STERIS

Scientist I

$60K–$75KFull-time · Minneapolis, MN
✓ Verified live on the employer's own system · added 4 days ago
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Requirements

Education: Bachelor's degree

Skills & tools

SterilizationMaintenanceManagementTeam LeadershipStatistical AnalysisRecordkeepingSafety MeetingsProcess Improvement

Benefits — mentioned in this posting

Paid time off401(k) / retirementHealth, dental & visionFamily / parental leaveWellness & perks
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Full job description

Position Summary

The Scientist I is responsible for the activities related to validation of sterilization processes across STERIS operating facilities. Activities include calibration of data collection systems, operation, and data collection related to portable temperature/humidity sensors; coordinating with external laboratories for equipment calibrations and maintenance; coordinating with Customers for test sample processing and requalification studies; coordination and proper handling of product samples for transfer to outside laboratories for testing; and other routine tasks as directed by the immediate supervisor or manager.

Expected schedule is Mon - Fri with the potential for after-hours and/or weekend work per project needs.

What You'll do as a 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 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.
  • Ethylene Oxide specific:
  • Provides critical support for Customer turnkey validation service(s) by executing and assisting in the management of the validation activities, such as coordination of samples receipt, placement, retrieval,
  • storage and shipment, generation and maintenance of documentation for study activites.
  • Works with Customers during Customer driven studies to coordinate handling of material resources for use in studies, such as dunnage loads and remote sensor availability.
  • 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.

Pay range for this opportunity is $60,000 - $75,000. This position is eligible for bonus participation.

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This posting was published by STERIS on their own careers system and is shown here with a direct link to apply there. Employers: for corrections or removal, contact jobs@veritahire.com.