Unfortunately, we are unable to offer visa sponsorship for this role.
This is a full time, permanent position, working a flexible 36.5 hour week, Monday – Friday.
You will provide analytical support to the client’s drug substance manufacturing and method development services, involving project analysis, method development, forced degradation studies and proof of concept method validation.
Job Responsibilities that you be covering:
- You will provide analytical support for Eurofins’ drug substance manufacturing and method development projects, delivering high-quality analytical testing in line with client and regulatory requirements.
- You will perform project analysis, method development activities, forced degradation studies, proof of concept validation work, and data interpretation to support scientific objectives.
- You will contribute to the authoring and review of key analytical documentation, including Analytical Testing Plans, method protocols, and validation protocols, according to your skills and experience.
- You will work independently and collaboratively within a multidisciplinary team, ensuring accurate, innovative, and timely delivery of analytical solutions.
- You will apply strong technical expertise and problem-solving skills to investigate challenges, think logically, and develop effective scientific approaches to complex projects.
- You will communicate scientific findings and ideas effectively with internal and external stakeholders while contributing to a culture of continuous improvement, knowledge sharing, and professional development within Eurofins.