Senior Design QA Engineer
ThermoFisher Scientific
Austin, TX (In Person)
$97,200 Salary, Full-Time
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Job Description
- Work Schedule
- Standard (Mon-Fri)
- Environmental Conditions
- Office
- Job Description
- As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale.
- Discover Impactful Work
- In this role, you will lead all aspects of the "end to end" design control and new product development lifecycle as a quality core team lead for New Product Introductions (NPIs) for Companion Diagnostics (CDx). You will ensure that products are designed, developed, and validated in compliance with regulatory requirements and internal quality standards.
- Location
- This is a fully onsite role based in either of the 3 locations: Austin, TX; Carlsbad, CA; Frederick, MD. Please note that relocation assistance is not provided.
- A Day in the Life
- + Work with multiple teams to lead and support design control activities across the full product development lifecycle for CDx NPIs including: + User and Product Requirements + Design Verification and Validation (V&V) + Risk Management + Design Reviews + Ensure activities are conducted in compliance with all applicable regulatory requirements, international standards, and internal procedures + Establish, maintain, and drive quality standards while supporting a culture of continuous improvement and compliance + Participate in team projects and assignments, facilitating or leading sub-teams as necessary •Keys to Success•Education•+ Bachelor's degree in Engineering or Science field (Chemistry, Microbiology, Genetics, Biochemistry, or related) •Experience•+ 4+ years of experience in Quality Assurance (Quality Engineering, QA, QC, Supplier Quality, or NPI) + 4+ years of QA experience in a regulated industry (pharmaceutical, medical device, or biotech) preferred + Demonstrated understanding of product development lifecycles, design change and change control, product validation methodologies, and manufacturing/product process control methodologies + Experience with companion diagnostics (CDx) and clinical integration is a plus •
Knowledge, Skills, Abilities:
- + Strong knowledge of c
GMP, ISO 13485/14971, IEC 62366, EU
IVDR, and applicable regulatory requirements (FDA, EMA, etc.) + Proficiency with quality management systems and MS Office tools + Strong analytical, problem-solving, and troubleshooting skills + Excellent communication and interpersonal skills + Ability to work independently and collaboratively + Strong attention to detail with the ability to maintain a broad perspectiveOther:
- + Must be legally authorized to work in the United States without sponsorship now or in the future + Must be able to pass a comprehensive background check and drug screen
- Compensation and Benefits
- The salary range estimated for this position based in Maryland is $83,300.
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