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Salary
$111k – $206k per year (Estimated)
Location
In office (Draper)
Seniority
Staff · 13+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
Edwards Lifesciences is an American medical device company that became independent from Baxter in 2000 but traces its work to the first commercially available artificial heart valve, developed by Miles Lowell Edwards in the late 1950s. It concentrates entirely on structural heart disease and critical care monitoring, and its transcatheter aortic valve replacement business changed cardiac practice by allowing valves to be delivered through a catheter rather than through open chest surgery. Headquartered in Irvine, California and listed on the New York Stock Exchange, it holds a leading position in a market it largely created.

Innovation starts from the heart. Edwards Lifesciencesis the leading global structural heart innovation company, driven by a passion to improve patient lives.With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Staff Technologist position is a unique career opportunity that could be your next step towards an exciting future.

Provides technical and function-specific knowledge to support Operations and Engineering activities.

Key Responsibilities:

  • Key SME (Subject Matter Expert) with in-depth knowledge and technical proficiency in asset management, equipment maintenance, and manufacturing support activities
  • Design, set-up and execute complex feasibility studies, experiments, and tests - both creating and following established protocols - to develop findings for the validation and improvement of equipment and manufacturing processes/methods based on engineering principles; analyze results, make recommendations, and develop reports for Engineering review
  • Manage all aspects of project management, using such tools as Microsoft Project, Gantt charts, etc., to ensure on-time and on-budget project completion, including interfacing with all parties, allocating resources, negotiating competing priorities, mediating conflicting objectives, and escalating issues as needed for resolution
  • Collaborate with Engineering on systemic root cause investigations for CAPA
  • Review documentation and take appropriate actions to ensure that information is appropriately catalogued and follow through to validation and qualification of equipment, including transferring information to appropriate locations, e.g., ECRs, SOPs, drawings, and tooling, for Engineering approval
  • Lead projects to develop new complex tools/equipment for implementation in multiple areas
  • Design, develop and sustain processes and procedures, including methods to train users
  • Utilize manufacturing software (e.g., JDE, QMS, PLM) to update documentation in systems (e.g., ECRs, Blue Mountain)
  • Provide coaching and guidance to technicians
  • On time arrival to work, regular attendance without excessive absenteeism, and working a full 8 hour or longer work period
  • Other incidental duties (e.g. occasional photo copying or deliveries) Education and Experience: H.S. Diploma or equivalent 15 years' related experience or Associate's degree or equivalent 13 years related experience Required in CNC and micromachining. 15 years previous experience in manufacturing and/or medical device experience Preferred Additional Skills:
  • Excellent written and verbal communication, interpersonal, and relationship building skills with focus on creating presentations, influencing and conveying recommendations
  • Problem solving methodology, root cause analysis, and GDP (Good Documentation Practices)
  • Strong computer skills, including usage of MS Office Suite; and CAD if applicable
  • Extensive knowledge of validation and improvement of automated equipment
  • Ability to troubleshoot manufacturing equipment
  • Knowledge of material compatibility in the proposed use environment
  • Ability to execute the fundamentals of project management
  • Extensive knowledge of routine preventive maintenance of production equipment
  • Extensive knowledge electrical, mechanical, electronic, pneumatic, and controls
  • Knowledge of and adherence to Edwards Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
  • Knowledge of Good Manufacturing and Good Documentation Practices supporting a medical device environment
  • Must be able to work independently in completing complex projects, developing work instructions, and providing guidance to advance the competency of other technicians
  • Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

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