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 and 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:stylemargin:bottom:11.0px::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:stylemargin:bottom:11.0px::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 9001 and ISO 13485).: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:stylemargin:bottom:11.0px::Defined:term contract + lunch vouchers.:Working in an international environment.:Inspirational colleagues and 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.
