Staff Quality Systems Auditor

hace 1 semana

Ciudad Juarez, México Johnson & Johnson SA de CV A tiempo completo

**STAFF QUALITY SYSTEMS AUDITOR**
**-**
**2306135150W**

**Descripción**

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.**

**JOB SUMMARY**
Conducts audits— planned and unplanned — to verify compliance with government regulations and applicable standards, in addition to company policies and procedures. Give guidance or advice to the organization as it relates to compliance, when required.
- **DUTIES & RESPONSIBILITIES**
Under general direction and in accordance with all federal, state, and local laws/regulations and procedures and guidelines of the Johnson & Johnson Corporation, this position:
- It ensures that Quality System Audits comply with the requirements of QSR/GMP and ISO Standards
- Conducts internal audits of the Quality System for the purpose of verifying compliance with government regulations and applicable standards, in addition to company policies and procedures.

Conducts good laboratory practice (GLP) audits as required.
- Gives guidance or advice as it relates to compliance with applicable standards and regulations.
- Performs re-audits to deficient aspects and to implement corrective and preventive actions as necessary and required.
- Assigns classifications to internal audit observations and documents audit results in written reports that can be distributed and reviewed by appropriate management.
- Monitors the effectiveness of corrective actions documented in observation responses.
- You can be the lead auditor of a team of auditors, technical experts, auditors-in-training, and/or volunteer auditors.
- Reviews ownership of responses to audit observations, also acts as an advisor to other areas that are not being audited by him/her, giving advice on audit observation responses.
- Maintains audit report files, re-audit files and responses to audits carried out.
- Accompanies external auditors, representatives of government agencies or those required by management during the execution of an applicable audit.
- Conducts audits at other J&J sites when required by management.
- Complies with and reviews compliance metrics and communicates them to site management and the Franchise. Prepares information for Management review boards.
- Participates in the formulation of Regulatory Policies and Procedures in compliance with applicable local, state and federal standards and regulations through the development of Franchise Documents.
- It is kept up to date on government regulations and applicable standard changes through publications, participation in seminars or by collaboration with organizations.
- Is responsible for communicating business-related matters or opportunities to the next managerial level
- For those who supervise or manage personnel, they are responsible for ensuring that subordinates follow all of the Company's guidelines related to Health, Safety and Environment practices and that all necessary resources to do so are available and in good condition, if applicable.
- Is responsible for ensuring personal and Company compliance with all Federal, State and Local company regulations, policies and procedures
- Performs other assigned tasks as needed.

**Calificaciones**

**EXPERIENCE AND EDUCATION**
- Bachelor's degree in Engineering or related areas (desirable).
- It usually requires 5 years of experience and/or training in related areas.
- Master's degree of preference.
- Experience working in an FDA-regulated environment (desirable)

**REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS**
- Effective communication skills - oral and written - (English and Spanish).
- Analytical skills to interpret scientific and technical publications and legal documents.
- Ability to select, manage and lead a team during an audit.
- Ability to respond to questions or complaints from clients, regulatory agencies or members of the business community.
- Skills to present

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