Day to day responsibilities:

Working closely with regulatory agencies, including the FDA.

Work closely with internal stakeholders including quality, regulatory, clinical, technical services, and production.

Maintain documentation within the expectation of regulatory standards including (but not limited to).

Requirements:

Medical device manufacturing is highly preferred.

Professional, responsible, energetic, and accountable.

At least 5 years of Validation experience in the Med Device Industry.

Job Type: Contract

Pay: $38.97 - $76.12 per hour

Schedule:

• 8 hour shift

Work Location: Hybrid remote in Swiftwater, PA 18370

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