- 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.
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Sr Manufacturing Engineer - Juncos, Puerto Rico - Weil Group, Inc
Descripción
Minimum Requirements
**Weil Group is proud to be an Equal Employment Opportunity Employer**
