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Sr. Specialist Supplier Quality - Quality Assurance - Basel
View: 147
Update day: 26-03-2024
Location: Basel Basel-Stadt BS
Category: Quality Assurance / Quality Control
Industry: Financial Services Biotechnology Pharmaceuticals
Position: Associate
Job type: Full-time
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Job content
The RoleModerna is seeking a highly motivated and dynamic Sr Specialist Supplier Quality, in Basel, Switzerland to complement our growing team and provide in the Supplier Quality and Customer Quality programs for Moderna’s commercial products to our international operations.
The Sr Specialist Supplier Quality will primarily work with Suppliers, Customers and internal stakeholders such as Commercial Operations, Technical Development, Regulatory Affairs, Quality Control and Manufacturing Science & Technology (MS&T) to support the Supplier Management program of Moderna.
The candidate will mainly manage Supplier Change notifications, conduct and manage supplier and customer Audits, negotiate and manage Quality Agreements and contribute to develop and maintain Moderna’s Quality governance program. Additionally, the individual will maintain the relevant processes and records in the Moderna eQMS with regards to the aspects above.
Here’s What You’ll Do
- Support the Supplier and Customer programs, systems, procedures and processes for Moderna’s international organization.
- Initiate and manage Supplier Change notifications.
- Initiate and Manage Quality Agreements
- Participate and Conduct Supplier and Customer Audits.
- Participate and chair the international Supplier Review Board.
- Monitor Supplier metrics to ensure an appropriate level of oversight is given.
- Support implementation and development of Quality processes with Moderna’s CMOs.
- Contribute to Quality Initiatives and projects as required.
- Bachelor’s degree, preferably in Sciences with applied Quality industry GXP experience of 5 to 8 years.
- Working knowledge of relevant EU and global regulations regarding Complaint management in the pharmaceutical industry
- Excellent interpersonal skills using a team-oriented approach to project management and problem solving for complex issue resolution in a scientifically sound and understandable way.
- Certified Lead auditor with significant audit experience will be an advantage
- Communicates excellently with internal/ external stakeholders in English (Additional languages a plus)
- A curious and bold mindset that allows you to constantly learn and challenge the status quo
- Dynamic personality who enjoys working in a fast-paced environment
In 10 years since its inception, Moderna has transformed from a science research-stage company advancing programs in the promising-but-still-unproven field of messenger RNA (mRNA), to an enterprise with its first medicine having treated millions of people, a diverse clinical portfolio of vaccines and therapeutics across six modalities, a broad intellectual property portfolio in areas including mRNA and lipid nanoparticle formulation, and an integrated manufacturing plant that allows for both clinical and commercial production at scale and at unprecedented speed. Moderna maintains alliances with a broad range of domestic and overseas government and commercial collaborators, which has allowed for the pursuit of both groundbreaking science and rapid scaling of manufacturing. Most recently, Moderna’s capabilities have come together to allow the authorized use of one of the earliest and most-effective vaccines against the COVID-19 pandemic.
Moderna’s mRNA platform builds on continuous advances in basic and applied mRNA science, delivery technology and manufacturing, and has allowed the development of therapeutics and vaccines for infectious diseases, immuno-oncology, rare diseases, cardiovascular diseases and auto-immune diseases. Today, 24 development programs are underway across these therapeutic areas, with 13 programs having entered the clinic. Moderna has been named a top biopharmaceutical employer by Science for the past six years. To learn more, visit
Moderna is a smoke-free, alcohol-free and drug-free work environment.
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Deadline: 10-05-2024
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