Edwards Lifesciences Corp

2nd Shift Engineer II, Manufacturing

Edwards Lifesciences Corp • $75K — $95K *
Salt Lake City, UT 84118In-Person
Manufacturing & Automotive
Less than 5 years of experience
2 days ago
Be an Early Applicant
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Engineering or Scientific field with 2 years experience, or a Master's Degree with relevant internship or thesis experience
  • Solid understanding of engineering principles and concepts
  • Experience with regulatory requirements in the medical device industry preferred
  • Proficient in MS Office Suite, MS Project, and CAD
  • Strong problem-solving and analytical skills

Responsibilities

  • Optimize manufacturing processes using engineering methods for continuous improvement
  • Develop and execute experiments and tests to validate manufacturing processes
  • Analyze and resolve manufacturing and compliance issues effectively
  • Create training and documentation materials to facilitate knowledge transfer
  • Establish project plans to meet customer expectations using project management tools
  • Oversee and instruct technicians in conducting tests and coordinating work

Benefits

  • Professional development opportunities
  • Collaborative work environment
  • Health and wellness programs
  • Flexible work hours
  • Access to cutting-edge technologies
Full Job Description
How you'll make an impact:
  • Optimize manufacturing processes, including using engineering methods (e.g., SIX Sigma and LEAN methods) for continuous process improvement and/or re-design/design of equipment, tools, fixtures, etc. to improve manufacturing processes, employing technical design skills
  • Develop moderately complex experiments and tests (including writing and executing protocols) to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports
  • Analyze and resolve moderately complex Manufacturing and Compliance issues (e.g., CAPA, non-conformances, audit observations)
  • Develop training and documentation materials (e.g., work instructions) for production to enable the seamless knowledge transfer of project and manufacturing processes
  • Establish project plans to ensure deliverables are completed to customer's expectations, using project management tools (e.g., Project Plan, Risk Analysis, etc.)
  • Oversee manufacturing support tasks; give instruction to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work
  • Other incidental duties assigned by Leadership


What you'll need (Required):
  • Bachelor's Degree in Engineering or Scientific field with 2 years experience OR
  • Master's Degree or equivalent with internship, senior projects, or thesis in Engineering or Scientific field including either industry or industry/education


What else we look for (Preferred):
  • Experience working in a regulated industry, medical device preferred
  • Good computer skills in usage of MS Office Suite including MS Project; CAD experience
  • Good documentation, communication (e.g., written and verbal) and interpersonal relationship skills including consultative and relationship management skills
  • Basic understanding of statistical techniques
  • Previous experience working with lab/industrial equipment
  • Solid understanding and knowledge of principles, theories, and concepts relevant to Engineering
  • Solid problem-solving, organizational, analytical and critical thinking skills
  • Solid understanding of processes and equipment used in assigned work
  • 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 applicable FDA regulations for medical device industry
  • Strict attention to detail
  • Ability to interact professionally with all organizational levels
  • Ability to manage competing priorities in a fast paced environment
  • Must be able to work in a team environment, including the ability to manage vendors and project stakeholders
  • 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

About Edwards Lifesciences Corp

Edwards Lifesciences is an American medical technology company headquartered in Irvine, California, specializing in artificial heart valves and hemodynamic monitoring. It developed the SAPIEN transcatheter aortic heart valve made of cow tissue within a balloon-expandable, cobalt-chromium frame, deployed via catheter. The company has manufacturing facilities at the Irvine headquarters, as well as in Draper, Utah; Costa Rica; the Dominican Republic; Puerto Rico; and Singapore; and is building a new facility due to be completed in 2021 in Limerick, Ireland.
Learn more about Edwards Lifesciences Corp
Size
15,700 employees
Market Cap
$45.6 billion
Industry
Pharmaceuticals & Biotech
Net Income
$823.4 million
Founded
1958
5 Year Trend
+12%
Revenue
$4.3 billion
NASDAQ
EW
* Ladders Estimates

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