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Manager Medical Device Operations Jobs in Decatur, GA

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Medical Device Sales Representative Territory: Southeastern states Employment Type: Full-Time ... CRM systems * Collaborate with marketing, clinical, and operations teams to support product ...

Devops Engineer

Atlanta, GA · On-site

$50.75 - $69.50/hr

Role Overview We are seeking a AWS Operations Specialist to manage and maintain our cloud infrastructure and device ecosystems. This is a highly operational, execution-focused role-not an ...

... care medical device solutions used in the detection of infectious diseases such as COVID-19 ... Key Responsibilities: Operations Management * Oversee all day-to-day operations, including ...

... care medical device solutions used in the detection of infectious diseases such as COVID-19 ... Key Responsibilities: Operations Management * Oversee all day-to-day operations, including ...

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Manager Medical Device Operations information

See Decatur, GA salary details

$30.3K

$62K

$115.7K

How much do manager medical device operations jobs pay per year?

As of Sep 3, 2026, the average yearly pay for manager medical device operations in Decatur, GA is $61,954.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,000.00 and $75,700.00 per year, depending on experience, location, and employer.

What is a manager medical device operations?

A Manager Medical Device Operations oversees the daily activities and processes involved in manufacturing, distributing, and maintaining medical devices. They ensure that operations comply with regulatory standards, manage teams, and work to optimize efficiency, quality, and safety. This role often involves coordinating with other departments, handling audits, and implementing process improvements to meet organizational goals. They play a critical role in ensuring that medical devices reach healthcare providers and patients safely and on time.

What are the key skills and qualifications needed to thrive as a manager medical device operations?

To excel as a Manager Medical Device Operations, you need expertise in supply chain management, regulatory compliance (such as FDA and ISO standards), and operational leadership, typically supported by a bachelor’s degree in engineering, life sciences, or business. Familiarity with ERP systems, quality management software, and relevant certifications like Six Sigma or PMP are commonly required. Strong communication, problem-solving, and team leadership skills help drive cross-functional collaboration and continuous improvement. These competencies are essential for ensuring product quality, regulatory adherence, and efficient operations in a highly regulated industry.

What are some common challenges faced by a manager medical device operations, and how can they be addressed?

Managers in Medical Device Operations often face challenges such as ensuring compliance with strict regulatory standards, coordinating cross-functional teams, and managing supply chain complexities. Staying proactive with regulatory updates, fostering open communication among departments, and implementing robust quality management systems can help address these issues. Additionally, investing in staff training and process improvement initiatives can streamline operations and minimize delays or compliance risks.

What are popular job titles related to Manager Medical Device Operations jobs in Decatur, GA?

For Manager Medical Device Operations jobs in Decatur, GA, the most frequently searched job titles are:

What job categories do people searching Manager Medical Device Operations jobs in Decatur, GA look for?

The top searched job categories for Manager Medical Device Operations jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Manager Medical Device Operations jobs?

Cities near Decatur, GA with the most Manager Medical Device Operations job openings:

Infographic showing various Manager Medical Device Operations job openings in Decatur, GA as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 17% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $61,954 per year, or $29.8 per hour.

Medical Device Quality Systems & FDA Inspection Readiness Consultant

The FDA Group

Atlanta, GA

Full-time

Posted 7 days ago


Job description

Medical Device Quality Systems & FDA Inspection Readiness Consultant

Location: Atlanta/Duluth, Georgia area
Work Arrangement: Onsite
Duration: Immediate start through November 2026, with potential extension
Start: Immediate

Position Overview

We are seeking an experienced Medical Device Quality Systems Consultant to provide hands-on support for the startup of a new Class I medical device contract manufacturing operation.

The consultant will support Quality Management System (QMS) implementation, development of auditable quality and operational processes, system validation, and FDA inspection readiness. A key focus will be ensuring appropriate controls are established across production, warehousing, inventory, traceability, product hold/quarantine, release, and direct-to-consumer distribution activities.

The engagement will require both quality systems expertise and practical implementation support as the organization works toward regulatory and operational milestones in October and a planned November 1 go-live. The consultant may also provide training and ongoing Quality support following launch.

Key Responsibilities

  • Review the existing QMS and tailor requirements and processes for the new medical device manufacturing operation.

  • Support implementation of the QMS and ensure processes are operational, documented, and auditable.

  • Develop new quality and operational processes needed to support manufacturing and distribution activities.

  • Support validation of the warehouse management system and associated workflows.

  • Establish and/or assess controls for production, inventory management, product traceability, quarantine/hold, and product release.

  • Develop appropriate quality checks and controls for direct-to-consumer product shipments.

  • Assess Quality System and operational readiness for an anticipated FDA inspection.

  • Identify inspection-readiness gaps and support implementation of corrective actions before go-live.

  • Work directly with facility personnel to operationalize new procedures and quality controls.

  • Provide employee training and implementation support for new or revised processes, as needed.

  • Support the organization through its planned November 1 launch and provide ongoing Quality support following go-live, as needed.

Required Qualifications

  • Significant medical device Quality or Quality Systems experience.

  • Demonstrated experience implementing or adapting a QMS for medical device operations.

  • Strong knowledge of FDA medical device quality requirements and inspection readiness.

  • Experience developing and implementing auditable quality and operational processes.

  • Experience with warehouse, distribution, inventory, traceability, quarantine/hold, and product release controls.

  • Experience supporting computerized system validation or validation of warehouse/inventory management systems.

  • Ability to provide hands-on implementation support and work directly with site personnel.

  • Ability to work onsite in the Atlanta/Duluth, Georgia area.

Preferred Qualifications

  • Experience supporting startup or launch activities for a medical device manufacturing operation.

  • Experience with Class I medical devices.

  • Experience establishing quality controls for direct-to-consumer distribution.

  • Local to the Atlanta/Duluth, Georgia area.

Work Arrangement

This engagement requires onsite support in the Atlanta/Duluth, Georgia area. Local consultants are preferred to facilitate consistent onsite support.

Ideal Candidate

The ideal consultant is a hands-on Medical Device Quality Systems professional with experience taking QMS requirements from documented procedures through practical implementation. The consultant should be comfortable working across quality systems, warehouse and distribution controls, system validation, and FDA inspection readiness while helping a new manufacturing operation prepare for launch.