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Sterile Packaging Jobs (NOW HIRING)

Red Star

Sterile Packaging Manager

IN · On-site

The Sterile Packaging Manager leads and oversees sterile packaging activities. This role partners cross-functionally with Regulatory, Product Development, Operations, Supply Chain, and Quality to ...

Red Star

Sterile Packaging Manager

Larwill, IN · On-site

The Sterile Packaging Manager leads and oversees sterile packaging activities. This role partners cross-functionally with Regulatory, Product Development, Operations, Supply Chain, and Quality to ...

Red Star

Senior Sterile Packaging Engineer

IN · On-site

The Senior Sterile Packaging Engineer serves as the technical lead and subject matter expert for sterile packaging activities. This role partners cross-functionally with Regulatory, Product ...

Amaris Consulting

Packaging Engineer

Warsaw, IN · On-site

Academic or practical experience with medical device packaging, sterile packaging, packaging design, testing, or validation is welcome. * Duration: 12 months * Employment type: C2C / freelance

Marmon

Clean & Packaging Technician 1

Addison, TX

$16.50 - $20/hr

Job Scope The Clean & Packaging Technician is responsible for the cleaning, label printing, and packaging of both non-sterile and sterile medical devices. Shift: Monday through Friday, 6:00am - 2 ...

Marmon

Clean & Packaging Technician 1

Addison, TX · On-site

$16.50 - $20/hr

Job Scope The Clean & Packaging Technician is responsible for the cleaning, label printing, and packaging of both non-sterile and sterile medical devices. Shift: Monday through Friday, 6:00am - 2 ...

Medtronic

Packaging Engineer II

Lafayette, CO · On-site

Support the design, development, and implementation of sterile and non-sterile packaging systems for new and existing products. * Prepare and execute packaging validation protocols, testing ...

Medtronic

Packaging Engineer II

Lafayette, CO · On-site

Support the design, development, and implementation of sterile and non-sterile packaging systems for new and existing products. * Prepare and execute packaging validation protocols, testing ...

Medtronic

Packaging Engineer II

Lafayette, CO · On-site

Support the design, development, and implementation of sterile and non-sterile packaging systems for new and existing products. * Prepare and execute packaging validation protocols, testing ...

Medtronic

Sr Packaging Engineer

Dexter, MI · On-site

Responsibilities include sterile barrier design, packaging validation, sustaining engineering activities, compliance initiatives, and manufacturing support. This position is based in Dexter, Michigan.

MicroVention

Staff Engineer, Packaging

Aliso Viejo, CA · On-site

$116K - $153K/yr

Support sterile and non-sterile packaging systems for new products, product changes, line extensions, and sustaining engineering activities. * Develop, review, and maintain packaging documentation ...

Medtronic

Sr Packaging Engineer

Dexter, MI · On-site

Responsibilities include sterile barrier design, packaging validation, sustaining engineering activities, compliance initiatives, and manufacturing support. This position is based in Dexter, Michigan.

Medtronic

Sr Packaging Engineer

Dexter, MI · On-site

Responsibilities include sterile barrier design, packaging validation, sustaining engineering activities, compliance initiatives, and manufacturing support. This position is based in Dexter, Michigan.

Stryker

Senior Medical Packaging Engineer

Tempe, AZ · On-site

$77K - $129K/yr

Design and develop sterile packaging components and systems, translating user needs into engineering specifications * Create and execute packaging validation and verification protocols in alignment ...

Stryker

Senior Medical Packaging Engineer

Tempe, AZ · On-site

$77K - $129K/yr

Design and develop sterile packaging components and systems, translating user needs into engineering specifications * Create and execute packaging validation and verification protocols in alignment ...

Imperative Care

Sr Packaging Engineer

Campbell, CA · On-site

$132K - $158K/yr

Design and develop sterile and non-sterile packaging systems for medical devices and capital equipment products. * Participate in design reviews, risk assessments, human factors evaluations, and ...

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Sterile Packaging information

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How much do sterile packaging jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for sterile packaging in the United States is $27.49, according to ZipRecruiter salary data. Most workers in this role earn between $19.95 and $33.17 per hour, depending on experience, location, and employer.

What is sterile packaging?

A Sterile Packaging job involves assembling, inspecting, and sealing medical devices or pharmaceutical products in a contamination-free environment to ensure they remain sterile until use. Workers follow strict regulatory guidelines, such as FDA or ISO standards, to maintain product integrity. This role typically requires attention to detail, adherence to cleanliness protocols, and sometimes working in a cleanroom setting.

What does someone in sterile packaging do?

In a Sterile Packaging role, your main responsibilities include preparing, inspecting, and packaging medical instruments or products in a controlled cleanroom environment to ensure sterility. You will operate specialized equipment such as autoclaves and heat sealers, document batch records, and follow strict protocols to comply with industry regulations. Additional duties may involve performing routine quality checks, replenishing supplies, and coordinating with quality assurance and production teams to maintain workflow. This role is detail-oriented and essential for protecting patient safety and upholding organizational standards.

What are the key skills and qualifications needed to thrive in sterile packaging?

