Quality Engineers Position Available In Duval, Florida
Tallo's Job Summary: Quality Engineers are responsible for performing hands-on quality engineering tasks in a medical device environment. Requirements include a Bachelor's degree in Engineering, 4+ years of experience in Quality or Supplier Quality, and proficiency in Test Method Validation and Risk Documentation. Preferred skills include ASQ Certification and Lean/Six Sigma. Responsibilities include coordinating validation activities, reviewing quality records, and contributing to risk mitigation strategies. Salary details are in compliance with various Fair Chance Ordinances.
Job Description
Performs hands-on quality engineering tasks across multiple projects supporting validation, test method development, and risk management in a medical device environment.
Job Requirements:
Bachelor�s degree in Engineering (required) Minimum 4+ years experience in Engineering, Quality, or Supplier Quality within the medical device industry Advanced degree with 2+ years of relevant experience accepted Strong experience with Test Method Validation (TMV) and Measurement System Analysis (MSA) Proficient in Risk Documentation, including Design Files, Risk Management files, RPM P1/P2 calculations, and mitigations Strong experience in Validation/Qualification (IQ, OQ, PQ, MVPR, sampling plans, and statistical analysis) Proficient in PPAP documentation and review Capable of performing labor-intensive quality engineering tasks with minimal supervision
Preferred Skills:
Experience with robotics or electronics ASQ Quality Engineer Certification Lean/Six Sigma (DMAIC) Certification Manufacturing experience in a regulated industry Bilingual English/Spanish Prior experience with Medtronic processes or systems
Job Responsibilities:
Execute and coordinate validation and qualification activities across multiple product lines Review and approve quality records related to design, risk, and validation documentation Support multiple active projects simultaneously with hands-on engineering involvement Conduct P1 and P2 calculations and contribute to risk mitigation strategies Maintain documentation aligned with medical device regulatory requirements Collaborate with cross-functional teams in a hybrid or onsite environment as required
Pay Details:
The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance
