Specialist, Supplier
pSelect how often (in days) to receive an alert: /p h3Specialist, Supplier ESO Quality Operations
- 1y Temporary Maternity Cover /h3 pAlfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South America, Asia, and Africa. /p pOver three years ago, we embarked on a transformative journey to become ba truly global innovative healthcare company with a leading focus on Gastrointestinal (GI) health /b. We have experienced remarkable growth, nearly doubled our revenues, expanding geographically, and integrating several key acquisitions. We have also evolved our portfolio, expanded into rare and specialty segments, and strengthened our pipeline and people's capabilities. /p pbBut our journey is far from complete /b In fact, this is just the beginning of a bold new chapter in Alfasigma's history. We are committed to advancing innovation and leveraging our deep expertise to provide better health and a better quality of life for patients and consumers worldwide and expand our reach across diverse markets. /p h3Scope of the Role /h3 pThe bSpecialist, Supplier ESO Operations /b supports quality oversight and compliance activities across the product lifecycle. The role is responsible for managing quality events, investigations, risk assessments, and change controls to ensure compliance with company requirements. The position also supports quality performance monitoring, issue resolution, and lifecycle management activities. /p h3Your Role /h3 pAs Specialist, Supplier ESO Operations, you will: /p ul liSupport the quality oversight of assigned suppliers to ensure compliance with applicable regulations, quality standards,
and company requirements throughout the product lifecycle. /li liManage supplier oversight, quality events, and risk management activities, including complaints, deviations, investigations, CAPAs, risk assessments, and OOS/OOT results, ensuring timely resolution of quality issues and effective mitigation of quality risks. /li liCoordinate change control activities impacting suppliers, manufacturing processes, materials, and externally manufactured products, ensuring compliant implementation and effective cross-functional alignment. /li liSupport product disposition and release decisions by ensuring that quality issues, investigations, deviations, and changes are appropriately assessed, documented, and resolved in accordance with applicable requirements. /li liMaintain supplier qualification, audit readiness, and ongoing compliance through supplier oversight activities, participation in audit programs, management of corrective action plans, and Quality Agreements. /li liSupport continuous improvement and technical quality initiatives by identifying process enhancement opportunities, supporting technology transfers and remediation projects, and collaborating with internal and external stakeholders to strengthen quality performance and compliance. /li /ul h3Who You Are /h3 h3Work Experience /h3 ul li3+ years of experience in supplier quality management within pharmaceuticals, food supplements, or medical devices.
/li /ul h3Education Training /h3 ul liBachelor's degree in Pharmacy, Chemistry, Life Sciences, or Engineering. /li liStrong knowledge of GMP, GDP, ISO 9001, ISO 13485, and applicable regulations for pharmaceuticals, medical devices, and food supplements. /li liSolid experience in supplier qualification, supplier oversight, audits, risk management, and quality systems within a regulated environment. /li liExperience with digital quality systems (eQMS, SAP, TrackWise, Veeva, or similar) and process improvement initiatives. /li liGood analytical skills, including KPI monitoring, performance reporting, and data analysis. /li liStrong communication and collaboration skills, with the ability to work effectively with internal teams and external partners. /li liExperience supporting quality improvement projects, technology transfers, and the resolution of complex quality issues. /li liFluent in English, both written and spoken; additional languages are considered an advantage. /li /ul bThe pay range is around €40,000 /b pThe compensation range indicated in this job posting represents an estimated average range for the position. The final remuneration will be determined based on the selected candidate’s experience, skills, and qualifications, in accordance with applicable EU pay transparency and pay equity requirements /p h3Why Join Alfasigma: /h3 pbAt Alfasigma, we foster a culture where the courage to innovate is key to our success. /bbr/We offer a competitive salary, comprehensive benefits, and extensive opportunities for professional growth and development. /p pOur commitment to people and patients is at the heart of everything we do. We value diversity and welcome individuals with unique perspectives and experiences. We believe that o
- 1y Temporary Maternity Cover /h3 pAlfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South America, Asia, and Africa. /p pOver three years ago, we embarked on a transformative journey to become ba truly global innovative healthcare company with a leading focus on Gastrointestinal (GI) health /b. We have experienced remarkable growth, nearly doubled our revenues, expanding geographically, and integrating several key acquisitions. We have also evolved our portfolio, expanded into rare and specialty segments, and strengthened our pipeline and people's capabilities. /p pbBut our journey is far from complete /b In fact, this is just the beginning of a bold new chapter in Alfasigma's history. We are committed to advancing innovation and leveraging our deep expertise to provide better health and a better quality of life for patients and consumers worldwide and expand our reach across diverse markets. /p h3Scope of the Role /h3 pThe bSpecialist, Supplier ESO Operations /b supports quality oversight and compliance activities across the product lifecycle. The role is responsible for managing quality events, investigations, risk assessments, and change controls to ensure compliance with company requirements. The position also supports quality performance monitoring, issue resolution, and lifecycle management activities. /p h3Your Role /h3 pAs Specialist, Supplier ESO Operations, you will: /p ul liSupport the quality oversight of assigned suppliers to ensure compliance with applicable regulations, quality standards,
and company requirements throughout the product lifecycle. /li liManage supplier oversight, quality events, and risk management activities, including complaints, deviations, investigations, CAPAs, risk assessments, and OOS/OOT results, ensuring timely resolution of quality issues and effective mitigation of quality risks. /li liCoordinate change control activities impacting suppliers, manufacturing processes, materials, and externally manufactured products, ensuring compliant implementation and effective cross-functional alignment. /li liSupport product disposition and release decisions by ensuring that quality issues, investigations, deviations, and changes are appropriately assessed, documented, and resolved in accordance with applicable requirements. /li liMaintain supplier qualification, audit readiness, and ongoing compliance through supplier oversight activities, participation in audit programs, management of corrective action plans, and Quality Agreements. /li liSupport continuous improvement and technical quality initiatives by identifying process enhancement opportunities, supporting technology transfers and remediation projects, and collaborating with internal and external stakeholders to strengthen quality performance and compliance. /li /ul h3Who You Are /h3 h3Work Experience /h3 ul li3+ years of experience in supplier quality management within pharmaceuticals, food supplements, or medical devices.
/li /ul h3Education Training /h3 ul liBachelor's degree in Pharmacy, Chemistry, Life Sciences, or Engineering. /li liStrong knowledge of GMP, GDP, ISO 9001, ISO 13485, and applicable regulations for pharmaceuticals, medical devices, and food supplements. /li liSolid experience in supplier qualification, supplier oversight, audits, risk management, and quality systems within a regulated environment. /li liExperience with digital quality systems (eQMS, SAP, TrackWise, Veeva, or similar) and process improvement initiatives. /li liGood analytical skills, including KPI monitoring, performance reporting, and data analysis. /li liStrong communication and collaboration skills, with the ability to work effectively with internal teams and external partners. /li liExperience supporting quality improvement projects, technology transfers, and the resolution of complex quality issues. /li liFluent in English, both written and spoken; additional languages are considered an advantage. /li /ul bThe pay range is around €40,000 /b pThe compensation range indicated in this job posting represents an estimated average range for the position. The final remuneration will be determined based on the selected candidate’s experience, skills, and qualifications, in accordance with applicable EU pay transparency and pay equity requirements /p h3Why Join Alfasigma: /h3 pbAt Alfasigma, we foster a culture where the courage to innovate is key to our success. /bbr/We offer a competitive salary, comprehensive benefits, and extensive opportunities for professional growth and development. /p pOur commitment to people and patients is at the heart of everything we do. We value diversity and welcome individuals with unique perspectives and experiences. We believe that o