Avispa Technology
Systems Engineer - Assay Development
Avispa Technology, Tucson, Arizona, United States, 85718
Systems Engineer - Assay Development
ROCGJP00039030
Hourly pay:
$40-$45/hr
Worksite: Leading biotechnology company (Tucson, AZ 85755 - Hybrid, Must be 3+ days in office)
W2 Employment,
Group Medical, Dental, Vision, Life,
Retirement Savings Program,
PSL
40 hours/week, 11 Month Assignment
A leading biotechnology company is seeking a
Systems Engineer - Assay Development . The successful candidate will drive requirements definition, risk management, and verification & validation practices in projects.
Responsibilities:
Define requirements, design system architectures, and implement solutions to meet IVD standards.
Take ownership of project deliverables and facilitate the decision-making process with well-considered tradeoffs.
Qualifications:
3-5 years of experience.
Bachelor’s degree in Engineering.
Writing experience in a regulated industry (medical device industry preferred).
Risk analysis (FMEA) work in an engineering discipline (regulated medical device company preferred).
Demonstrated knowledge of systems engineering principles, specifically in requirements engineering, tradeoff analysis, risk management, configuration management, and verification and validation.
Ability to work cross-functionally with many stakeholders, weighing the needs of many stakeholders and coming to an alignment, balancing all needs and tradeoffs.
Assay development experience, particularly with cytology specimens, is preferred.
Prior experience in RETINA (Requirements & Test Integration Application) and with LucidSpark/LucidChart is preferred.
Excellent organizational skills, with the ability to efficiently evaluate, prioritize, and handle multiple projects and priorities is preferred.
Shift:
Monday to Friday, 8 am to 5 pm.
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ROCGJP00039030
Hourly pay:
$40-$45/hr
Worksite: Leading biotechnology company (Tucson, AZ 85755 - Hybrid, Must be 3+ days in office)
W2 Employment,
Group Medical, Dental, Vision, Life,
Retirement Savings Program,
PSL
40 hours/week, 11 Month Assignment
A leading biotechnology company is seeking a
Systems Engineer - Assay Development . The successful candidate will drive requirements definition, risk management, and verification & validation practices in projects.
Responsibilities:
Define requirements, design system architectures, and implement solutions to meet IVD standards.
Take ownership of project deliverables and facilitate the decision-making process with well-considered tradeoffs.
Qualifications:
3-5 years of experience.
Bachelor’s degree in Engineering.
Writing experience in a regulated industry (medical device industry preferred).
Risk analysis (FMEA) work in an engineering discipline (regulated medical device company preferred).
Demonstrated knowledge of systems engineering principles, specifically in requirements engineering, tradeoff analysis, risk management, configuration management, and verification and validation.
Ability to work cross-functionally with many stakeholders, weighing the needs of many stakeholders and coming to an alignment, balancing all needs and tradeoffs.
Assay development experience, particularly with cytology specimens, is preferred.
Prior experience in RETINA (Requirements & Test Integration Application) and with LucidSpark/LucidChart is preferred.
Excellent organizational skills, with the ability to efficiently evaluate, prioritize, and handle multiple projects and priorities is preferred.
Shift:
Monday to Friday, 8 am to 5 pm.
#J-18808-Ljbffr