Scientist I
- Supports the conduct of scientific studies for investigation and validation purposes.
- Contributes to creating and maintaining valid sterilization processes in the medical device or pharmaceutical industry that comply to FDA regulations, ISO, AAMI, and ASTM standards.
- Acts as liaison between Customer and the facility leadership during Customer driven studies.
- Assists in statistical analysis of data, such as variation analysis, specific to the modality in use.
- Contributes to successful product processing by performing dosimeter calibrations or temperature/humidity sensor calibrations.
- Ensures all internal equipment is calibrated per procedure requirements and coordinates calibrations with external vendors.
- Ensures processes are maintained in a validated state by supporting periodic verifications and execution of revalidations or requalifications following changes.
- Contributes to safe and accurate processing by notifying management of any event, item or documentation that may have a concern in regard to regulatory or specification compliance, Customer product quality, or employee safety.
- Maintains a safe work environment by attending safety meetings with local facility, completing safety rounds, and tracking all hazardous materials as contained in the Safety Data Sheets.
- Communicates in an effective manner by utilizing accepted business practices in a courteous and professional manner providing timely and accurate responses and service oriented offers of assistance.
- Protects company confidential information by properly storing, retrieving and disseminating such information only to those authorized.
- Exhibits a commitment to the AST shared values of Customer Satisfaction and Continuous Improvement through ensuring defect-free workmanship, assisting others to meet the Customer's needs, searching for efficient and effective ways to reduce waste, being active and accountable for Customer satisfaction, and satisfying the Customer's needs with a sense of urgency.
- Contributes in a team effort by performing according to the guidelines outlined in the STERIS Code of Business Conduct, the GMP, Lean principles and other directives; supports the directives and decisions of higher level management and performs other duties as assigned.
- Bachelor's degree in a scientific discipline or related field.
- Experience working in a regulated environment (e.g., GMP, GLP, or similar).
- Strong organizational skills with the ability to manage multiple tasks and priorities effectively.
- Demonstrated proactive approach to task management, ensuring timely completion of individual and team objectives.
- Ability to take initiative and maintain accountability for assigned responsibilities.
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