Consultant Title: Validation Engineer
Duration: 3-6 Months
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).
Medical device manufacturing is highly preferred.
Professional, responsible, energetic and accountable.
SRG ED&I and EEO Statement
• ED&I: Impellam Group and its brands are equal opportunity employers committed to diversity and inclusion.
• EEO Statement: Impellam Group is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.
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