Sr Quality Engineer and Veeva Vault Configuration

hace 6 meses

Tijuana, México Corza Medical A tiempo completo

**Vacancy Name**
- Sr Quality Engineer and Veeva Vault Configuration Specialist

**Location of Work**
- Tijuana, Mexico

**Employment Type**
- Full Time Employee

**Job Purpose Summary**
Responsible for the development, implementation and maintenance of Veeva System.
- Develop strategies and initiatives for maintaining the Documentation System aligned with medical devices standards and regulations requirements and the company goals and objectives.
- Primary responsibility is to maintain the daily activities within the Document Control function. This position has knowledge and experience of working in regulated environments (i.e. ISO 13485, 21 CFR Part 820, 21 CFR Part 11) and sufficient knowledge and experience using an electronic Quality system.
- **What you will do**
- Overall responsibility for supporting all activities related with Veeva System
- Training: Create and maintain training program by “Access Sub-Type” for New and Current Veeva Users
- Accesses: Supporting to obtain the New Accesses or changes in the “Access Sub-Type”
- Improvements: Participate in all projects related with Veeva updates
- Maintain: Veeva System
- Maintain Document Control Approval Matrix requirements.
- Stablishes systems and processes to ensure compliance of Document Control.
- Contributes to organizational change to create and sustain a work environment conducive to continuous improvement.
- Managed the Document Control team with task scheduling, work assignments, and other workload balancing activities.
- Mentor and train team members in Document Control processes
- Work on multiple projects simultaneously.
- Communicates effectively across teams to explain methodology, process, and results from analysis.
- Evaluate the accuracy and conformance to required procedures and performance improvement projects and initiatives.
- Support Audit efforts as requested.
- Other duties as assigned.

**What you will need**
**Education**:Bachelor's Degree in a science, technical discipline or Experience equivalent.
- **Experience**:At least 5- 10 years of QMS and leadership experience in medical devices.
- **Languages**:Bilingual -** **Strong verbal and written communications skills.
- **Other Knowledge, Skills, Abilities or **Certifications**:

- Demonstrated experience working with diverse cultures.
- Strong organizational skills. Strong verbal and written communications skills.
- Demonstrated capability/experience raising issues and concerns and constructively challenging leadership to drive appropriate change and compliance.
- Management skills
- Effective communication
- Trainer skills
- Ability to establish and maintain effective interpersonal relationships at various levels of the organization.
- Experience with GMP, GDP, QMS, Audits, etc. as part of a Quality Culture.

**What you will like**
We foster a work environment where all team members are empowered and encouraged to share their opinions and ideas. We encourage robust, fact-based debate. Our highly collaborative work environment results in the best decisions for Corza Medical and a shared mission to execute our plan together, on time and on budget.
- **Join our team.**
At Corza Medical, we are motivated by enabling our customers’ success. That starts with understanding their needs and developing products that enhance clinical outcomes. Our goal is to provide innovative, high-quality products and services that will ensure the continued success of our company and surgical professionals well into the future.

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