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Medical Device Packaging Jobs in Edison, NJ (NOW HIRING)

Strive Pharmaceuticals Inc.

Be Seen First

Warehouse Inventory Specialist

Cranbury, NJ · On-site

$22/hr

Experience in pharmaceutical or medical device packaging environment * Familiarity with lot traceability, batch records, and audit processes * Forklift certification or material handling equipment ...

Strive Pharmaceuticals Inc.

Be Seen First

Warehouse Inventory Specialist

Cranbury, NJ · On-site

$22/hr

Experience in pharmaceutical or medical device packaging environment * Familiarity with lot traceability, batch records, and audit processes * Forklift certification or material handling equipment ...

Ro

Packaging Program Manager

New York, NY · On-site +1

$122K - $140K/yr

Experience working with packaging, product commercialization, manufacturing, pharmaceutical, medical device, or consumer products is required * Proven ability to manage multiple complex initiatives ...

Ro

Packaging Program Manager

New York, NY · On-site +1

$122K - $140K/yr

Experience working with packaging, product commercialization, manufacturing, pharmaceutical, medical device, or consumer products is required * Proven ability to manage multiple complex initiatives ...

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All JobsMedical Device Packaging JobsMedical Device Packaging Jobs in Edison, NJ

Medical Device Packaging information

See Edison, NJ salary details

$11

$17

$21

How much do medical device packaging jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for medical device packaging in Edison, NJ is $17.55, according to ZipRecruiter salary data. Most workers in this role earn between $14.95 and $18.41 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 are popular job titles related to Medical Device Packaging jobs in Edison, NJ?

For Medical Device Packaging jobs in Edison, NJ, the most frequently searched job titles are:

What job categories do people searching Medical Device Packaging jobs in Edison, NJ look for?

The top searched job categories for Medical Device Packaging jobs in Edison, NJ are:

What cities near Edison, NJ are hiring for Medical Device Packaging jobs?

Cities near Edison, NJ with the most Medical Device Packaging job openings:

Medical Device Packaging jobs near you
Infographic showing various Medical Device Packaging job openings in Edison, NJ 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, 2% Hybrid, and 6% Remote job distribution, with an average salary of $36,502 per year, or $17.5 per hour.

Staff Engineer, R&D Packaging - Wayne, NJ

Getinge

Wayne, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 25 days ago

Getinge rating

9.3

Company rating: 9.3 out of 10

Based on 14 frontline employees who took The Breakroom Quiz

13th of 499 rated machine equipment manufacturers

Job description

With a passion for life
Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.
Are you looking for an inspiring career? You just found it.
Job Overview
This position serves as a technical leader and subject matter expert for packaging systems, labeling, and sterile barrier solutions supporting Cardiac Surgery and Vascular Intervention product portfolios. This role drives the development, validation, commercialization, lifecycle management, and continuous improvement of complex packaging systems while ensuring compliance with global regulatory requirements.
The Staff Packaging Engineer provides strategic technical leadership across multiple programs, mentors engineers, influences packaging standards and best practices, partners with cross-functional stakeholders, and leads initiatives that improve product quality, patient safety, manufacturing efficiency, supply continuity, and total cost of ownership
Job Responsibilities and Essential Duties
Technical Leadership
  • Serve as the packaging engineering subject matter expert (SME) for sterile and non-sterile medical device packaging systems.
  • Lead packaging strategy, design, development, validation, and commercialization activities for new product development and sustaining engineering projects.
  • Establish technical direction for packaging technologies, materials, validation methodologies, and packaging standards.
  • Drive innovation and continuous improvement initiatives focused on quality, reliability, sustainability, manufacturability, and cost optimization.
  • Mentor and provide technical guidance to packaging engineers and cross-functional project teams.

Packaging Development
  • Lead the design and development of sterile barrier systems and protective packaging solutions in compliance with ISO 11607 and applicable global regulations.
  • Evaluate and select packaging materials based on product requirements, sterilization compatibility, transportation risks, shelf-life requirements, and environmental considerations.
  • Guide packaging architecture decisions across product platforms and manufacturing sites.
  • Lead packaging component specifications, drawings, and technical documentation development.
  • Support platform standardization and harmonization initiatives across the portfolio.

