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Sr. Engineer I - Packaging

Arthrex · Naples, FL1mo agoverified 8 h ago

BS-level Product Development roles on Crosslinked list a median of $118k (200 that show pay). This posting does not list pay.

Develop and validate sterile/non-sterile packaging designs and materials for orthopedic medical devices

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Worth knowing

Why it is interesting. Lead packaging design and validation for sterile orthopedic devices, from material selection through 510(k) submission support.

Might not be for you. Packaging-engineering focused with heavy documentation, CAPA, and regulatory work — not polymer R&D or formulation.

Deep specialist Senior hires only

Adjacent materials roleSelect appropriate packaging materials based on product and sterilization requirements; researching new packaging materials; sterile barrier protection

Seniority
Senior
Work
On-site
Type
Full-time
Degree
BS
Experience
5+ yrs
Industry
Medical devices
Role
Product Development
Benefits
free onsite lunchfree onsite medical clinicstuition reimbursement

Role details

Requisition ID

65496

Title

Sr. Engineer I - Packaging

*Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a Sr. Engineer I - Packaging. This individual will provide packaging engineering support for design engineering projects, as well as support and assist packaging engineering development goals in support of overall business goals. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.*

Essential Duties And Responsibilities

  • Coordinate Packaging Development activities for new MPI’s and product improvement projects. This may include but is not limited to the following:
  • Create and maintain packaging engineering specifications utilizing CAD, 3D modeling software, or other software tools.
  • Create and maintain packaging designs for sterile and non-sterile products.
  • Select appropriate packaging materials based on product and sterilization requirements.
  • Create and maintain Packaging Instruction documents for the final manufacturing packaging assembly of finished devices.
  • Communicate (not execute) packaging process validation activities with manufacturing or designated design team member for Arthrex products.
  • Coordinate and execute packaging design validation activities post packaging process approval.
  • Oversee any required package testing to assure viability of packaging/product construct for sterile and non-sterile barrier protection.
  • Generating protocols, test reports, and engineering adoptions and maintenance of test documentation per approved documentation system per quality standards.
  • Ensure essential packaging development activities are completed prior to packaging design transfer activities.
  • Coordinate Instrument Case development activities for new MPI’s and product improvement projects. This may include but is not limited to the following:
  • Coordinate and Create Instrument Case Layouts with Design Team and Contract Suppliers.
  • Create and maintain Instrument Case Specifications.
  • Oversee Design Verification and Validation activities for Instrument Cases.
  • Lead Instrument Case project when Instrument Case is a standalone MPI.
  • Provide support for packaging engineering related CAPA’s.
  • Provide supporting packaging documentation to Regulatory and Quality for 510(k) and ERC submissions and audits.
  • Create Bill of Materials and generate Engineering Change Orders (ECO) in support of new products and various revisions or maintenance.
  • Communicate effectively with Design Team members and Contract Suppliers using project management tools, written, and verbal communication.
  • Support product design changes to develop and improve existing products that affect existing packaging.
  • Oversee any required package testing to assure viability of packaging/product construct and sterile barrier protection. This includes
  • Provide supporting packaging documentation to Regulatory and Quality for 510(k) and ERC submissions and audits.
  • Create Bill of Materials and generate Engineering Change Orders (ECO) in support of new products and various revisions or maintenance.
  • Communicate effectively with Design Teams and Contract Suppliers using project management tools, written, and verbal communication.

Skills

  • Advanced capabilities in designing complex packaging designs and packaging instructions using a CAD program (AutoCAD or Solidworks) required.
  • Proficient at leading DHF projects for Packaging only and Instrument Case projects.
  • Advanced knowledge of packaging validation process as required by quality and regulatory standards.
  • Advanced capabilities of researching new packaging materials and suppliers for manufacturing process improvements and/or cost reductions.
  • Advanced capabilities in leading Global Packaging Projects for design and/or packaging process improvements.
  • Advanced ability of writing and approving technical documentation internally.
  • Advanced capability of reviewing and approving technical documentation from external packaging subcontractors.
  • Able to coach, mentor, and supervise technicians and/or junior packaging engineers.
  • Proficient at creating packaging procedures and providing training on procedures.
  • Advanced knowledge of design and manufacturing processes and ability to incorporate improvements into designs
  • Proficient at specifying and communicating design, process, or other packaging related improvements with manufacturing and contract packagers.
  • Proficient at supporting and participating in internal and external audits in support of regulatory compliance.

Knowledge

  • Complete understanding and application of principles, concepts, practices, and standards. Full knowledge of industry practices.

Education/Experience

  • Bachelor’s degree in Engineering required; preferably in Packaging Engineering.
  • Minimum of 5 years’ experience in Packaging Design and Development or Manufacturing required.
  • Medical device packaging or manufacturing environment experience preferred.

Arthrex Benefits

  • Medical, Dental and Vision Insurance
  • Company-Provided Life Insurance
  • Voluntary Life Insurance
  • Flexible Spending Account (FSA)
  • Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness)
  • Matching 401(k) Retirement Plan
  • Annual Bonus
  • Wellness Incentive Program
  • Free Onsite Medical Clinics
  • Free Onsite Lunch
  • Tuition Reimbursement Program
  • Trip of a Lifetime
  • Paid Parental Leave
  • Paid Time Off
  • Volunteer PTO
  • Employee Assistance Provider (EAP)
  • Deferred Compensation Plan (DCP)

All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law.

Related roles

Common questions

Does Arthrex sponsor H-1B visas?

Arthrex has filed H-1B petitions with the US Department of Labor in past years, but this specific posting does not explicitly mention sponsorship for the Sr. Engineer I - Packaging role. Confirm with the employer before applying if visa support is required.

Where is the Sr. Engineer I - Packaging role at Arthrex based?

This role is based in Naples, FL.

What degree is required for the Sr. Engineer I - Packaging role at Arthrex?

This role requires a BS.

How many years of experience does this Sr. Engineer I - Packaging role require?

The posting calls for at least 5 years of relevant experience.