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Medtech Project Manager Jobs in Athens, GA (NOW HIRING)

Operational Excellence Technician

Athens, GA · On-site

$40K - $49K/yr

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... Applies project * management skills, tools, and techniques to manage the project and program scope ...

MedTech

Athens, GA · On-site

$37K - $46K/yr

Any other tasks, assignments, projects or requests as deemed by management. Qualifications * High School education preferred. * Must be 18 years of age or older. * Must read, write, speak and ...

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... A minimum of 3 years' experience with direct people management and/or project management experience ...

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... Demonstrated experience managing, organizing, planning, and coordinating projects * Demonstrated ...

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... Demonstrated experience managing, organizing, planning, and coordinating projects * Demonstrated ...

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... Work on other projects or assignments as requested by management. * Work rotating shifts including ...

Medtech Project Manager information

See Athens, GA salary details

$37.2K

$99.1K

$156.4K

How much do medtech project manager jobs pay per year?

As of Aug 11, 2026, the average yearly pay for medtech project manager in Athens, GA is $99,148.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,800.00 and $118,800.00 per year, depending on experience, location, and employer.

What does a Medtech project manager do?

A Medtech Project Manager oversees the planning, execution, and delivery of projects related to medical technology, such as the development of medical devices or healthcare software. They coordinate cross-functional teams, manage timelines and budgets, and ensure compliance with regulatory standards. Their role is crucial in bridging the gap between technical development, clinical requirements, and business goals to bring innovative medical solutions to market efficiently and safely.

What are the key skills and qualifications needed to thrive as a Medtech project manager?

To thrive as a Medtech Project Manager, you need a strong background in project management, biomedical engineering or life sciences, and a solid understanding of regulatory requirements, often supported by a relevant degree and PMP or similar certification. Familiarity with project management software like MS Project or Jira, as well as knowledge of FDA/CE regulations and quality management systems, is typically required. Exceptional leadership, communication, and problem-solving skills help drive cross-functional teams and manage stakeholder expectations. These abilities ensure timely product development, regulatory compliance, and successful project outcomes in the highly regulated Medtech industry.

How does a Medtech project manager typically collaborate with cross-functional teams during the product development lifecycle?

A Medtech Project Manager frequently works with cross-functional teams, including R&D, regulatory affairs, quality assurance, marketing, and manufacturing. They coordinate efforts by facilitating regular meetings, setting clear timelines, and ensuring all team members are aligned with project goals and compliance requirements. Strong communication skills are essential, as the Project Manager must translate technical updates between departments and resolve potential roadblocks promptly. This collaborative approach helps deliver innovative medical technologies efficiently while meeting regulatory standards.

What is the difference between Medtech Project Manager vs Medical Device Engineer?

AspectMedtech Project ManagerMedical Device Engineer
Required credentialsBachelor's in engineering, project management certification (PMP)Bachelor's or higher in biomedical, mechanical, or electrical engineering
Work environmentProject teams, cross-functional collaboration, client interactionsDesign, development, testing, and manufacturing of medical devices
Employer & industry usageMedical device companies, healthcare tech firmsMedical device manufacturing, R&D departments
Common search & comparison intentUnderstanding project management roles in medtechTechnical engineering roles in medical device development

The Medtech Project Manager focuses on overseeing medical device projects, coordinating teams, and ensuring timely delivery. In contrast, a Medical Device Engineer is primarily involved in designing, developing, and testing medical devices. Both roles require engineering backgrounds, but their daily tasks and responsibilities differ significantly, catering to different aspects of the medical device lifecycle.

What are popular job titles related to Medtech Project Manager jobs in Athens, GA? For Medtech Project Manager jobs in Athens, GA, the most frequently searched job titles are:
What job categories do people searching Medtech Project Manager jobs in Athens, GA look for? The top searched job categories for Medtech Project Manager jobs in Athens, GA are:
What cities near Athens, GA are hiring for Medtech Project Manager jobs? Cities near Athens, GA with the most Medtech Project Manager job openings:
Infographic showing various Medtech Project Manager job openings in Athens, GA as of June 2026, with employment types broken down into 38% Full Time, and 62% Part Time. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $99,148 per year, or $47.7 per hour.

Operational Excellence Technician

Johnson & Johnson

Athens, GA • On-site

$40K - $49K/yr

Full-time

Posted 11 days ago


Johnson & Johnson rating

8.3

Company rating: 8.3 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical


Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Supply Chain Manufacturing

Job Sub Function:

Manufacturing Process Improvement

Job Category:

Professional

All Job Posting Locations:

Athens, Georgia, United States of America, Cornelia, Georgia, United States of America

Job Description:

About MedTech

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.

