Senior Program Manager - Tijuana, México - Corza Medical

Corza Medical

Empresa verificada

Tijuana, México

hace 3 semanas

Publicado por:

Rodrigo Fernández

Reclutador de talento para beBee

Descripción

Vacancy Name

Senior Program Manager

Location of Work

Tijuana, Mexico

Employment Type

Full Time Employee

Our brand promise

We deliver a collaborative experience by working directly with the surgical community to ensure you get the exact surgical tools you need at the right time and the right price.

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Remarkable service
A seamless, personal process designed around you and your needs.
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Trusted performance
Our product family is the result of years of experience championing surgeons and listening to their expertise.
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Outstanding value
No matter the surgical specialty, we deliver quality products for all markets.

Our people promise
Excellence is our Specialty and what makes us successful is our people.

We are committed to fostering a positive, empowering and growth-oriented environment where all team members are encouraged to share their opinions and ideas.

That means you will work alongside an accomplished and highly collaborative team that inspires commitment to our goal in attaining excellence in everything they do.

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Job Purpose Summary

The Senior Program Manager - Quality Projects is responsible for the clear definition, scoping and time calculations of the quality programs established by Corza.

This position ensures resources are managed accordingly for the purpose of delivering quality projects within budget, withing their time constraints, and with the personnel necessary.

This position will interact with all levels in the organization and needs to be a strong Individual adept in leading indirectly, communicating assertively with executive members of the organization, and managing resources to reach established goals.

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What you will do

Develop and lead a centralized process for Quality projects.
Create detailed and accurate project schedules; implement project reporting tools to support management tracking, reporting and stagegate decision making.
Set goals and objectives for project deliverables and assist in the evaluation of the team against these metrics. Identify opportunities for improvement proactively.
Gains consensus for the optimal solution by effectively organizing and presenting information to stakeholders and Executive Leadership.
Ensure quality compliance activities are resourced and executed.
Maintain full regulatory compliance with EHS, FDA, ISO 13485, OSHA and other legal requirements.
Contribute to and/or lead process improvements to budget, risk, scheduling, change management and cost tracking tools, metric reporting, reporting procedures and operational effectiveness.
Analyze quality levels through use of Six Sigma or related tools and develop and implement improvement programs.
Identify and resolve issues that may jeopardize project schedules or improve project time. Keep management fully informed in a timely manner with regard to any and all potential problems on a project.
Drive crossfunctional accountability and project management.

What you will need

Bachelor's degree in related field, preferably Engineering
8 + years of experience in Medical Device with at least 4 years in Program Management/Project Management
Excellent verbal and written communication skills and interpersonal skills are required. Meeting organization and presentation skills required.
Must be bilingual in Spanish and English.
Effective at developing Gantt charts, managing time and prioritizing projects in order to meet established deadlines.
Effective collaboration and communication skills; ability to lead cross functionally without direct reporting lines.
Proficiency in project management tools including Microsoft Office Suite (Outlook, Word, Excel, PowerPoint, MS Project) is required.