Worldwide Validation Engineer

Il y a 6 mois


Le PontdeClaix, France BD Temps plein

**Job Description Summary**: BD Medical - Pharmaceutical Systems is a global leader in supplying the pharmaceutical industry with innovative, high-quality, clinically-proven and customized pre-fillable parenteral drug delivery systems. Our offering includes an extensive portfolio of pre-fillable syringes, self-injection systems, safety and shielding solutions. Our products are designed to protect, package and deliver drug therapies and to maximize healthcare worker and patient safety.

**We are the makers of possible**:
BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

**Why Join Us?**

A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.

Become a maker of possible with us

Reporting into the Design Assurance organization, the Computer Systems Validation (**CSV) Validation Senior Engineer** is responsible for **developing low to medium complexity WW (worldwide) validation strategies** for the Business Unit.

**Main Responsibilities**:

- ** As a WW Validation leader, you drive validation process improvement leading cross-functional and multi-site extended validation teams (plant CSV/DI SME) without hierarchical authority. You represent the Business Unit on BD initiatives related to CSV/Data Integrity (DI) competencies & capabilities, processes, and tools.**:

- ** As a Validation expert, you are responsible for combining validation expertise (ex: computerized systems, automated manufacturing equipment, test methods ), problem-solving approaches and analytical skills to support projects/complex activities.**:

- ** In addition, this position plays an active role in the processes to ensure products meet customer/patient needs and quality standards consistently with both corporate and unit policies, while meeting all validation and other regulatory applicable requirements**:
**Profile**:

- ** Engineer/master’s degree in Quality management or Science**:

- ** 5-7** **years’ relevant experience like high volume and regulated industrial environment** in Healthcare / Pharmaceutical / Biologics / Medical Devices industry (computerized systems, automated manufacturing equipment, data integrity...)
- ** Perfect knowledge of the industrial approach of validation**
- ** Projects management skills**
- ** Knowledge of basic statistical tools**

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

**Primary Work Location**: FRA Le Pont-de-Claix Cedex

**Additional Locations**:
**Work Shift**:


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