Quality Validation Engineer - Apidel Technologies

Job Description
Quality Site Validation Engineer - ONSITE - HOLDREGE, NE

NEW UPDATE!!- - HM IS NOW ACCEPTING CANDIDATES THAT ARE CURRENTLY LOCATED OUTSIDE OF THE HOLDREGE, NE AREA, BUT CANDIDATES MUST UNDERSTAND THAT THEY WILL NEED TO RELOCATE & MOVE TO HOLDREGE ON THEIR DOLLAR FOR THE 2-YEAR CONTRACT. RELOCATION IS NOT PROVIDED. LOCAL CANDIDATES SUBMITTED WILL BE PRIORITIZED & REVIEWED FIRST. PLEASE REVIEW THE HOURLY PAYRATE FOR THE CANDIDATE\'S RATE. (

Position Details:
Request: CONTRACT ONLY - However,  would consider conversion after worker proves qualifications & skill set
Targeted Start Date: November 3rd 2024
Shift: 1st Shift
Hours Per Week: 40
OT: Yes, if approved by manager.
Type: ONSITE ONLY
Location: Holdrege, NE
HM: Shelley Hendricksen

Contract Length - Approximately 2 years
Interview Process:
Onsite Interview & Tour (Typically they will just do 1 visit for interview & tour, but they may do a second)

Pre-Hire Requirements:
Pre-Hire Drug Screen: YES
B/C: YES (JG 3 Plus)
Physical / Lifting Assessment: NO
Requirements:
EDUCATION
B.S. degree Required.
B.S. degree in Engineering (Industrial, Mechanic) Desired
EXPERIENCE
3%2B Years Quality experience including Validation and Quality Engineering responsibilities.
Demonstrate success with statistical and problem-solving methodologies.
Excellent knowledge of the principles for Quality Engineering and Quality management as related to validation process on medical devices.
Strong understanding of failure analysis, test methods and engineering tolerances.
Strong verbal, written and interpersonal skills.
Proficient with Minitab or other statistical software, MS Word, Excel, and MS project.
Six Sigma Certification Desired:
ASQ CQE
Working knowledge of 21CFR820, ISO 13485.
NOTE
Medical Industry Experience Needed. No job hopping or unjustified gaps in employment. Resumes should be 3 pages max.
Please Review JD and Worker Request Form Attached