Sobre este puesto de Sterilization Engineer II en Medtronic
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in the Life
The Sterilization Engineer II is responsible for ensuring that sterilization processes—particularly Ethylene Oxide (EO)—are compliant with regulatory and internal quality system requirements, including FDA, PMDA, ISO 11135, and ISO 13485 standards.
S/He will lead sterilization validations, process improvements, and global standardization initiatives.
Responsibilities may include the following and other duties may be assigned.
Ensure sterilization processes including sterilization release and validation complies with specifications and all relevant FDA regulations and ISO standards, such as ISO 11135, ISO 13485.
Validate and implement sterilization processes and microbiological controls.
Navigate within the QMS to create and release documents and procedures, including validation protocols/reports, routine release documentation, and procedural updates.
Creates & executes validation documentation with full stakeholder alignment covering product scope, resistance hierarchy, process equivalency, performance qualifications, etc.
Works with product/packaging stakeholders to evaluate product limitations & determine EO sterilization processing bounds.
Collaborate with global teams to align strategy, planning and execution of sterilization processes, protocols, and best practices.
Oversee the requalification, maintenance and calibration of sterilization equipment to ensure optimal performance.
Provide technical support to manufacturing operations, including root cause analysis, CAPA implementation, and training.
Drive and participate in continuous improvement initiatives related to sterilization effectiveness, efficiency, and compliance.
Maintain and update sterilization-related risk assessments (e.g., FMEAs).
Support or lead investigations and corrective/preventive actions (CAPAs) related to sterilization.
Actively participate in internal and inter-facility audits to assess compliance and process robustness.
Perform additional responsibilities or project assignments as directed by the Manager or Supervisor.
Attributes
Demonstrates high ethical standards and integrity in all actions and decisions.
Flexible and adaptable to changing priorities, challenges, and environments.
Strong team player, including cross-functional teams, with a collaborative mindset
Meticulous attention to detail and commitment to quality.
Provides technical guidance and mentorship to less experienced engineers
Excellent problem-solving skills.
Proven project management and interpersonal skills.
Excellent organizational and judgment skills.
Required Knowledge and Experience:
Bachelor’s degree in engineering (Microbiology, Biotechnology, etc.) or equivalent
Advanced degree (e.g., Master’s) is a plus and may reduce experience requirements.
Relevant certifications in sterilization or quality systems are advantageous.
Minimum of 2 years of experience in medical device or pharmaceutical industry, preferably within Sterility Assurance; or a minimum of 0 years of relevant experience with an advanced degree (Master’s or higher)
Experience and knowledge of applicable standards and regulations (e.g., ISO 11135, ISO 13485, FDA, PMDA).
Direct experience with EO sterilization equipment, process controls & change management. Experience with parametric release processing.
Knowledge in microbiological testing includes bioburden, endotoxin, EO residual testing and cleanroom control is advantageous.
Proficiency in written and spoken English. Strong communication and interpersonal skills; able to clearly articulate technical concepts across all levels of the organization
Computer proficiency using word, spreadsheet, Minitab.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
About Medtronic
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here