• Impact Business Group
  • $92,230.00 -143,150.00/year*
  • Mesa, AZ
  • Engineering
  • Full-Time
  • 1017 S Gilbert Rd

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Excellent Opportunity with Global Fortune 300 Medical Device Organization!

Sr. Staff Laboratory Cleaning Process Engineer

Located in Tempe AZ

Great Career Advancement Opportunities

Relocation Assistance Available

Summary of Position

Responsible for creating a work practice and environment that pushes the boundaries of conventional manufacturing & metrology, specifically in product cleaning processes and technologies.
Executes the innovation and development of new products with an emphasis on manufacturing processes, technologies and procedures.
Role success will be gauged by this individual s contribution in coaching the engineering team to effectively meet and/or exceed new product metrics including product cost, process performance and time to market.
Essential Duties & Responsibilities:
Serve as subject matter expert in cleaning methodologies and process development.
Provide expertise in cleaning agent selection, cleaning process technologies and cleaning process optimization.
Determines the technical objectives of engineering assignments and makes decisions regarding the direction and the results of the assignment.
Will monitor and control progress of work ensuring sound application of engineering principles and the appropriate use of policies and procedures.
Lead capital acquisition activity of cleaning process equipment from specifying equipment, contract negotiation, installation and validation.
Will analyze cleaning equipment to establish operating data, conduct experimental test and result analysis. May lead or act as independent reviewer in process review meetings.
Will coach and mentor others on functionally related topics.
Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with new product development procedures.
Ensure quality of process and product as defined in the appropriate operation and material specifications.
Participate in PFMEA, Control Plan and SOP generation associated with product transfers and launches.
Ensure adherence to GMP and safety procedures.
Review and approval of validation documentation.
Drive and execute effective communication with all stakeholders to enable project success.
All other duties as assigned.
Bachelor s Degree along with 5-7+ years experience


* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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