Lavori attuali relativi a Senior Sterility Assurance Specialist - Sesto Fiorentino, Toscana - Lilly
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Senior Sterility Assurance Specialist
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Sesto Fiorentino, Toscana, Italia Lilly A tempo pienoLilly is a global healthcare leader headquartered in Indianapolis, Indiana. As a leading innovator in the pharmaceutical industry, we're dedicated to discovering and bringing life-changing medicines to those who need them.We're currently seeking a Drug Product Manufacturing Quality Assurance Specialist to join our team in ensuring the highest quality...
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Sesto Fiorentino, Italia Lilly A tempo pienoAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...
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Senior Sterility Assurance Specialist
2 mesi fa
We are seeking a highly skilled and experienced Senior Sterility Assurance Specialist to join our team at Lilly. As a key member of our Quality Assurance department, you will be responsible for ensuring the highest standards of sterility assurance in our parenteral manufacturing operations.
Key Responsibilities:- Provide technical leadership and guidance to our contract manufacturers on sterility assurance practices and procedures.
- Develop and implement sterility assurance risk management strategies to ensure the highest level of quality and safety in our products.
- Collaborate with our Quality Assurance team to ensure compliance with regulatory requirements and industry standards.
- Lead and participate in investigations and root cause analyses to identify and resolve sterility assurance-related issues.
- Develop and maintain technical documents, including SOPs, protocols, and reports, related to sterility assurance.
- Provide training and coaching to our team members on sterility assurance best practices and procedures.
- Bachelor's degree in Microbiology, Pharmacy, or Chemistry, with at least 8 years of experience in technical and quality functions within a parenteral manufacturing plant.
- PhD in Microbiology with at least 2 years of experience in technical and quality functions within a parenteral manufacturing plant.
- Strong technical knowledge of sterility assurance principles and practices.
- Excellent communication and leadership skills.
- Ability to work effectively in a cross-functional team environment.
- A competitive salary and benefits package.
- Opportunities for professional growth and development.
- A dynamic and collaborative work environment.
- The chance to work on challenging and meaningful projects that impact the lives of millions of people around the world.
We are an equal opportunities employer and welcome applications from diverse candidates. If you are a motivated and experienced professional looking for a new challenge, please submit your application today.