• Irvine, CA - will be on-site full time
• 1 year contract with potential to extend/convert to FTE based on performance and business
• Target PR: 40-44/hr
• Benefits: Medical, Dental, Vision insurance, 401k match, etc.
• Schedule: Standard office hours, potential of overtime but not likely to exceed 5 hours.

Must haves for this position:

• Prior experience as a sustaining engineer (R&D) in a medically regulated industry
• Design verification and validation experience in the medical device industry
• Exposure to failure mode analysis.
• PPK, MLTL, or any base level knowledge of statistical tools or analysis (Minitab use).
• Test method validation
• Design verification (plans & protocols), reporting, and testing
• Data failure analysis on the design verification testing
• 3 plus years of relevant work experience with a Bachelor's, Master's preferred

Summary:

Applies knowledge of technical principles and systems/procedures to maintain and optimize CC legacy products.

Job Responsibilities:

• Test, and/or improve products by developing moderately complex experiments and tests (including writing and executing protocols), analyze results, make recommendations, and develop reports, based on engineering principles
• Generate work instructions, test methods, engineering drawings/prototypes, etc. to establish/ characterize product and/or process specifications
• Create/update portions of design control documents including requirement specs and risk documents
• Assign R&D support tasks; gives instruction to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work
• Identify, evaluate, manage, and provide guidance to suppliers, including establishing tolerances and defining acceptance criteria for suppliers
• Other duties assigned by Leadership

Skills :

• Good computer skills in usage of MS Office Suite; CAD experience preferred
• 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 required (if applicable)
• 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 Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
• 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
• Ability to build productive internal/external working relationships
• 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

Education/Experience:

• Bachelor's degree in engineering required.
• 2-4 years experience required.

This position is suited for Sustaining Engineers or R&D Engineers. Those with Manufacturing or Quality engineer backgrounds wouldn't be considered. This manager also won't consider candidates with less than 3 years or experience or without a medical device background.

Job #610208