The Sr Sterilization Validations engineer will:

• The Sr Sterilization Validations engineer eventually will work with a significant degree of independence and self-direction to ensure the developing, implementing, and executing validation related programs in compliance with
• CENTERPIECE’s QMS and compliant to 21 CFR Section 820, EN ISO 13485, ISO 11135, Environmental Standards, and other as necessary operating requirements.
• The Sr Sterilization Validations engineer will work closely with the operations and quality teams to ensure the adherence to validations projects (budgetary, timeline, etc).
• Generate validation IQ/OQ/PQ protocols, risk assessments, reports, and technical files.
• This position will routinely interact with the production operations team.
• Review risk assessments, commissioning protocols.
• Proven technical experience with demonstrated success in working in a team environment to successfully achieve corporat...