operating system environment experience * Arm Based ...

We excel in IT consultative services and quality engineer development, with Good years of ... Support, even from afar, with our remote assistance. Regular salary reviews? You betcha! Ready to ...

Meticulous attention to detail and quality of work product * Ability to build and sustain ... medical device, or clinical * Experience leading validation deliverables for GxP systems, including ...

Meticulous attention to detail and quality of work product * Ability to build and sustain ... medical device, or clinical * Experience leading validation deliverables for GxP systems, including ...

Meticulous attention to detail and quality of work product * Ability to build and sustain ... medical device, or clinical * Experience leading validation deliverables for GxP systems, including ...

Remote Job Overview We are seeking experienced AI Consulting Domain Experts to contribute their ... Prompt Engineering * AI Output Evaluation * Quality Assurance * Technical & Report Writing

Showing results 41-60

Remote Quality Engineer Medical Device information

What does a remote quality engineer in the medical device industry do?

A Remote Quality Engineer in the medical device industry is responsible for ensuring that medical products meet regulatory and quality standards while working from a remote location. Their duties often include reviewing and improving quality processes, conducting audits, analyzing data to identify trends or issues, and ensuring compliance with regulations such as FDA or ISO 13485. They collaborate with cross-functional teams to resolve quality issues and may also be involved in risk management and validation activities. Remote Quality Engineers use digital tools to communicate and manage documentation, making it possible to fulfill their role away from a traditional office or manufacturing environment.

How does a remote quality engineer in the medical device industry effectively collaborate with cross-functional teams despite working off-site?

Remote Quality Engineers in the medical device sector regularly use digital collaboration tools such as video conferencing, shared documentation platforms, and cloud-based quality management systems to stay connected with design, manufacturing, and regulatory teams. While working remotely poses challenges in terms of immediate access to physical devices and face-to-face communication, frequent virtual meetings and clear documentation help ensure alignment on project goals and compliance requirements. Building strong relationships with on-site team members and proactively seeking feedback are key strategies for maintaining effective collaboration and ensuring product quality.

What are the key skills and qualifications needed to thrive as a remote quality engineer in medical devices, and why are they important?

To thrive as a Remote Quality Engineer in Medical Devices, you need a solid background in quality assurance, regulatory compliance (such as FDA and ISO 13485), and engineering principles, typically supported by a relevant engineering degree. Proficiency with quality management systems (QMS), document control software, and risk assessment tools is common, and certifications like ASQ CQE are highly valued. Strong attention to detail, effective problem-solving, and clear remote communication skills help ensure compliance and collaboration across distributed teams. These abilities are crucial for maintaining product safety, meeting regulatory standards, and driving continuous improvement in a regulated industry.

What are the most commonly searched types of Quality Engineer Medical Device jobs in Georgia?

The most popular types of Quality Engineer Medical Device jobs in Georgia are:

What are popular job titles related to Remote Quality Engineer Medical Device jobs in Georgia?

For Remote Quality Engineer Medical Device jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Remote Quality Engineer Medical Device jobs in Georgia look for?

The top searched job categories for Remote Quality Engineer Medical Device jobs in Georgia are:

What cities in Georgia are hiring for Remote Quality Engineer Medical Device jobs?

Cities in Georgia with the most Remote Quality Engineer Medical Device job openings:

Infographic showing various Remote Quality Engineer Medical Device job openings in Georgia as of August 2026, with employment types broken down into 73% Full Time, and 27% Contract. Highlights an 100% Remote job distribution.

Medical Science Liaison (MSL), CNS/Neuropsychiatry (Southeast)

TMAC

Atlanta, GA • Remote

Full-time

Re-posted 27 days ago


Job description

Medical Science Liaison (MSL), CNS/Neuropsychiatry (Southeast)

Territory: Northeast, 50-70% travel

Location: Home based anywhere in (GA, FL, NC, VA, TN, SC, KY, MS, AL)

Business Unit: Medical Affairs

Reports to: Senior Director, Field Clinical and Medical Programs, TMAC

SUMMARY

Serving as a field resource for the Company, the Medical Science Liaison (MSL) will support the company's neurology/psychiatry Phase II clinical development pipeline. The MSL will work full time to educate, analyze, and resolve issues with clinical research sites and investigators to support efforts to improve recruitment and activation timelines.

The MSL will be responsible for developing and fostering relationships with key stakeholders including clinical investigators and site staff to represent the company with the goal of improving enrollment, expanding current therapeutic concepts, and achieving enrollment and retention goals.

Duties and Responsibilities:

  • Strengthen the organization's scientific presence and credibility in neuropsychiatric disorders, including schizophrenia and bipolar depression
  • Maintain deep clinical and scientific expertise within the neuropsychiatric area
  • Partner with investigators and site staff to support clinical trials, ensuring understanding of protocols and patient requirements
  • Identify and recommend new clinical trial sites; support feasibility, site selection, and site initiation activities
  • Provide consistent, compliant scientific support to investigators and site personnel
  • Identify barriers to trial execution and contribute solutions to enhance recruitment and retention
  • Act as a field-based scientific resource, addressing trial-related questions and challenges
  • Build and maintain relationships with key opinion leaders (KOLs) and healthcare professionals
  • Collaborate cross-functionally with medical affairs, clinical development, and operations teams
  • Respond to unsolicited medical information requests in a compliant manner
  • Support scientific meetings, advisory boards, and conference activities

Qualifications:

  • Advanced degree (PharmD, PhD, MD, NP, PA) or equivalent terminal degree with appropriate clinical experience and scientific background preferred
  • 2+ years' CNS/Neuropsychiatry clinical, academic and/or medical experience required
  • Prior experience as an MSL (3-6 years); preferably with a clinical trial focus in a pre-launch setting required
  • Proven ability to engage Investigators/KOLs in non-promotional, scientific exchange
  • Ability to travel, locally and regionally, up to 50% with overnight stays (car, plane, train)
  • Knowledge of local regulatory requirements and Pharmaceutical Association Codes, including regulations governing compliant scientific exchange
  • Demonstrated ability to integrate and work in cross functional network/matrix
  • Demonstrated project management ability

The Medical Affairs Company (TMAC) has been the global provider of comprehensive clinical and medical staffing solutions for over 25 years. We specialize in the provision of field clinical and medical personnel based on our clients' distinct resources and lifecycle needs. Clients in the biopharmaceutical, diagnostics, and medical device fields have turned to us to help manage their short- and long-term strategic and tactical clinical trial and medical engagement goals, aimed at providing support to numerous stakeholders including physicians, site staff, community practitioners, caregivers, and patients.

Salary offers to be determined based on industry experience, education, and therapeutic expertise.

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