Minimum Requirements

• Senior level individual contributor on a project or work team, 5+ Years of experience required.
• Bachelor Degree in Engineering
• Strong experience within Medical Devices and/or Pharmaceutical industries. Exposure to engineering and manufacturing environment.
• Performs Validation & CSV Activities, Characterization, Process Qualifications, and Equipment Qualification (new equipment and equipment changes).
• Develops expertise knowledge of all factors that make a process to support the response to highly technical questions and situations, to solve quality issues, to improve process, or to confirm reliability of products.
• Collaborates with technical experts, design team, and other facilities for the process development of new devices.
• Supports process owners. 
• Works on complex problems where analysis of situations or data requires an evaluation of many tangible and intangible factors.
• Make complex technical recommendations on product quality and reliability to sustain business activities.
• Transfers new product and test technologies from other site facilities to the business unit assigned or from Vendor to site
• Monitors test system performance using Statistical Tools.
• Delivers work of significant scope and makes changes in systems and processes to solve problems .
• Quality mindset to improve and deliver results.
• Computer literacy in MS Word, Excel, PowerPoint, preferably experience with Minitab
• Ability to speak, write and understand English to comply with written procedures, instructions, SOPs and other technical documents.

**Weil Group is proud to be an Equal Employment Opportunity Employer**