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Service Manager Medical Devices Jobs (NOW HIRING)

Arthrex

Technician II - Medical Devices

Santa Barbara, CA · On-site

$23 - $37.75/hr

Technician II - Medical Devices Salary Range: Salary Minimum: $23.00/hr Salary Maximum: $37.75/hr ... Ability to communicate ideas and issues effectively to other team members and management. Knowledge:

SandboxAQ

$77K - $105K/yr

Senior Platform Engineer, Medical Devices Location United States Employment Type Full time Location ... The company's Large Quantitative Models (LQMs) power advances in life sciences, financial services ...

Apple

Senior Lead Auditor (Medical Devices)

Cupertino, CA · On-site

$149K - $249K/yr

Every new product we build, service we create, or Apple Store experience we deliver is the result ... management system audit processes Independently supports internal audit program. Generates and ...

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How much do service manager medical devices jobs pay per year?

As of Sep 10, 2026, the average yearly pay for service manager medical devices in the United States is $69,971.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,000.00 and $80,500.00 per year, depending on experience, location, and employer.

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Senior Manager Regulatory Affairs - Medical Devices

Covington, GA • On-site

Intermedia Group Inc.
See more jobs at Intermedia Group Inc.external

$150K - $165K/yr

Other

Posted 7 days ago

Job description

Senior Manager Regulatory Affairs – Medical Devices
  • Covington, GA
  • $150,000 to $165,000

OPEN JOB: Senior Manager Regulatory Affairs – Medical Devices

LOCATION: Covington, Georgia

***Relocation Assistance Available

***WFH on Fridays

BASE SALARY: $150,000 to $165,000

INDUSTRY: Medical Equipment / Devices

Responsibilities

  • Develop and implement comprehensive regulatory strategies for new product development, product
  • life cycle management, and post-market surveillance activities.
  • Prepare, review, and submit regulatory documents, including 510(k)s, Dossiers, Technical Files, and other international submissions to global health authorities.
  • Act as the primary regulatory contact for assigned projects, communicating directly with regulatory agencies during submissions, reviews, and inspections.
  • Interpret and apply complex regulations, guidance documents, and industry standards to ensure product compliance throughout the development and commercialization process.
  • Lead and mentor junior regulatory affairs professionals, fostering a culture of compliance and continuous improvement.
  • Participate in internal and external audits, providing regulatory expertise and support.
  • Assess the regulatory impact of product changes, manufacturing changes, and quality system changes.
  • Collaborate effectively with R&D, Quality, Clinical, Marketing, and other relevant departments to achieve regulatory objectives.
  • Monitor and disseminate information regarding new or changing regulatory requirements and industry trends relevant to the company's product portfolio.

Job Qualifications

  • Bachelor's degree in a scientific or technical discipline (e.g., Biomedical Engineering, Chemistry, Biology) required. Advanced degree (MS, PhD) preferred.
  • Minimum of 8-10 years of experience in Regulatory Affairs within the medical device industry, with at least 3-5 years in a leadership or senior role.
  • Demonstrated expertise in preparing and submitting various regulatory applications (e.g., 510(k), PMA, CE Mark, International registrations).
  • Strong knowledge of FDA regulations (21 CFR Parts 800s), ISO 13485, Medical Device Regulation (EU MDR), and other relevant international regulatory requirements.
  • Excellent written and verbal communication skills, with the ability to effectively communicate complex regulatory information to diverse audiences.
  • Proven ability to lead projects, manage multiple priorities, and work effectively in a fast-paced environment.
  • RAC (Regulatory Affairs Certification) preferred.
  • Proficiency in regulatory information management systems and tools.
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