Company Description
Consider joining Eurofins where people are the most important element in our business. Eurofins Biopharma Product Testing is a leading contract lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide.
What can Eurofins offer you?
* At Eurofins we offer careers not just jobs.
* Developmental opportunities and career progression.
* Private Medical Insurance when with the company for 2 years for all roles.
* Income protection and life assurance.
* Free parking onsite.
* Additional annual leave days with continued service.
* The opportunity to work on life-saving products.
* Work-life balance.
* Sports and Social events.
Job Description
We currently have vacancies for Analysts within our expanding Gene Therapy team.
The purpose of this role is as follows:
* To perform routine and non-routine analysis, as requested by the laboratory.
* To prepare and approve results for tests in which they are deemed competent.
* To be aware of customers' requirements and strive to meet those requirements, keeping in mind the cycle is not complete until the customer has obtained their report.
* To deal with customer queries and telephone significant results to customers.
* To keep up to date with any technological or method revisions in their area, ensuring their training is complete and adjusting their work as required.
* To train other more junior members of staff in analytical techniques as required.
* To perform QC samples in accordance with company procedures.
* To revise SOPs as required by the laboratory.
* To participate in the company’s weekend rota and/or overtime schedule, as required.
* To be responsible for updating any relevant documentation when requested.
* To provide cover for other members of staff as required.
* To ensure that all documentation is completed on time, accurately, and legibly.
* To keep their training records up to date and to initiate training where possible.
* To identify any opportunities for improvement of quality and service and work with the team to implement continuous improvement.
Qualifications
* BSc in a scientific discipline or equivalent with at least 2 years relevant industrial experience in GMP lab.
* Experience required: qPCR, SDS-Page, ELISA, cell-based assays, and bioassays including replication competency testing.
* Specific experience in Analytical ultracentrifugation (AUC) is an advantage.
* Experience of working in a regulated cGMP environment is essential.
* Strong technical writing, presentation, and troubleshooting skills are essential.
* Ability to work independently within a team-based environment.
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