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A familyowned company bioMrieux has grown to become a world leader in the field of in vitro diagnostics. For almost 60 years and across the world we have imagined and developed innovative diagnostics solutions to improve public health. Today our teams are spread across 45 countries and serve 160 countries with the support of a large distribution network.
Come and join a familyowned global company with a longterm vision and a humancentered culture.
Fixed Term 12 Months Contract
Reporting to the UK Quality/Regulatory Manager this position is responsible for the management of regulatory tasks for the UK/Ireland cluster. This includes acting as a point of contact for regulatory matters and managing integration of UKCA requirements for In Vitro Diagnostics (IVD) to ensure compliance by the relevant deadlines. The position will also have the responsibility of managing the MHRA registration portfolio and conducting local regulatory surveillance activities.
This position will require presence in our office in Basingstoke (hybrid working policy)
What will your responsibilities be within bioMrieux
Who are you
bioMrieux welcomes applications from all individuals regardless of race national origin gender age physical characteristics social origin disability union membership religion family status pregnancy sexual orientation gender identity gender expression or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.
Required Experience:
Unclear Seniority
Contract