Quality Engineer

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/79q9dm

ppAs a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow- because at LivaNova, we don't just treat conditions - we aspire to alter the course of lives. /ph3Who are we looking for: /h3pAre you passionate about quality, product development, and ensuring that healthcare products meet the highest standards of safety and compliance? We are looking for a Quality Engineer to join our Quality team and play a key role in supporting product development, process validation, and quality improvement activities within a highly regulated medical device environment. In this role, you will work closely with RD, Manufacturing, and Quality teams, contributing to the development and maintenance of innovative medical devices while ensuring compliance with international quality and regulatory standards. This opportunity is ideal for someone with experience in Product Development, Design Control, and Quality Assurance, who enjoys solving complex quality challenges and collaborating across functions to drive continuous improvement. /ph3Your new role: /h3ulliPartner with RD and Engineering teams to define product and process requirements. /liliSupport Design Control activities throughout the product development lifecycle. /liliReview product verification and validation plans, protocols, and reports. /liliReview process validation activities to ensure compliance with quality requirements. /liliParticipate in change impact assessments and evaluate quality implications of product or process changes. /liliCoordinate investigations related to verification and validation failures. /liliEstablish and maintain product quality control plans. /liliIdentify and lead quality improvement initiatives within manufacturing operations.



/liliAnalyze nonconforming products and support disposition decisions. /liliLead root cause investigations for product and component failures identified during production or through customer complaints. /liliManage CAPA activities and analyze quality trends to identify improvement opportunities. /liliSupport suppliers and external manufacturing partners in addressing quality issues and nonconformities. /liliContribute to risk assessments and product safety evaluations, including Health Hazard Assessments (HHA) when required. /li /ulh3How you'll make an impact: /h3ulliEnsure that medical devices are developed and manufactured in compliance with regulatory and quality requirements. /liliAct as the Quality representative within cross-functional product development projects. /liliSupport the successful launch and maintenance of products by identifying risks and quality concerns early in the process. /liliImprove manufacturing quality performance through structured problem solving and continuous improvement initiatives. /liliDrive investigations and corrective actions that enhance product reliability and patient safety. /liliContribute to maintaining a strong Quality Culture across the organization. /li /ulh3About you: /h3ulliDegree in Engineering, Chemistry, Biology, Physics, or another scientific discipline. /lili1-3 years of experience within Quality Assurance in the Medical Device or Pharmaceutical industry. /liliExperience supporting product design and development activities. /liliGood understanding of Product Development Processes and Design Control principles. /liliKnowledge of ISO 13485 and Quality Management Systems. /liliUnderstanding of Good Manufacturing Practices (GMP). /liliExperience with validation activities, CAPA management, nonconformance investigations,



and root cause analysis is considered a strong advantage. /liliStrong analytical and problem-solving skills. /liliAbility to work effectively in cross-functional teams. /liliGood communication and stakeholder management skills. /liliFluent English, both written and spoken. /liliProficient in Microsoft Office Suite. /li /ulh3What you will find: /h3ulliThe opportunity to work on products that directly impact patients' lives. /liliExposure to the full product development lifecycle within the medical device industry. /liliA collaborative environment where Quality, RD, and Manufacturing work closely together. /liliThe chance to develop expertise in Design Quality, Validation, Risk Management, CAPA, and Product Development Processes. /liliContinuous learning opportunities within a highly regulated and innovation-driven industry. /liliA dynamic and international environment focused on quality, compliance, and continuous improvement. /liliCareer growth opportunities within Quality Engineering and Product Development functions. /li /ulpLocation: Mirandola, Italy /ph3WHAT WE CAN OFFER YOU: /h3ulliNational Collective Bargaining Agreement: CCNL Gomma Plastica /liliLevel: A/C /liliBase Salary range: € 31.000 – € 50.000 /liliBonus: 0-5% /liliActual compensation will be determined based on relevant experience, qualifications, and internal equity considerations. /li /ulpWe offer a competitive benefits package including: /pulliFlexible working options. /liliMedical insurance. /liliPension scheme. /liliEmployee stock purchase plan. /liliGlobal recognition programme. /liliAdditional benefits (e.g. meal vouchers, flexible benefits, local bonuses) may apply depending on location. /li /ulpWelcome to impact. Welcome to innovation. Welcome to your new life. /ppWe treat our work as if lives depend on it - because they do. /ppAs a people-oriented company, our employees around the world are fully committed to making the world a better place. /ppOur team's commitment to improve quality of life is the embodiment of our company Vision and Mission, making a difference every day for patients and their families. /p /p #J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/79q9dm