Senior Engineer​/Scientist

Salary Range: $96,731.00 To $ Annually

As a Pro Med employee, you will contribute to the manufacture of products that have a significant impact on people’s lives. Through honesty, integrity, and collaboration, we strive to be the very best as we hire the very best.

Pro Med was founded in 1989 addressing an industry need for cleanroom manufacturing of silicone components, specifically those having a medical application. We treat every component and finished device as though it will be used by a beloved family member or friend. We are dedicated to our customers and to our employees while helping to improve the health and well-being of people around the world.

Working as one to help many.

WHY THIS ROLE MATTERS

The mission of this role is to translate complex pharmaceutical and medical device concepts into robust, scalable manufacturing processes that meet stringent regulatory standards and customer specifications. This position drives organizational value by ensuring seamless transition of development projects from feasibility through validation, directly impacting commercial readiness and time-to-market for critical healthcare products. Through rigorous application of statistical process optimization and Design of Experiments methodologies, the role establishes manufacturing excellence that reduces production risk and enhances operational efficiency.

Additionally, this position strengthens organizational capability by providing technical leadership across cross-functional teams and mentoring engineering staff, building the deep process knowledge essential for sustained competitive advantage in the medical device manufacturing sector.

WHAT YOU’LL ACHIEVE

While the ways that you fulfill these responsibilities will likely evolve, your core responsibilities are:

Drive process development and optimization for combination medical devices and pharmaceutical products to enable efficient manufacturing, resulting in validated processes that meet clinical and commercial production requirements

On average this should be about 30% of your time. Among other things this means we expect you to:

• Execute equipment and process qualification and validation protocols
• Collaborate with Operations to scale up processes from development to commercial manufacturing
• Lead design, execution, and analysis of Design of Experiments (DoEs) to identify optimal process parameters
• Develop and optimize pilot processes that meet customer specifications and regulatory requirements
• Lead technical problem-solving efforts to resolve process challenges and improve efficiency

Establish technical project leadership across feasibility and development initiatives to deliver customer solutions, resulting in successful project execution and client satisfaction

On average this should be about 25% of your time. Among other things this means we expect you to:

• Partner with Business Development to create technical proposals for customer projects
• Manage multiple concurrent feasibility projects with competing priorities
• Identify new technical resources and approaches to expand capabilities and grow expertise
• Take independent ownership of large development and clinical projects from concept through completion
• Communicate project status and technical findings effectively to internal teams and clients

Create comprehensive technical documentation and manufacturing specifications to ensure process consistency and regulatory compliance, resulting in complete batch records and quality systems that support production operations

On average this should be about 20% of your time. Among other things this means we expect you to:

• Collaborate with Project Management, Operations, and Quality to complete key documentation tasks
• Create efficient batch records, materials…