QUALITY SPECIALIST, IBERIA (TEMPORARY CONTRACT)

Location.
based in our offices in either Madrid or Lisbon, on a hybrid working schedule.
About the Role.
As a Quality Specialist for our Iberia country (Spain & Portugal), you will play a vital role in ensuring that our products meet the highest standards of quality and compliance.
You will be at the forefront of developing and maintaining quality-engineering methodologies, systems, and practices that align with both internal and external requirements.
This position serves as a pivotal link between our teams and regulatory standards, enhancing awareness and communication on quality initiatives.
In this role, you will be responsible for.
Implementing effective process and control systems to support product, qualification and distribution Leading the implementation of assurances, process controls, and CAPA systems to meet internal and external requirements.
Supporting quality disciplines, decisions, and practices as a key team member.
Utilizing systematic problem-solving methodologies to identify, prioritize, and resolve quality issues.
Developing and executing streamlined business systems to identify and resolve quality issues efficiently.
Advising management on potential improvements or enhancements to quality systems and processes.
Ensuring compliance with applicable standard operating procedures and regulatory standards.
What are we looking for in you.
3-5 years experience in a multinational company, preferably in the MedTech or Healthcare industry.
Excellent communication skills to effectively convey quality initiatives and requirements.
Fluent in English (C1 level); native level in either Spanish or Portuguese.
Strong teamwork and collaboration abilities to work across departments and functions.
Analytical mindset with a keen eye for detail in problem-solving.
Adaptability to evolving regulatory requirements and industry standards.
Leadership qualities to support team members, provide feedback, and guidance.
In-depth knowledge of quality-engineering methodologies and systems.
Familiarity with regulatory requirements such as FDA, MDD, PAL, CMDCAS, and ISO standards (especially ISO and ISO ).
Experience in implementing process controls, CAPA systems, and documentation control principles.
Ability to analyze and interpret complex information to ensure compliance and quality standards.
Proficiency in applying quality principles to various situations and work environments.
What we can offer to you.
Defined-term contract + lunch vouchers.
Working in an international environment.
Inspirational colleagues & culture.
Innovative environment.
Company with a purposeful mission.
Future development opportunities may exist.
Location.
based in our offices in either Madrid or Lisbon, on a hybrid working schedule.
We, Boston Scientific, are an equal employment opportunity employer.
We do not and will not make any personnel decisions (like recruiting, hiring, job assignments, and promotions) based on a person’s age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law.