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Posted 3 days ago by Arevna
Overall Purpose Undertake key technical and regulatory activities to support the continued FDA/CE/UKCA marking of company devices. Performs complaint investigations and conducts active maintenance of technical documentation across the full product lifecycle. 2. Key Tasks. Undertake customer … more
Posted 5 days ago by SciPro
We are supporting them on their search for a Senior Regulatory Affairs Associate within Pharmacovigilance. The successful candidate will join their Product Development Department and will be responsible for managing the day-to-day pharmacovigilance activities and lead on the … more
