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Systems Integration Manager

Oncocyte Corporation
Irvine, CA Full Time
POSTED ON 1/12/2025 CLOSED ON 1/22/2025

What are the responsibilities and job description for the Systems Integration Manager position at Oncocyte Corporation?

Job Details

Job Description

Job Description

Who we are:

Oncocyte is a precision diagnostics company with a mission to improve patient outcomes by providing personalized insights that inform critical decisions throughout the patient care journey.

Mission of the role:

The Systems Integration Manager will be a key member of the team responsible for defining product strategy, scope, and launch decisions for IVD products. This role will be responsible for ensuring a seamless integration of the IVD products from a system level through collaboration with internal and external stakeholders. The role will work cross-functionally to ensure the appropriate commercial, technical, regulatory, manufacturing, and logistics resources are available to support the successful execution of product strategy in IVD markets.

Your day-to-day:

  • Work with a team of subject matter experts internally and externally from diverse fields to support OCX s diagnostics product portfolio from concept through development, verification and validation, design transfer, manufacturing, and commercialization
  • Lead the definition and management of requirements and characterization of the systems/devices
  • Define, plan, and coordinate formal technical design reviews
  • Lead and complete system integration across multi-functional subject areas
  • Lead risk management and hazard analysis activities
  • Lead FMEA document generation in design, process, user error, and software
  • Maintain system traceability matrix
  • Support failure mode analysis and troubleshooting
  • Coordinate with external vendors and CMOs to maintain production timeline and logistics
  • Support in the design transfer to manufacturing
  • Coordinate with external partners and consultants to ensure proper IVD SW development and V&V under FDA QMS and ISO13485 guidance
  • Write system-related documents such as SOPs, QC, and IQ/OQ/PQ under the IVD product lifecycle
  • Support the regulatory submissions, product labeling, and complex submissions issues
  • Undertake other leadership and strategic tasks as assigned to support the organization's objectives. These may include cross-functional collaboration, process improvement initiatives, and addressing emerging business needs requiring managerial oversight.

What it takes to do this job:

  • MS or above in engineering, biological science, physics, or chemistry
  • 5 years of system-level integration and validation experience with a strong understanding of medical device design controls and change controls
  • Proficient with Design Controls and Risk Management
  • A significant contributor to IVD product development, delivered at least one project that was successfully launched under the US FDA or CE mark regulatory regime
  • Experience mentoring and leading teams of technical contributors
  • Ability to comprehend principles of engineering, physiology, and medical device use
  • Knowledge of a wide range of disciplines in systems integration, including molecular biology and biochemistry, statistics, use of computers, and other analytic methods to solve problems in medical device development
  • Basic molecular biology wet lab experience - including methods such as - sample extraction/preparation, dPCR, qPCR, or NGS is preferred
  • Familiarity with QMS, 21 CFR 820, and ISO 13485 that supports medical device products for FDA and CE marking applications
  • Software V&V protocol/experience is a plus

Who you are:

  • You have a do what it takes no job is too small team player and a positive attitude with a willingness to wear other hats and step in to perform and support other roles when needed.
  • You have superb written and verbal skills and an exceptional ability to communicate clearly and professionally.
  • Your organizational skills, attention to detail, and ability to multi-task are excellent.
  • You like building effective internal and partner relationships including with team members, clients, vendors, and suppliers.

You will have the opportunity to:

  • Improve patient outcomes.
  • Meaningfully impact the company s short-term and long-term success.
  • Work collaboratively across all levels within the organization.
  • Grow your role as you see fit.
  • Learn everything there is to know about diagnostic laboratories.
  • Create an inspiring workplace.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
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