To excel in Sterile Packaging, strong attention to detail, manual dexterity, and knowledge of sterile techniques are crucial, often complemented by a high school diploma or relevant technical training. Familiarity with autoclaves, heat sealers, and industry-standard sterilization protocols such as ISO 11607 is typically required, with some employers preferring certification in sterile processing. Teamwork, reliability, and effective communication stand out as valuable soft skills in this environment. These abilities are vital to ensure the integrity of sterile products, regulatory compliance, and patient safety in healthcare or manufacturing settings.

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Sterile Packaging jobs near you
Infographic showing various Sterile Packaging job openings in the United States as of September 2026, with employment types broken down into 84% Full Time, 10% Part Time, 1% Temporary, 2% Contract, and 3% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $57,186 per year, or $27.5 per hour.

Sterile Packaging Manager

IN • On-site

Red Star
Restaurants • 51 - 200 employees
Learn more about Red Starexternal

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 22 days ago

Job description

ABOUT US: Red Star is a vertically integrated U.S.-based contract manufacturer specializing in injection molding, precision machining, cleanroom assembly, and sterile packaging for the medical device industry. From concept through high-volume production, our teams work together to solve complex manufacturing challenges and help bring innovative medical devices to market.
SUMMARY: The Sterile Packaging Manager leads and oversees sterile packaging activities. This role partners cross-functionally with Regulatory, Product Development, Operations, Supply Chain, and Quality to develop and execute sterile packaging strategies from concept through commercialization and post-market support. Serving as an organizational subject matter expert, this position ensures sterile packaged products meet requirements for sterility assurance, packaging integrity, shelf life, transportation, distribution, and regulatory compliance.
The Sterile Packaging Manager provides leadership for packaging design and development, validation strategy, process controls, and technical documentation, including Design History File (DHF) requirements. The role establishes procedures and standards related to sterile packaging while leading continuous improvement initiatives and developing team members and cross-functional project teams.
ESSENTIAL DUTIES AND RESPONSIBILITIES: (includes the following but other duties may be assigned)
  • Lead the strategy, development, implementation, and lifecycle management of sterile packaging designs across product lines in partnership with product development teams to ensure packaging, labeling, and sterilization requirements are achieved.
  • Lead sterile packaging activities and provide coordination for sterilization requirements for new product introductions, design changes, and sustaining engineering initiatives.
  • Oversee the design, evaluation, and approval of packaging components and sterile packaging systems for medical device products.
  • Review, approve, and maintain packaging, labeling, and related technical documentation to ensure compliance with applicable requirements.
  • Lead risk assessment activities related to product, packaging, sterilization, and process changes to maintain sterility assurance and package integrity across all applicable entities.
  • Establish validation strategies and oversee execution of sterile packaging-related validation and verification activities, including sealing validations, OQ/PQ studies, design of experiments, transit testing, aging studies, and ongoing process monitoring.
  • Ensure effective monitoring, control, and continuous improvement of sterile packaging processes across internal and external manufacturing locations.
  • Develop and maintain procedures, business processes, work instructions, and training programs related to sterile packaging and sterilization activities.
  • Provide leadership and technical oversight for creation and approval of protocols, reports, technical justifications, and validation documentation.
  • Ensure packaging validation programs remain current, effective, and compliant at all applicable facilities.
  • Lead design transfer activities and ensure critical process parameters are defined, documented, transferred, and controlled based on process capability and risk.
  • Partner with Operations to optimize sterile packaging equipment, manufacturing processes, and production readiness while providing technical consultation to contract manufacturing partners and customers as needed.
  • Manage sterile packaging project timelines, priorities, and resource allocation to support business objectives and product launch commitments.
  • Lead investigations and corrective actions associated with post-market surveillance signals, nonconformances, and quality events related to sterile packaging.
  • Represent sterile packaging functions during customer, internal, regulatory, and certification audits.
  • Supervise, coach, and develop assigned team members and provide leadership to cross-functional project teams.

QUALIFICATION REQUIREMENTS:
  • Bachelor's degree in Packaging Engineering, Packaging Science, Engineering, or related technical discipline.
  • Minimum 5-7 years of progressive experience in sterile packaging within medical device, pharmaceutical, or related regulated industry; medical device experience strongly preferred.
  • Previous experience leading projects, initiatives, teams, or direct reports preferred.

OTHER SKILLS and ABILITIES:
  • Strong leadership, project management, and cross-functional collaboration skills.
  • Knowledge of applicable standards including ISO 11607, ISO 11137, relevant ASTM standards, and quality system requirements.
  • Experience with manufacturing processes, process validation, statistical analysis, and risk management methodologies.
  • Ability to influence decision-making and drive execution across multiple stakeholders and facilities.

BENEFITS:
  • Health, dental, and vision insurance
  • Paid time off and paid holidays
  • 401(k) with company match
  • Bonus opportunities

PHYSICAL DEMANDS AND WORK ENVIRONMENT:
While performing the duties of this job, the employee is regularly required to sit, talk, and hear. The employee is frequently required to stand, walk, and use hands to handle or feel objects, tools, or controls. The employee may occasionally be required to reach with hands and arms and lift and/or move up to 20 pounds.
The employee will typically work in a manufacturing environment and may be exposed to high noise levels from machinery, moving machine parts, and other physical hazards. The physical demands and work environment characteristics described here are representative of those an employee may encounter while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

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