Senior Quality Engineer

Merz Pharmaceuticals USA-posted 2 months ago
Full-time • Mid Level
Franksville, WI
501-1,000 employees
Professional, Scientific, and Technical Services
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This position is responsible for providing Quality Engineering and Technical Support for Operations, Sustaining Engineering, R&D, and New Product Introductions. This position would include supporting a wide array of activities related to Change Control, NCR/CAPA, Quality Operations, Design Control, New Product Development, Risk Management and Post Market Surveillance. This position would evaluate the operation of Manufacturing and Quality activities in relation to compliance to Quality Standards and Regulations and recommend where corrections or improvements are needed. Provide direct support to Quality personnel regarding operation of the department and Quality System. Provide support to other departmental activities as directed.

  • Review change requests and identify impact on product design and documentation.
  • Support Change Control Activities (Operations, Engineering, Design, etc.).
  • Support updates to manufacturing procedures, process, product/specifications, risk management files, etc. through the Change Control process.
  • Support 3rd party supplier management activities such as review 3rd party design control activities.
  • Review documentation for technical accuracy and compliance to procedures.
  • Review Technical Writing and Documentation.
  • Support operations, sustaining engineer, R&D and NPI departments in the development, verification and validation of product changes and introduction of new products.
  • Provide quality engineering support for supplier changes and resolution of issues at suppliers.
  • Identify new quality improvement initiatives/projects in accordance with cGMP expectations to improve compliance, quality levels (reducing defects), and improve operational efficiencies.
  • Work with manufacturing and other functional groups on manufacturing regulatory compliance issues.
  • Support training program by delivering assigned training tasks.
  • Support/lead corrective/preventive actions and product non-conformances including capturing data and investigations associated with product deviations, product non-conformances, CAPAs, scrap and rework, and analyzing the data for the reasons of Quality Improvement and reporting.
  • Support Risk Management activities including review and coordination of quality activities related to risk.
  • Support with federal, state, and local regulatory officials during regulatory inspections.
  • Support in internal and vendor quality system audits as applicable.
  • Assist with adherence to all Federal, State and Local Regulations controlling the manufacture of Electromechanical Devices (EMD) and non-EMD medical devices.
  • Provide support to Quality Management personnel and perform other duties as assigned.
  • Bachelor of Science (B.S.) Physical Science or Engineering, or equivalent experience.
  • 3-5 years Quality Engineering Role.
  • 6-7 years Medical Device or Pharmaceutical Industry or similar experience.
  • Working with electromechanical devices.
  • ASQ Certification as a Quality Engineer or equivalent.
  • Comprehensive Medical, Dental, and Vision plans
  • 20 days of Paid Time Off
  • 15 paid holidays
  • Paid Sick Leave
  • Paid Parental Leave
  • 401(k)
  • Employee bonuses
  • And more!
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