Sr Microbiologiste-Sterili Supv

Medtronic plc; Tijuana; Híbrido; MXN 900.000 - 1.200.000; Jornada completa

Descripción de la vacante

Medtronic plc recherche un Sr Microbiologiste-Sterili Supv sur site à Tijuana pour diriger le programme d’assurance stérile et coordonner les activités de microbiologie et de contrôle environnemental. Vous superviserez une équipe et soutiendrez les transferts produits et les audits qualité.

Le poste exige une solide expérience en stérilisation, microbiologie et maîtrise des standards ISO et CFR. Anglais avancé et capacité à diriger des projets d’amélioration continue sont essentiels.

Formación

• Expérience d’au moins 8 ans dans les domaines de la stérilisation et de la microbiologie.
• Connaissance des méthodes d’EO, de radiation et des tests biologiques.
• Maîtrise des standards internationaux liés à la stérilisation et à la microbiologie.

Responsabilidades

• Diriger le programme d’assurance de la stérilité et les activités associées (qualification EO, audits de dose).
• Conduire des transferts et des validations de nouveaux produits en tant que représentant microbiologie et stérilisation.
• Gérer les non-conformances, CAPAs et les rapports de performance qualité.
• Maintenir les documents et soutenir les audits internes et externes liés à l’environnement du contrôle qualité.

Conocimientos

Sterilization

Microbiology

English proficiency

Educación

Bachelor’s Degree in Biological sciences

Descripción del empleo

## Sr Microbiologiste-Sterili SupvPostuler: Sur site: Tijuana, Baja California, Mexico: Temps plein: Offre publiée hier: R78362Chez Medtronic, vous pouvez entamer une longue carrière d’exploration et d’innovation tout en aidant à soutenir l’accès aux soins de santé et l’équité pour tous. Vous dirigerez avec détermination en surmontant les obstacles à l’innovation dans un monde davantage connecté et compatissant.**Journée type**Experienced professional in sterility assurance, microbiology, and environmental control, with expertise in contamination control, sterilization validation, and cleanroom operations. Focused on compliance, product quality, and continuous improvement. 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.* Coordinate the sterility assurance program by leading and supporting EO cycle qualification and requalification, radiation dose audits, EO and radiation annual reviews, and other special testing activities, such as comparative resistance studies and ethylene oxide residual testing.* Lead and support new product transfers and introductions as the sterilization and microbiology representative.* Conduct sterilization and microbiology impact assessments for product or packaging changes.* Coordinate and support product release activities related to sterilization.* Coordinate the bioburden and LAL programs to ensure control, verification, and maintenance of product families.* Develop in-house microbiology and environmental testing techniques and coordinate activities with external laboratories.· Support environmental control activities for cleanrooms and critical facility systems.* Maintain risk management files related to sterilization, environmental control, and microbiology.* Generate, investigate, and follow up on nonconformances and CAPAs related to sterilization, microbiology, and environmental control.· Maintain trend analysis for processed loads, product damage during transit or at sterilizer plants, and sterilization process failures, and prepare associated reports.* Review and update documentation related to sterilization processes, environmental control, and microbiology.* Support internal and external audits related to environmental control, microbiology, and sterilization.* Support regulatory submissions related to environmental control, microbiology, and sterilization.* Lead or participate on projects in alignment with company optimization strategies·* Notify actions, unsafe conditions and environmental risks observations in any of the areas of the plant.* Manage a team of technicians and/or engineers by assigning and monitoring tasks, providing ongoing coaching and feedback, and evaluating performance **PEOPLE MANAGEMENT FUNCTIONAL CAREER STREAM:**Management and supervisory professionals with one or more employees who are focused on tactical, operational and some strategic activities within a specified area. Levels within the management career stream typically have six or more direct reports. The majority of time is spent overseeing their area of responsibility, managing performance, developing talent, engagement and inclusion, communicating business and operational developments, planning, prioritizing and / or directing the responsibilities of direct reports. Goal achievement is typically accomplished through performance of direct and / or indirect reports. A key responsibility of roles in this career stream is managing people. which includes: accountability for mentoring, developing and coaching staff on meeting/exceeding performance expectations and defined objectives, providing leadership to staff ensuring the prioritization of strategic and department level initiatives to include defining performance goals and targets, conducting performance reviews, and staff 1:1s to guide performance management and employee development efforts and manage toward departmental goals.**DIFFERENTIATING FACTORS****Autonomy:**Supervises team members or subordinate supervisors, providing tactical and / or technical leadership. May perform ongoing operational tasks. Receives assignments in task-oriented terms and delivers results according to established procedures.**Organizational Impact:**Plans and establishes goals and objectives for a team, typically within (1) department. Decisions impact project or department schedules, customer satisfaction levels, or allocation of time or material resources. Typically does not have budget or P&L accountability, but may manage day-to-day elements of the budget (eg, overtime for staff).**Innovation and Complexity:**Makes improvements to processes, systems or products. Problems and issues faced are difficult and may require understanding of broader set of issues, including multiple job areas or specialties.**Communication and Influence:**Communicates with internal and external customers and vendors, across various levels of the organization. Shares and exchanges relevant information to reach solutions, and gaining cooperation of other parties .**Leadership and Talent Management:**May be a second level supervisor of employees in the Support career stream, such as production, distribution or technicians . May be a first level supervisor of employees in the Associate or Intermediate level in the Specialist career stream . May be a first level supervisor of employees at level IV and V in the Support career stream . Leads, directs and reviews the work of team members in order to accomplish operational plans and results. Provides primary input to hiring, firing, promotion, performance and rewards decisions for direct reports.**Required Knowledge and Experience:*** Bachelor’s Degree in Biological sciences or chemical engineering* Experience for at least 8 years in Sterilization and Microbiology area* Experience in Principles of Ethylene Oxide, Radiation (GAMMA, Ebeam) sterilization method.* Experience in Microbiology Principles for Product sterility, Bioburden Testing, Bacterial Endotoxin.* Advanced English Level* Knowledge of international standards related to sterilization, microbiology and environmental control (ISO 11135, ISO 11137, ISO 11737, ISO 10993, AAMI TIR28, ISO 14644, ISO 14698, ISO 17025, ANSI /AMMI ST72, CFR 21 part 58 and USP chapters 1116 and 1117.* Knowledge of Medical Device Quality system (ISO 13485)* Knowledge of Root cause analysis (Five Whys, Fishbone Diagram (Ishikawa), FMEA) Good Manufacturing practices and good documentation practices.