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Medical Device Packaging Jobs in Powder Springs, GA

CorDx

Senior Production Manager

Atlanta, GA · On-site

Ensure manufacturing processes comply with ISO 13485 and regulatory requirements for medical device ... Highly competitive compensation package. * Comprehensive medical, dental, and vision insurance ...

CorDx

Senior Production Manager

Atlanta, GA · On-site

Ensure manufacturing processes comply with ISO 13485 and regulatory requirements for medical device ... Highly competitive compensation package. * Comprehensive medical, dental, and vision insurance ...

CorDx

Senior Production Manager

Atlanta, GA · On-site

Ensure manufacturing processes comply with ISO 13485 and regulatory requirements for medical device ... Highly competitive compensation package. * Comprehensive medical, dental, and vision insurance ...

Sotera Health

Operator

Atlanta, GA · On-site

$17 - $22.75/hr

... medical device companies and 9 of the top 10 pharmaceutical companies. Reporting to the Process ... package that includes: * Medical, Rx, Dental, Vision, Disability, Life Insurance, Health Savings ...

Spectrum Staffing Services

Be Seen First

Human Resources (HR) Coordinator

Powder Springs, GA · On-site

$55K - $60K/yr

BENEFITS * Competitive benefits package including medical, dental, and vision coverage ... Our Staffing Consultants are specialists in Human Resources, Scientific/Medical Device, Engineering ...

ICON

Senior Clinical Research Associate

Atlanta, GA · On-site +1

The ideal candidate will have cardiovascular medical device monitoring experience- however, complex ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

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All JobsMedical Device Packaging JobsMedical Device Packaging Jobs in Powder Springs, GA

Medical Device Packaging information

See Powder Springs, GA salary details

$10

$16

$19

How much do medical device packaging jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for medical device packaging in Powder Springs, GA is $16.05, according to ZipRecruiter salary data. Most workers in this role earn between $13.65 and $16.83 per hour, depending on experience, location, and employer.

What is a medical device packaging?

A Medical Device Packaging job involves designing, testing, and ensuring that medical devices are packaged safely and in compliance with regulatory standards. Professionals in this field work to protect devices from contamination, damage, and environmental factors during storage and transportation. They collaborate with engineers, quality assurance teams, and regulatory experts to develop packaging solutions that meet industry regulations like ISO 11607 and FDA guidelines. This role also includes conducting validation testing, documenting processes, and improving packaging efficiency.

What does a typical day look like for someone working in medical device packaging?

A typical day in Medical Device Packaging involves preparing and inspecting medical devices for packaging, ensuring materials and labels comply with regulatory standards, and maintaining accurate documentation. You’ll work closely with production teams, quality assurance staff, and sometimes engineers to troubleshoot issues and improve processes. The role requires handling packaging equipment, performing visual inspections, and following detailed protocols to minimize contamination risks. Collaboration and communication with other departments are frequent, making teamwork a key part of daily responsibilities.

What are the key skills and qualifications needed to thrive in medical device packaging, and why are they important?

To thrive in Medical Device Packaging, you need attention to detail, knowledge of packaging materials and regulations, and often a background in manufacturing or life sciences. Familiarity with quality assurance systems, Good Manufacturing Practices (GMP), and labeling software or validation equipment is important. Strong organizational skills, teamwork, and the ability to follow precise instructions help ensure high standards are consistently met. These skills are critical because packaging must protect devices, comply with regulatory standards, and ensure patient safety.

What cities near Powder Springs, GA are hiring for Medical Device Packaging jobs?

Cities near Powder Springs, GA with the most Medical Device Packaging job openings:

Medical Device Packaging jobs near you
Infographic showing various Medical Device Packaging job openings in Powder Springs, GA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $33,387 per year, or $16.1 per hour.

Senior Regulatory Affairs Manager (Onsite)

CorDx

Atlanta, GA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 5 days ago

Job description

Who is CorDx?
CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.
Job Type: Full time
Job Title: Senior Regulatory Affairs Manager
Location: Onsite - Atlanta, or San Diego
Position Summary:
The Senior Regulatory Affairs Manager will play a crucial role in leading and managing the regulatory submissions for CorDx medical device products, including 510(k) and submissions. This individual will ensure compliance with all applicable regulations in the preparation of the submissions to FDA, provide regulatory guidance to cross-functional teams, and contribute to the successful approval and launch of innovative medical devices.
Key Responsibilities:
  • Prepare, review, and submit regulatory documents to FDA.
  • Manage and oversee the regulatory submission process, ensuring timely and successful clearances/approvals.
  • Ensure that all products comply with applicable regulatory requirements, including FDA regulations and ISO standards.
  • Provide regulatory guidance to R&D team during product development life cycle.
  • Stay updated on changes in regulatory requirements and communicate potential impacts to the organization.
  • Conduct regulatory assessments for product changes and provide recommendations for appropriate regulatory pathways.
  • Collaborate with internal stakeholders and external partners to ensure alignment on regulatory strategies and project timelines.
  • Represent the company in meetings with regulatory agencies and external partners as needed.
  • Ensure proper documentation and maintenance of regulatory submissions and correspondence with regulatory agencies.

Requirements
  • Master's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field; advanced degree preferred.
  • Minimum of 7-10 years of experience in regulatory affairs within the medical device industry.
  • Proven track record of leading and successfully obtaining 510(k) and clearances/approvals.
  • Experience in interacting with FDA and other regulatory agencies.

Skills & Competencies:
  • In-depth knowledge of FDA regulations, 21 CFR Part 820, ISO 13485, and other applicable medical device regulations.
  • Strong leadership and project management skills, with the ability to manage multiple projects and priorities.
  • Excellent communication, negotiation, and problem-solving skills.
  • Ability to work collaboratively in a cross-functional team environment.
  • Detail-oriented with strong organizational skills.

Benefits
  • Highly competitive compensation package.
  • Comprehensive medical, dental, and vision insurance.
  • 401(k) plan with generous company contributions.
  • Flexible paid time off (PTO) policy.
  • Additional substantial benefits.

Equal Opportunity Statement: We are an equal opportunity employer committed to inclusion and diversity. We do not discriminate based on race, gender, religion, sexual orientation, age, color, marital status, veteran status, disability status, national origin, or any other protected characteristic.

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