Imagine working for one of the leading contract manufacturers in the world. Trelleborg Healthcare and Medical is located 30 miles from California’s pristine Central Coast. As a premier manufacturer for life-saving medical components, Trelleborg Healthcare and Medical is a forward thinking company. We have been active in our lean manufacturing journey for many years and are advancing towards making our business a showcase of excellence in the medical industry.
Seize this rare opportunity to be part of a healthcare and medical business unit that has been in business for over 100 years, all while enjoying the benefits of living in one of California’s most desired locations!
As a valued Trelleborg team member, you will enjoy:
- Greater opportunity for impact;
- Competitive compensation;
- Outstanding benefits package: Health, Dental, Vision, STD, LTD, Life, 401k;
- Generous paid time off;
- Bonus potential
Trelleborg Healthcare and Medical is seeking a Manufacturing Engineer. In this role, you will follow good manufacturing practices (GMP) and principles to provide engineering support and develop robust manufacturing processes. Has a primary role in the engineering of new, modified and/or existing manufacturing operations in a clean-room environment.
Essential Functions:
- Analyzes new product specifications and translates these into manufacturing processes to establish production rates, achieve expected quality levels and establish the reliability of the finished product.
- Responsible for the completion of the design and development of optimal, cost-effective, and reliable manufacturing processes.
- Use demonstrated strengths in multiple aspects of medical component and device design and manufacturing capabilities to plan and accomplish goals.
- Develops process parameters, procedures, and related documentation
- Conducts data analysis and collaboration with Operations and Quality Engineering.
- Identifies Operational Qualification (OQ) process parameters and Performance Qualification (PQ) settings.
- Develops and documents standard operating procedures (SOP) and product-specific operating procedures (PSOP).
- Trains manufacturing personnel on SOPs and PSOPs.
- Performs DOEs, and participates in the development of control plans, Process Maps, and PFMEA documentation.
- Organizes internal cross-functional teams and corresponding outside vendors needed to meet project needs. Procures equipment as needed.
- Uses standard problem-solving tools, e.g., 8D, 5 Whys, Fishbone.
- Applies effective inter-departmental communication and escalation.
- Owns tooling and process from a manufacturability standpoint from development to production release.
- Partners with the Quality department on investigations and corrective actions.
Competencies
- Ability to read, write, speak and understand the English language
- Ability to communicate clearly by conveying and receiving ideas, information, and direction effectively
- Ability to demonstrate adequate job knowledge to deliver a world-class performance
- Ability to challenge oneself to consistently meet all goals and deadlines
- Willingness to strive for excellence by producing work that is free of errors and mistakes
- Desire to delight both customers and coworkers by offering encouragement, fostering teamwork and addressing conflict appropriately
- Commitment to making improvements company-wide
- Demonstrated competence using Microsoft Office
- Use of statistical analysis software
- Interpersonal skills and good communication technique
- Ability to coordinate multiple projects and deadlines, manage and identify the scope
- Act as a project leader on major projects
- Lean Manufacturing- Proficient in the use of problem-solving tools such as 5 why, Fishbone, 8D, etc.
- Understanding of manufacturing processes for medical components and devices.
- Good understanding of metrology principles and methods.
Education and Experience:
Required:
- 4-year degree in Engineering or a related discipline
Salary Range:
$85,000-$100,000 DOE