Bioanalytical Scientist &; Potency Assays
Are you experience in the laboratory and would like to work in a leader in the biopharmaceutical industry?
About the Client
Our client is an international leader in the Swiss life sciences sector, based in Basel, a global hub for pharmaceutical innovation. Known for delivering cutting-edge solutions in biotechnology and biomanufacturing, the company fosters a collaborative and technically advanced workplace environment.
Job Description
We are currently seeking a skilled Laboratory Scientist that will be supporting analytical potency testing and method optimization. This role focuses on assay execution, documentation, and quality-driven lab practices within a fast-paced bio-analytics environment. The ideal candidate will carry out various binding and functional assays to support development and testing activities. You'll also contribute to improving lab operations and assist with troubleshooting.
Responsibilities
* Conduct binding and functional assays such as ELISA, SPR, CBA, or enzyme-based methods.
* Perform method development, optimization, and pre-validation of analytical techniques.
* Carry out buffer preparation and routine lab maintenance tasks.
* Document all testing activities in accordance with Good Documentation Practices (GDP).
* Participate in non-GMP batch release, formulation, and stability testing of drug products.
* Support equipment calibration and standard laboratory procedures.
* Assist in drafting method SOPs, validation protocols, and technical reports.
* Investigate and troubleshoot analytical method or instrumentation issues.
Requirements
* Degree or apprenticeship in Biology, Biochemistry, Chemistry, or a related scientific discipline.
* Minimum 5 years of industry experience in a laboratory within the pharma or biotech sector.
* Available to start in May.
* Proven ability to conduct, analyze, and document scientific assays and experiments.
* Familiarity with analytical software such as LIMS, Electronic Lab Notebooks, or SoftMax Pro.
* Strong written and verbal communication skills in English.
* Capable of working independently while contributing to a team environment.
* Understanding of GDP and ISO documentation standards.
* 1 year contract through Oxford Global Resources.
* Work at a pharmaceutical leader in a state of the art facility.
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