Medical Device Quality Engineer

1 month ago

Jacksonville, United States Compliance Group Inc Full time

Job Title: Sr Medical Device Quality Engineer

Job Location: Jacksonville, Florida (Fully onsite)

Type: W2 contract


Must have:

Strong Risk Management Experience (Experience in Risk Documentation: Write, review, approve of Riks Management files, RPM calculations, Risk Mitigations, etc.).

Bachelor’s degree in engineering, Science or Technical field.

Minimum of 4+ years of work in the medical device industry experience in Engineering and Quality OR Advanced degree in Engineering, Science or technical field with 2+ years of work in the medical device industry experience in Engineering and Quality with Strong Experience in Validation/Qualification activities: (Write, coordinate, execute, create reports, IQ, OQ, PQ, MVPR, Sampling size determination: For Attribute or variable data, Strong statistical background, etc)

Able to work with a minimum of supervision in a hybrid working organization setup.

Good writing and documentation skills.

Good organizational and verbal communication skills.

Ability to work in a fast-track schedule and meet deliveries on time.

Ability to communicate effectively.

Ability to interact with a very diverse team keeping high ethics standards.


Below The Nice To Have:

ASQ Quality Engineer Certification.

Bilingual English/Spanish preferred but not required.

DMAIC Lean / Six Sigma Certification.

Manufacturing experience within a controlled and regulated industry.

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