Senior Design Verification Engineer

Job Title: Senior Design Verification Engineer

Pay Rate: $58 to $63.05/HR

Duration: 9 months

Location: Irvine, CA

Our Client is a Global medical device Manufacturer.

We are looking for a Senior Design Verification Engineer.

• Create, test, and/or improve products by developing 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 models and drawings/prototypes, etc., to establish/characterize product and/or process specifications
• Create/update more complex design control documents including requirement specs, and risk documents (Design requirements document DRD, design verifications plan, DFMEA, technical summaries, alignment of design documents with risk control documents such as Risk management worksheet or AFMEA/PFMEA)
• Develop and execute engineering project plans (design verification Plan)
• Identify, evaluate, manage, and provide guidance to suppliers, including establishing tolerances and defining acceptance criteria for suppliers
• Assign R&D support tasks; give instruction to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work
• Evaluate input and form a technical recommendation including designing parts, components, and subsystems
• Train, coach, and guide lower-level employees on routine procedures
• Other duties assigned by Leadership

Requirements:

• Bachelor's Degree in Engineering with a preference for Mechanical Engineering plus 4 years experience Required or Master's Degree or equivalent in Engineering or Scientific field, 3 years experience Required or Ph.D. or equivalent in Engineering or Scientific field Required.

Additional Skills:

• Proven expertise in usage of MS Office Suite; PTC Creo for CAD required
• Windchill for product life cycle management ( design control elements such as Design requirement documents, drawings, and risk control documents)
• Strong 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)
• Substantial understanding and knowledge of principles, theories, and concepts relevant to Engineering
• Strong problem-solving, organizational, analytical, and critical thinking skills
• Substantial understanding of processes and equipment used in assigned work
• Good leadership skills and ability to influence change
• Knowledge of and adherence to our 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 inter-departmental teams and key contacts representing the organization on contracts or projects
• Ability to interact with senior internal and external personnel on significant matters often requiring coordination between organizations
• 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 the environment and prevention of pollution under their span of influence/control