Validation and Compliance
  • Develop and approve validation strategies and protocols including: IQ, OQ, PQ, Process validation, Packaging validation, Package integrity testing, Transportation simulation testing, Accelerated and real-time aging studies, and Labeling system validation
  • Lead risk assessments utilizing Design Failure Mode and Effects Analysis (DFMEA), Process FMEA, and hazard analysis methodologies.
  • Ensure compliance with ISO 11607, ISO 13485, FDA 21 CFR Part 820, EU MDR, UDI requirements and Global medical device regulations

Manufacturing and Operations Support
  • Partner with Manufacturing, Quality, Regulatory Affairs, Supply Chain, and Operations teams to implement robust packaging solutions.
  • Lead resolution of packaging-related manufacturing issues and non-conformances.
  • Support investigations, CAPAs, complaint trending, and quality system activities.
  • Drive process capability improvements through statistical analysis and data-driven decision-making.
  • Lead supplier qualification activities and packaging component change management.

Strategic and Business Impact
  • Lead cross-functional projects with significant business, technical, and regulatory complexity.
  • Identify and execute cost reduction opportunities through packaging redesign, material optimization, and supplier management.
  • Support business continuity initiatives related to packaging materials and suppliers.
  • Influence organizational packaging standards, engineering practices, and technology roadmaps.
  • Present technical recommendations and project updates to senior leadership.

Minimum Requirements
  • Bachelor's degree in Packaging Engineering, Mechanical Engineering, Biomedical Engineering, Materials Science, or related technical discipline. Master's degree in Engineering, Packaging Engineering, or related discipline (preferred).
  • Minimum8+ of progressively responsible packaging engineering experience preferably within the medical device, pharmaceutical, or regulated healthcare industry.
  • Demonstrated experience leading complex packaging development and validation programs from concept through commercialization.
  • Proven track record influencing technical decisions across cross-functional teams.
  • Certified Packaging Professional (CPP) or equivalent professional certification (preferred).
  • Experience supporting Class II and Class III medical devices (preferred).
  • Experience working in global manufacturing environments (preferred).
  • Experience leading or mentoring engineering teams (preferred).

Technical Expertise
  • Expert knowledge of ISO 11607 Parts 1 & 2, ISO 13485, ASTM packaging standards, Medical device packaging validation methodologies, Sterile barrier systems, Cleanroom packaging processes and Labeling regulations and UDI requirements
  • Strong understanding of Design Controls, Risk Management (ISO 14971), CAPA systems, Change Control, Complaint Investigations and Validation requirements

Analytical Skills
  • Advanced statistical analysis capability using Minitab or equivalent tools.
  • Process capability analysis and design of experiments (DOE).
  • Root cause investigation and structured problem-solving methodologies.
  • Ability to interpret complex technical data and make risk-based decisions.

Leadership Skills
  • Ability to influence without direct authority.
  • Strong project leadership and stakeholder management skills.
  • Effective mentoring and coaching of engineering personnel.
  • Strong presentation and communication skills with senior management and external stakeholders.

Preferred Software Proficiency in Minitab, SAP and/or PLM systems, Labeling systems, SolidWorks, AutoCAD, TOPS, CAPE, Microsoft Office Suite and Statistical and data analysis software
Salary range: $120k -$145k plus bonus targeted at 10% (depending on overall company performance)
#LI-LG1
About us
With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.
Benefits at Getinge:
At Getinge, we offer a comprehensive benefits package, which includes:
  • Health, Dental, and Vision insurance benefits
  • 401k plan with company match
  • Paid Time Off
  • Wellness initiative & Health Assistance Resources
  • Life Insurance
  • Short and Long Term Disability Benefits
  • Health and Dependent Care Flexible Spending Accounts
  • Commuter Benefits
  • Parental and Caregiver Leave
  • Tuition Reimbursement

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.

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About Getinge

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Dr Wayne, NJ, US

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