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Remote Fda Jobs in Gilbert, AZ (NOW HIRING)

System One

Senior Process Engineer

Tempe, AZ · Remote

$58 - $64/hr

Hybrid 4 days onsite, 1 day remote Overview Join a leading medical technology organization where ... Experience in an FDA regulated or regulated industry - preferred System One, and its subsidiaries ...

System One

Senior Process Engineer

Tempe, AZ · Remote

$58 - $64/hr

Hybrid 4 days onsite, 1 day remote Overview Join a leading medical technology organization where ... Experience in an FDA regulated or regulated industry - preferred System One, and its subsidiaries ...

Gateway Recruiting

TM

Phoenix, AZ · Remote

Adhere to FDA regulations, company policies, quality standards, and operating procedures ... Remote monitoring workflow development, Utilization ramp and adoption metrics * Strong executive ...

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See Gilbert, AZ salary details

$25.6K

$87.1K

$171.6K

How much do remote fda jobs pay per year?

As of Aug 8, 2026, the average yearly pay for remote fda in Gilbert, AZ is $87,145.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,630.00 and $113,057.00 per year, depending on experience, location, and employer.

What are the typical daily responsibilities of a remote FDA compliance specialist?

A Remote FDA Compliance Specialist generally reviews and updates regulatory documents, conducts virtual audits, and monitors company practices for FDA compliance. They regularly collaborate with cross-functional teams, such as quality assurance, legal, and product development, to provide guidance on regulatory requirements and respond to compliance queries. Additionally, they prepare and submit necessary reports, maintain records for inspections, and stay current on evolving regulations. This remote structure allows flexibility but also demands excellent organization, communication, and self-discipline to ensure all deadlines and compliance standards are met.

What is a remote FDA?

A Remote FDA job typically involves working for or with the U.S. Food and Drug Administration (FDA) from a remote location. These roles can include regulatory affairs, compliance, medical writing, research, and reviewing submissions for drug and medical device approvals. Remote FDA jobs require knowledge of FDA regulations, strong analytical skills, and experience in healthcare, pharmaceuticals, or related fields. They offer flexibility while maintaining high regulatory standards and ensuring public health and safety.

What are the key skills and qualifications needed to thrive in the remote FDA position, and why are they important?

To excel as a Remote FDA Compliance Specialist, you need in-depth knowledge of FDA regulations, quality assurance procedures, and a background in life sciences or a related field. Proficiency in using compliance management systems, electronic document management tools, and relevant certifications such as RAC (Regulatory Affairs Certification) are often required. Exceptional attention to detail, self-motivation, and strong written and verbal communication skills are vital for remote collaboration and thorough documentation. These abilities ensure regulatory adherence, minimize compliance risks, and facilitate effective remote teamwork within the pharmaceutical or medical device industry.

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Remote Fda jobs near you

Senior Process Engineer

System One

Tempe, AZ • Remote

$58 - $64/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 22 days ago

Job description

Job Title: Senior Process Engineer Location: Tempe, Arizona Type: Contract Compensation: $58- $64/hr Work Model: Hybrid 4 days onsite, 1 day remote

Overview Join a leading medical technology organization where you'll play a key role in bringing innovative products from development to manufacturing. This hybrid contract opportunity offers hands-on involvement with new product introductions, process validation, equipment implementation, and continuous improvement initiatives within a highly regulated environment. Ideal for engineers who enjoy collaborating across teams, driving process excellence, and making a direct impact on product quality and patient outcomes.

Responsibilities

  • Provide engineering support for new product and process introductions, ensuring activities are completed and documented in accordance with Stryker new product development procedures.
  • Ensure quality of process and product as defined in the appropriate operation and material specifications.
  • Assist in the selection and design of equipment based on analysis of specifications, reliability, and regulatory requirements.
  • Support capital acquisition activities, including specifying equipment, contract negotiation, installation, and validation.
  • Write operations manuals, troubleshooting manuals, continuous and preventive maintenance manuals.
  • Analyze equipment to establish operating data and conduct experimental test and result analysis.
  • Use engineering techniques to reduce product time to market while adhering to regulatory requirements, project deadlines, and product costs.
  • Participate in process review meetings.
  • Participate in process failure mode and effect analysis (PFMEA), control plan, standard operating procedures (SOP), and production part approval process (PPAP) generation associated with product transfers and launches.
  • Complete capability studies for in-process inspection and generate subsequent inspection documentation.
  • Conduct qualifications, validations, and measurement system analysis (MSA) studies for new products and new processes; review and approve validation documentation.
  • Work in a hands-on manner at the manufacturing site to support the implementation of new processes as specified in development.
  • Drive and execute effective communication with all stakeholders to enable project success.
  • Provide training for manufacturing team members.
  • Ensure adherence to GMP and safety procedures.
Requirements
  • 2+ years of relevant work experience – required
  • Bachelor’s degree in engineering – required
  • Bachelor's degree in Industrial or Systems Engineering – highly preferred
  • Lean Six Sigma Green Belt Certification or above – preferred
  • Knowledge of manufacturing processes, materials, product, and process design – preferred
  • Good understanding of design for manufacturing (DFM), related statistical tools, and validation/verification techniques – preferred
  • Experience writing and executing validations – preferred
  • Experience in new product introduction or manufacturing engineering – preferred
  • Experience in an FDA regulated or regulated industry – preferred

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Ref: #558-Scientific