Staff Engineer, Electromechanical Design

Bayer•Pittsburgh, PA

About The Position

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where 'Health for all Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice. Staff Engineer, Electromechanical Design Position Overview: As a Staff Engineer, Electromechanical Design, you are responsible for applying your technical expertise to shape and execute test strategies, lead system test development, and implement advanced manufacturing solutions. You will take ownership of medium- to high-complexity projects, aligning test systems with strategic business goals. Your work will drive innovation, support new technology adoption, and promote Design for Excellence (DfX) principles throughout the product development lifecycle. This position will be located in Pittsburgh, PA and will require some travel (up to 20%). This position is part of the CMC&T Medical Devices & Combination Products (MDCP) cluster within our Device Automation Capabilities team. The Device Automation Team is responsible for developing and managing automated assembly, testing, and packaging solutions for medical devices, ensuring regulatory compliance, operational efficiency, and robust lifecycle support. The team plays a critical role in new product introduction, life cycle engineering changes, and delivers technical leadership for complex automation projects in collaboration with trusted partners.

Requirements

Minimum of a Bachelor's Degree or an equivalent combination of education and experience (High School Diploma + 5 years of relevant industry experience will be accepted in lieu of a Bachelor's Degree);
Industry experience in the medical device sector (or other heavily regulated industry), with hands-on involvement in systems, test processes, and methods across multiple specialties including process manufacturing, electromechanical engineering, and Design for Excellence (DfX) (or disciplines related to DfX);
Experience in defining requirements specification and design details for test systems of medical devices in a manufacturing environment;
Knowledge of best practices in software development lifecycle with proven ability in multiple languages (e.g., C, Java, or C#);
Familiarity with MCAD and ECAD tools;
Proficient in statistical analysis and the use of statistical tools to interpret data, identify trends, and implement solutions that enhance accuracy and efficiency in systems testing;
Proven track record of leading and mentoring teams, either in peer-to-peer settings or as a direct manager;
Some experience managing end-to-end (E2E) projects of medium to high complexity, particularly in new product development and design control environments;
Strong technical foundation with the ability to apply pragmatic and creative problem-solving methods in dynamic and fast-paced environments.

Nice To Haves

At least 4 years of relevant industry experience in the medical device sector (or other heavily regulated industry), with hands-on involvement in systems, test processes, and methods across multiple specialties including process manufacturing, electromechanical engineering, and Design for Excellence (DfX) (or disciplines related to DfX);
Experience developing dashboards in an informatics tool such as Power BI or Tableau.

Responsibilities

Innovate: Develop and implement system test solutions for complex electromechanical assemblies and combination products; stay ahead of emerging technologies and methodologies to enhance our manufacturing capabilities;
Lead: Review and analyze system specifications; spearhead the development of next-generation test equipment fixtures and processes, identifying opportunities and risks to ensure the successful launch of medical devices;
Collaborate: Work closely with cross-functional teams, external partners, and manufacturing sites to deliver projects on time and within budget, minimizing disruptions;
Educate: Mentor junior engineers and promote DfX initiatives to foster a culture of excellence in product development;
Execute: Create and maintain comprehensive technical documentation, ensuring compliance with safety, quality, and regulatory standards; execute test cases (manual or automated), analyze results, and document test reports.