Medical Device Equipment Engineer II — Validation

Grove Technical Resources; Minneapolis (MN); On-site; USD 70,000 - 100,000; Full time

Job summary

Grove Technical Resources is seeking an Equipment Engineer II to support qualification and validation of manufacturing equipment for ENT medical device products. The role is onsite in Minneapolis, MN, with a 12+ month duration and W2 employment.

Candidates should have 3–4 years of experience in equipment engineering, validation, or automation support. Responsibilities include IQ/OQ/PQ, protocol and report writing, and coordination of TMV activities within a regulated medical device environment.

Qualifications

• Experience in equipment engineering, validation, manufacturing, or automation support is required.
• Experience with IQ/OQ/PQ and validation protocols is essential.
• Experience in a regulated medical device environment (FDA/GMP) is required.

Responsibilities

• Support manufacturing equipment qualification and process validation activities for medical device products.
• Coordinate validation activities including test methods and validation reports.
• Assist with change control and CSV activities as applicable.

Skills

Equipment Qualification (IQ) & Tool

Process Validation Lifecycle

Validation Protocol & Report Writing

Manufacturing Equipment & Automation

TMV Coordination

FDA/GMP Environment

CSV (Nice to Have)

Change Control (Nice to Have)

Education

Bachelor's Degree in Engineering or related field

Job description

Grove Technical Resources is seeking an Equipment Engineer II to support qualification and validation of manufacturing equipment for ENT medical device products. The role is onsite in Minneapolis, MN, with a 12+ month duration and W2 employment.

Candidates should have 3–4 years of experience in equipment engineering, validation, or automation support. Responsibilities include IQ/OQ/PQ, protocol and report writing, and coordination of TMV activities within a regulated medical device environment.