Joint Skills in Quality Assurance and IT Required
We are seeking a skilled QA IT MES Specialist to join our team.
* As a Global Leader in Biopharmaceutical Innovation, we value excellence and compliance in our electronic batch record system implementation.
* This is an ASAP opportunity with an initial contract of 6 months; however, extension until the end of 2025 is highly probable.
Key Responsibilities:
* You will represent quality in site and global project teams, providing oversight and expertise on Computerized System Validation (CSV) and validation activities.
* You will ensure all quality aspects of the project comply with Global Policies, SOPs, and GMP regulations.
* You will review and approve key documentation, including risk assessments, validation protocols, and configuration specifications.
* You will collaborate with project teams to address quality issues, organize QA activities, and promote compliance with data integrity standards.
* You will act as a key QA liaison, ensuring seamless communication among stakeholders and supporting an agile validation approach.
Your Qualifications:
* You should have proven experience in Computerized System Validation (CSV) and a strong understanding of cGxPs and industry standards.
* Fluency in English and French is essential.
* You should possess exceptional communication and organizational skills to collaborate across diverse teams.
* You should have a proactive mindset with flexibility and dedication to meet project timelines.
* Residency or work permit in Switzerland is mandatory; cross-border workers are welcome.
What You'll Gain:
* You will be part of a globally renowned biopharmaceutical company.
* You will collaborate on cutting-edge projects that shape the future of healthcare.
* You will work in a state-of-the-art facility overlooking the beautiful Lake of Neuchâtel.