Sr. Engineer Manufacturing - Medical Devices

About Us

Founded in 1908, Merz is a successful, family‑owned specialty healthcare company with a rich history. As a leading global aesthetics business, our award‑winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine. Our purpose is to fuel confidence by helping people look better, feel better, and live better. We believe you do not have to choose between living life and making a living.

Live your best life with Merz Aesthetics.

An experienced engineer, with a device engineering foundation in a regulated environment heavily focused on manufacturing processes (validation, qualification, process improvements, design transfer, efficiency, supplier management). Ensures process qualification, product reliability, manufacturability, and regulatory compliance are maintained, through cross‑functional collaboration, rigorous testing, and continuous process improvement. Able to work with minimal guidance on larger process/product improvements while providing indirect mentorship.

• Manufacturing and Sustaining Focus Support production critical manufacturing and supply continuity issues. Lead and manage complex and critical activities related to maintaining and improving electro‑mechanical medical device manufacturing, process optimization, and design via internal and Contract Manufacturing Organizations. Lead, with minimal oversight, the implementation of manufacturing equipment, process expansions, new initiatives, and process automation. Includes project budgeting, design & interfacing with vendors of equipment and tooling, and maintaining appropriate documentation for new equipment and processes including qualification, verification, and validation.
  
  Lead troubleshooting activities, investigate the root cause to a successful conclusion, and help to resolve manufacturing process related issues, product complaints and CAPA.
• Process Improvements Lead and identify improvements in manufacturing equipment/process and product design to improve productivity and quality of current and future products while expecting cost reductions.
• Collaboration Work closely with cross‑functional teams, including mechanical and electrical engineers, contract manufacturing organizations, quality, suppliers, and regulatory, to ensure device safety, manufacturability, compliance, compatibility, functionality, and serviceability.
• Regulatory Compliance Ensure that device complies with relevant regulations and standards (e.g., FDA, CE Mark, IEC 60601 series, ISO 13485, GMP).
• Documentation Develop and maintain detailed drawings. Documentation of design processes and test results. Execute the Engineering Change Order (ECO) process per Design Controls – Design Change regulations and internal policies. Support regulatory submissions.
• Leadership Indirectly mentor junior engineers. Proactively identify process improvements through proposal of resources, budget, risk, and return on investment.
• Other Duties Assigned Perform other duties as needed including review of test. Plans and reports, maintaining project deliverables, and other general engineering related tasks.

• Bachelor's Degree in Biomedical, Industrial, Manufacturing, Electrical, or Mechanical Engineering.
• 7+ years Experience in a regulated industry.
• 3-5 years Experience in manufacturing/support, systems, or sustaining.

• Master's Degree in Biomedical, Industrial, Manufacturing, Electrical, or Mechanical Engineering.
• 8-10 years experience.
• Majority experience in the healthcare industry specifically with electro‑mechanical devices directly managing manufacturing operations.
• Experience with ultrasound technologies.

• Demonstrated ability to lead projects with large scope and high technical complexity.
• Strong technical and problem‑solving skills.
• Ability to communicate and write effectively.
• Emotional self‑management in difficult situations.
• Understanding and application of process validation and statistical analysis.
• Understanding and application of ISO 13485 quality management system requirements.
• Understanding…