We are searching for the best talent for Operational Excellence Technician

SECTION 1: JOB SUMMARY

  • Contributes as an entry to developing individual associate who works under close supervision.
  • Helps implement projects, programs, and processes in support of the organization's overall
  • Manufacturing Process Improvement strategy. Applies theoretical knowledge of the
  • Manufacturing Process Improvement field to carry out procedures and plans for the area.
  • Entry to developing individual contributor, who works under close supervision. Applies project
  • management skills, tools, and techniques to manage the project and program scope, quality,
  • schedule, budget, resources, and risk. Serves as primary contact for client and team queries
  • and concerns. Under the guidance of the Manufacturing Manager and/or Maintenance Manager,
  • the Operational Excellence Specialist supports the execution of site operational excellence
  • priorities by maintaining portfolio data integrity, coordinating purchasing activities, supporting
  • safety initiatives and programs, and facilitating continuous improvement efforts. The position
  • assists in tracking projects, CIPs, invoices, and key performance metrics to ensure alignment
  • with site goals and business objectives.

SECTION 2: DUTIES & RESPONSIBILITIES
In accordance with all applicable federal, state and local laws/regulations and CorporateJohnson & Johnson, procedures and guidelines, this position:
Helps execute programs and innovative initiatives for the Manufacturing ProcessImprovement area, under direct supervision.
Contributes to less complex components of projects, programs, or processes for the Manufacturing Process Improvement area.
Performs simple trend analyses to support continuous improvement of the organization's
Manufacturing Process Improvement strategy.
Documents the development of new manufacturing processes and improvements to existing
processes that maximize production capabilities and affordability.
Understands and applies Johnson & Johnson's Credo and Leadership Imperatives in dayto-day interactions with team.
This job does not require any experience. This job is overtime eligible.
Analyzes basic departmental expenditures and spend data to identify cost savingopportunities.
Support portfolio data integrity and data entry
Actively support safety initiatives and programs as per example good saves and safetyCAPAs
Assist in creating and tracking safety and housekeeping work orders.
Identifies and adheres to contract terms, compliance requirements and project management
methodologies for assigned projects.
Contributes to the implementation of systems that analyze, monitor, and track cost-spenddata, assess risk-benefit ratios, and provide insight on business impact.
Builds relationships with internal customers and works to identify their sourcing and projectmanagement needs.
Assists in the drafting of Requests for Proposals and quotes.
Carries out research pertaining to new project management tools and software that couldoptimize project management processes.
Identifies, maintains and monitors the Risks, Actions, Issues and Decisions (RAID) log.
Leads small kaizens with cross functional teams to assure causes of nonconformance are
identified and understood and that sound corrective/preventive actions are implemented.
Provides recommendations for the enhancement of processes and systems. Utilizesdocument change control system to update procedures and write protocols.
Implements corrections and process improvements.
Provides training and education to the manufacturing team(s) as needed
Acts in accordance with safety regulations and procedures.
Supports internal and external audits and inspections.
Comply with all job specific safety procedures and utilize PPE when necessary.
Comply with quality system requirements as defined within procedures and instructions.
Utilize applicable software systems as needed for the job (e.g. ComplianceWire, ADAPTIV,
etc.)
Consistently meet required work performance targets (RE's), if applicable
Support LEAN and Six Sigma Initiatives.
Support Maintenance Excellence (ME2) including 6S and Operator Asset Care.
Accurately complete records as defined within the job procedures (e.g. manual and/or
electronic documentation).
Consistently meet required Training due date targets.
Knowledge of processes and procedures within area of responsibility.
Maintains strong partnership with manufacturing, engineering, QA, and maintenance teams.
Willingness to travel to finishing plants if needed for investigations or for training as needed.
Follow current compliance regulations and standards
Responsible for communicating business related issues or opportunities to nextmanagement level
Responsible for following all Company guidelines related to Health, Safety andEnvironmental practices as applicable.
For those who supervise or manage a staff, responsible for ensuring that subordinatesfollow all Company guidelines related to Health, Safety and Environmental practices andthat all resources needed to do so are available and in good condition, if applicable
Responsible for ensuring personal and Company compliance with all Federal, State, localand Company regulations, policies, and procedures
Performs other duties assigned as needed

SECTION 3: EXPERIENCE AND EDUCATION

High school education or G.E.D. required.
Two-Year technical degree inSciences, Math,Applied ManufacturingTechnology, similar
related degree, equivalent formal training, or equivalent manufacturing experience related to
job requirements.
Experience in the QSR/ISO regulated medical device operation preferred.
Generally Requires 0-2 Years Work Experience

SECTION 4: REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSESand AFFILIATIONS
Strong computer skills and use of software application(s). Experience with Word and
Excel required. Experience with Minitab preferred.
Mechanical aptitude helpful.
Basic statistical and analytical problem- solving skills required; experience with
problem solving tools such as DMAIC, FishboneAnalysis, 5 Whys is preferred.
Proficient in the preparation of technical reports and presentations.
Strong communication and interpersonal skills.
Requires good networking and influencing skills.
Entails significant interaction with technical peers and manufacturing associates.
Self-motivated and capable of completing job duties with limited supervision.
Be able to work independently and in teams.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers. Internal employees contact AskGS to be directed to your accommodation resource.

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Required Skills:

Preferred Skills:


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