QRA Specialist Iberia - Temporary 1 year.

BD; San Agustín del Guadalix; On-site; EUR 33,000 - 52,000; Full time

Job summary

BD is seeking a QRA Specialist Iberia to support regulatory compliance, quality excellence, and market access for Spain and Portugal within the Iberia QRA team. The role involves reviewing materials, maintaining QMS, and collaborating with local, regional, and global teams.

Requires aBachelor’s degree in Life Sciences/Engineering/Pharmacy/Quality/Regulatory Affairs and 1–3 years in QA/RA. Fluent English is essential; Spain-based location is ESP San Agustin del Guadalix.

Qualifications

• Bachelor’s degree in Life Sciences, Engineering, Pharmacy, Quality, Regulatory Affairs or related field.
• 1–3 years in Quality and/or Regulatory Affairs within a regulated industry.
• Strong knowledge of MDR, IVDR, ISO 9001:2015 and ISO 13485:2016 and local regulations.
• Fluent English, written and spoken.

Responsibilities

• Support regulatory compliance for the assigned portfolio and country (Spain and Portugal) including product notifications.
• Provide regulatory support to business initiatives and market access projects.
• Review promotional materials and labelling for regulatory compliance.
• Provide QRS support to cross-functional projects with local/regional/global QRA teams.
• Support maintenance and improvement of Quality Management System activities.
• Contribute to certification maintenance and audits, inspections and management reviews.
• Support CAPA activities and resolution of quality issues.
• Assist the QRA team and broader organization on additional activities as needed.

Skills

Regulatory Affairs

Quality Management

MDR/IVDR knowledge

ISO 9001/13485

Regulatory documentation

Stakeholder communication

Analytical skills

Education

Bachelor’s degree in Life Sciences/Engineering/Pharmacy/Quality/Regulatory Affairs

Job description

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 QRA Specialist Iberia serves as part of the local QRA team to conduct the activities at Iberia level for Go to Market activities, conducting the support to local stakeholders and regional QRA teams to ensure regulatory compliance, quality excellence, and uninterrupted market access while aligning local execution with EMEA QRA priorities.

The position requested will be working within the Iberia QRA team

Main responsabilities will include:

• Support regulatory compliance for the assigned portfolio and country scope (Spain plus Portugal) for the assigned portfolio and country scope, including preparation, submission, tracking and maintenance of product notifications.
• Provides regulatory support to business initiatives, market access projects, tenders, as applicable.
• Reviews promotional materials and labelling, as assigned, ensuring compliance with applicable regulatory and internal requirements.
• Provides QRS support to business activities and cross-functional projects, while collaborating closely with local, regional, and global QRA teams.
• Support maintenance and continuous improvement of assigned Quality Management System activities, ensuring compliance with internal procedures and applicable external requirements.
• Contribution to certification maintenance and audit readiness, supporting inspections, training activities, management reviews, and follow-up actions.
• Support CAPA activities, and resolution of quality issues within the assigned scope.
• Supports the QRA team and broader organization on additional activities as required, adapting to evolving business and priorities while contributing to overall QRA and business success.

Education and Experience:

• Bachelor´s degree in Life Sciences, Engineering, Pharmacy, Quality, Regulatory Affairs, or a related field, or equivalent experience.
• 1 - 3 years experience in Quality and/or Regulatory Affairs within a regulated industry.

Knowledge and Skills:

• Strong knowledge of European Medical devices Regulation (MDR), IVDR, ISO 9001:2015, ISO 13485:2016 and local regulations.
• Ability to interpret regulatory requirements, assess impact, and communicate effectively to stakeholders.
• Strong organizational, analytical, and collaboration skills, with the ability to adapt in evolving regulatory and business contexts.
• Fluent English language skills. both written and verbal, with the ability to effectively communicate and collaborate in an internal business environment.

Salary range for this role: EUR 36.000

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.

Required Skills

Optional Skills

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Primary Work Location

ESP San Agustin del Guadalix

Additional Locations

Work Shift

At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You."

Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.

Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.

Salary Range Information

€32,700.00 - €52,350.00 EUR Annual