Senior Plastics Injection Molding & Tooling Engineer

The Senior Plastics Injection Molding Tooling Engineerprovides seniorlevel technical expertise in injection molding processes and tooling engineering to support the manufacture of highprecision medical devices. This role is responsible for sustaining engineering support and driving continuous improvement initiatives to achieve safety, quality, delivery, and cost objectives within a regulated medical device manufacturing environment.

The position partners closely with New Product Introduction (NPI) and sustaining engineering teams, serving as a technical advisor on plastic part design and supporting mold builder selection, mold design, build oversight, performance testing, and process optimization for new tooling.

The role also supports validation activities for new molds as well as verification and change management for legacy tooling. In addition, the Senior Plastics Injection Molding Tooling Engineer supports injection molding process and tooling personnel by developing, optimizing, documenting, and implementing robust molding and tooling processes. The role is accountable for mold preventive maintenance and repair programs, tooling reliability, and the establishment and management of mold spare parts programs.

Key Duties and Responsibilities:

Molding & Tooling Engineering

Design, develop, qualify, and optimize molding processes used to manufacture complex, high-precision medical device components, ensuring compliance with regulatory and quality system requirements.

Lead tooling design, modification, validation, and maintenance activities, including molds, fixtures, and gauges, to support production and product quality.

Specify, evaluate, and implement new moldingequipment, tooling, and technologies to improve capability, efficiency, and cost performance.

Process Development & Sustaining Engineering

Investigate and resolve molding and tooling-related manufacturing issues to minimize downtime and ensure site safety, quality, delivery, and cost objectives are achieved.

Develop, introduce, and document process improvements, including engineering change orders (ECOs), process parameters, work instructions, and validation documentation.

Provide technical support to production teams and High-Performance Work Teams on the manufacturing floor.

New Product Introduction (NPI) & Validation

Support new product introductions by developing molding and tooling strategies, process flows, and validation plans.

Execute and support IQ/OQ/PQ activities, tooling qualifications, and vendor qualifications in accordance with internal procedures and regulatory requirements.

Partner with R&D, Quality, and Operations to transfer products from development to full-scale manufacturing.

Continuous Improvement & Leadership

Lead and participate in continuous improvement, cost reduction, and yield improvement initiatives using structured problem-solving and statistical tools.

Mentor and provide technical guidance to less experienced engineers and technicians in molding and tooling disciplines.

Lead engineering projects, ensuring assigned deliverables, timelines, and objectives are met.

Documentation & Collaboration

Maintain accurate engineering documentation, files, logs, reports, and records as required.

Interface with internal and externalsuppliers, tooling vendors, and cross-functional partners to resolve technical issues and support business objectives.

Perform other related duties as assigned based on business needs.

Expected Travel 0-20%

Minimum Qualifications

• Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Plastics Engineering, or a related engineering discipline.

• Minimum 5 years of progressive experience in plastics injection molding and tooling engineering ideally with development, validation, and process optimization, preferably within the medical device or regulated manufacturing environment, including project management experience.

Preferred Experience:

• Strong knowledge of plastic molding processes (e.g., injection molding) and tooling design principles.

• Proficiency interpreting engineering drawings and using CAD tools.

• Working knowledge of process validation, statistical analysis, and continuous improvement methodologies.

• Advanced engineering degree.

• Experience supporting regulated manufacturing under FDA/QSR and ISO requirements.

• Demonstrated ability to lead cross-functional technical projects.

This position is not eligible for employer-visa sponsorship

Disclosure as required by applicablelaw, the annual salary range for this position is $87,600 - $135,800. The actual compensation may vary based on geographic location, work experience, education and skill level. The salary range is CONMED's good faith belief at the time of this posting.

This job posting is anticipated to close on June 6, 2026. We may, however, extend this time period, in which case the posting will remain available on careers.conmed.com. Please submit your application as soon as possible as we will be reviewing applications on a rolling basis as we receive them.

Benefits:

CONMED offers a wide array of benefits to fit your unique needs. Visit our Benefits Page for more information.

• Competitive compensation
• Excellent healthcare including medical, dental, vision and prescription coverage
• Short & long term disability plus life insurance -- cost paid fully by CONMED
• Retirement Savings Plan (401K) -- CONMED matches your contributions dollar for dollar, with the potential for up to 7% per pay period
• Employee Stock Purchase Plan -- allows stock purchases at discounted price
• Tuition assistance for undergraduate and graduate level courses

Know someone at CONMED? Have them submit you as a referral before applying for this position to be eligible for our Employee Referral Program incentives!

CONMED is an equal opportunity employer and does not discriminate on the basis of any legally protected status or characteristic. Protected veterans and individuals with disabilities are encouraged to apply. The Know Your Rights: Workplace Discrimination is Illegal Poster reaffirms this commitment.

Colorado Residents: In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

If you feel you need a reasonable accommodation pursuant to the ADA, you are encouraged to contact us at 800-929-7176 option #5.