PMO Sr Analyst

hace 5 días


Ciudad Juarez, México Johnson & Johnson A tiempo completo

At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity.

Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.

When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough. At Johnson & Johnson Medical Devices Companies, we are using our breadth, scale, and experience to reimagine the way healthcare is delivered and to help people live longer, healthier lives. In a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics, and interventional solutions with the big ideas of others to design and deliver doctor and patient-centric products and solutions. We are in this for life. We are changing the trajectory of human health, **YOU CAN TOO.**

**We are searching for the best talent for PMO SR Analyst (Temporary 24 months) to be in Juarez.**

**JOB SUMMARY**

This job description covers the skills & responsibilities for the Sr PMO Analyst position, responsible for:

- Being accountable for maintaining relationships with suppliers & key stakeholder to ensure that EES Supply Chain

G&Os are met.
- Actively participate in the end-to-end JNJ EES Supply Chain PMO team focused on driving efficiency, operational

capability, and other sources of supply chain improvements across the broader organization.
- Support end to end EES Program Manager in developing and managing the portfolio of Supply Chain strategic

projects to drive Quality, Growth, Delivery and Cost improvements globally across the EES Supply Chain

organization.
- Establish, collect, analyze, and present monthly and/or quarterly metrics and facilitate scorecard reviews

including risk management and corrective action processes and tracking of action plans Implement standard

best practices for project management, measurement, and prioritization.
- Establish and facilitate governance forums including establishing the appropriate cadence, timing, agendas,

participants, tracking and documentation of actions plans. Leading, coordinating and facilitating execution of all

critical paths of the E2E Supply Chain.
- Anticipating issues and delivering critical projects solutions for E2E supply interruptions, alternative material

solutions and mitigations to accelerate the flow of critical products, reduce customer impact.
- Prepare reports, purchase orders, supporting all administrative functions. Coordinate credo survey logistics.

Comply with safety policies and procedures.

**DUTIES & RESPONSIBILITIES**
- Conducts studies, performs research, and prepares reports.
- Administrate purchase orders.
- Ensures compliance with rules and regulations.
- Responsible for supporting all administrative functions for operations department.
- Experience to include but not limited to, presentations, meetings, and events coordination, etc.
- Must coordinate credo survey logistics along with local credo champion.
- Compliance with safety policies and procedures.
- Other responsibilities may be assigned and not all responsibilities listed may be assigned.
- Follow J&J Records Management Policies for Convenience Information, Records Retention Schedules,

Training and Education, Document Hold Notices, Records Cleanout, Inactive Records and Information Management, Vital Records, and third-party vendor if applicable.

**Qualifications**:
**EXPERIENCE AND EDUCATION**

8+ years’ experience in a project management position or equivalent.
- Engineering bachelor’s degree is preferred.
- Experience in the Medical Device industry or medical field.
- Demonstrated knowledge on medical manufacturing principles and practices, and procedures.
- Experience in medical industry project validation.
- Ability to work cooperatively with coworkers and the public.
- Ability to perform duties in accordance with policies and procedures and in to comply civil rights requirements.

REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and

AFFILIATIONS
- Must be fluent in English (speak, read & write).
- GMP/ ISO knowledge preferred.
- Ability to maintain good interpersonal relations at all levels of the organization.
- Capability Analysis.
- Ability in using the software related to the activities described spreadsheets, presentation, and word processing.
- High level of discernment and understanding of end-to-end supply chain processes to have foresight to key risk

areas and expertise to support risk mitigation.


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