Ing. Esterilización Jr (12 Meses) (Tijuana)

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

Responsibilities may include the following and other duties may be assigned.

• Work independently with guidance and direction from senior members of the team and manager.
• Provide understanding of the audit process including types of audits, planning, preparation, execution and follow‑up.
• Perform, coordinate, execute and summarize sterilization requalification (EO, radiation, steam and chemical sterilization).
• Work with little guidance to maintain sterilization processes, certifications and procedures for the sterilization operations.
• Support internal and external audits.
• Review engineering change orders and define microbiology or sterilization risks.
• Support in the resolution of non‑conformances and implement corrective action.
• Work with facility maintenance and other departments for any Sterilizer and CEA improvement/corrective activities.
• Participate in special projects as assigned.
• Reviews change control notifications for impact to sterilization/microbial testing.
• Assuring that the Microbiology / Sterilization function is maintained per industry standards.

Additional Responsibilities

Responsibilities may include the following and other duties may be assigned.

• Analyzes chemical, biological or microbiological products, raw materials, in‑process materials, release test samples or stability samples in support of the company’s quality program.
• Prepares, cleans, disinfects, and/or sterilizes instruments, materials, products, and/or supplies.
• Follows protocols and regulations in order to clean, store, and/or deliver products, supplies, and/or instruments.
• Interprets and evaluates the analyses in terms of accuracy and precision compared against established specifications and recommends and implements corrective action where necessary.
• Develops, validates, and implements controlled environment methods.
• Applies existing techniques and procedures with recommendations and implementation of modification for improved efficiency, or devises and develops new analytical methods and techniques.
• Performs qualitative tests or quantitative assays on samples using techniques that vary from use of standard analytical equipment to highly modern and automated instrumentation.
• May also be involved in establishing requirements for the transfer of methodology from R&D.

Technical Specialist Career Stream

An individual contributor with responsibility in our technical functions to advance existing technology or introduce new technology and therapies. Formulates, delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering R&D, systems or initiatives related to new technologies or therapies - from design to implementation - while adhering to policies, using specialized knowledge and skills.

Differentiating Factors

• Autonomy: Entry‑level individual contributor on a project or work team. Works with close supervision.
• Organizational Impact: Delivers work of limited scope, typically smaller, less complex projects or related activities.
• Innovation and Complexity: Identifies, defines and addresses problems that are not immediately evident but typically not difficult or complex. Makes minor changes in systems and processes to solve problems.
• Communication and Influence: Communicates primarily with internal contacts within immediate group. Contacts others to gather, confirm and convey information.
• Leadership and Talent Management: N / A - job at this level is focused on self‑development.

Required Knowledge and Experience

• Bachelor's degree
• 0–2 years of engineering experience in manufacturing or sterilization, preferably in a regulated industry (medical devices, pharmaceuticals, biotechnology, or similar).
• Basic experience in manufacturing, sterilization, or laboratory processes.
• Experience participating in change control processes, including reviewing technical documentation and coordinating with functional areas.
• Ability to analyze and understand complex technical reports, including process validation reports.
• Experience reviewing or supporting activities related to process validations, technical documentation, or process engineering is desirable.
• Ability to work independently, researching technical and regulatory information as needed.
• Effective communication skills in both English and Spanish, written and verbal, for interaction with general teams and reviewing technical documentation.

Nice to have

• Basic knowledge of sterilization processes (Ethylene Oxide)
• Familiarity with environments regulated under GMP, FDA, or ISO 13485.
• Ability to analyze data and reso