Quality Assurance Specialist

BD; Cañada; Presencial; EUR 55.000 - 59.000; Jornada completa

Descripción de la vacante

BD is seeking a Quality Compliance Specialist to coordinate the regional program across EMEA, leading internal audits and supporting external regulatory inspections. The role drives CAPA actions, management reviews, and QMS improvements to ensure compliance and quality excellence.

Requirements include a Life Sciences, Engineering, or Quality Management degree and 3–5 years in regulated industries, with English fluency and willingness to travel within EMEA. Valencia, ESP location.

Formación

• 3–5 years of experience in Quality Assurance, Quality Compliance, or Quality Systems in regulated industries.
• Experience planning and conducting internal audits and supporting external regulatory inspections.
• Strong knowledge of QMS and applicable standards (ISO 13485, FDA QSR, MDR).

Responsabilidades

• Coordinate and execute the regional Quality Compliance program across EMEA.
• Plan, conduct, document, and report internal audits across EMEA locations.
• Support external audits and regulatory inspections, including CAPA management.
• Prepare and consolidate Management Review inputs and quality metrics.
• Promote ongoing improvement of the Quality Management System and audit readiness.

Conocimientos

Quality Assurance

Audit Experience

Regulatory Compliance

Quality Metrics

Cross-functional Collaboration

Educación

Bachelor's degree in Life Sciences, Engineering, Quality Management

Descripción del empleo

We are the people who give possibilities purpose

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.

Job Description

The Quality Compliance Specialist is responsible for coordinating and executing the regional Quality Compliance program across EMEA. This role leads the planning and performance of internal audits, supports external regulatory and certification audits, prepares Management Review reports, and contributes to the effective operation and continuous improvement of the Quality Management System (QMS) throughout the region.

Key Responsibilities

• Develop and maintain the annual EMEA internal audit program based on risk, regulatory requirements, and business priorities.
• Plan, conduct, document, and report internal audits across EMEA locations and functions.
• Monitor audit findings and support site management in the timely implementation and closure of corrective and preventive actions (CAPAs).
• Coordinate and support external audits, including notified body, certification body, customer, and regulatory inspections.
• Prepare and consolidate Management Review inputs and reports, ensuring accuracy, completeness, and timely delivery.
• Analyze quality metrics and trends to support Management Review discussions and decision‑making.
• Support maintenance and continuous improvement of the Quality Management System in accordance with applicable regulations and standards.
• Provide guidance to functions and sites on quality compliance requirements, audit readiness, and best practices.
• Support Quality activities across the region, including CAPA management, quality risk management, document control, change management, training compliance, and quality reporting, as required.
• Collaborate with regional and global Quality teams to ensure alignment of compliance initiatives and quality objectives.
• Promote a culture of quality, compliance, and continuous improvement throughout the organization.

About you

• Bachelor's degree in Life Sciences, Engineering, Quality Management, or a related discipline.
• Minimum 3–5 years of experience in Quality Assurance, Quality Compliance, or Quality Systems within a regulated industry (Medical Devices, Pharmaceutical, Biotechnology, or similar).
• Experience planning and conducting internal audits. Experience supporting external audits and regulatory inspections. Experience preparing management review materials and quality metrics analysis.
• Strong knowledge of Quality Management Systems and applicable regulations and standards (e.g., ISO 13485, FDA QSR, MDR, or equivalent). Certified Internal Auditor qualification is preferred.
• Fluent in English; additional European languages are an advantage.

Ability to travel within the EMEA region as required.

Salary range for this role 55000€ - 59000€

Why Join Us?

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 healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face‑to‑face collaboration supports your learning, your progress, and your success.

To learn more about BD visit https://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to 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, and other legally protected characteristics.

Primary Work Location

ESP Valencia - Paterna

Salary Range Information

€37,700.00 - €60,350.00 EUR Annual