...&D Director is part of the Management Team of Synres, and responsible for the Research and Development Department and Regulatory Affairs. The R&D Director reports to the Managing Director.Location : M...
...compliance with the quality system and manufacturer specifications. He/she delivers technical assistance at customer sites and provides documentation to internal and external customers. Who we are loo...
...Regulatory Affairs. Champion product quality, safety, and traceability in partnership with Quality and Supply Chain teams. Support production footprint decisions to ensure availability and cost‑effici...
...Management & Portfolio Strategy Direct the product management teams in shaping TAPI’s API portfolio strategy, including lifecycle management, differentiation, and competitive positioning. Partner with...
...Management & Portfolio Strategy Direct the product management teams in shaping TAPI’s API portfolio strategy, including lifecycle management, differentiation, and competitive positioning. Partner with...
...Compliance Program. Local monitoring of the risk matrix. Legal compliance: Ensure full compliance within key legal compliance areas, including duty of vigilance, competition, anti‑bribery and anti‑mon...
...compliance with the quality system and manufacturer specifications. He/she delivers technical assistance at customer sites and provides documentation to internal and external customers. Who we are loo...
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...
...Regulatory Affairs. Champion product quality, safety, and traceability in partnership with Quality and Supply Chain teams. Support production footprint decisions to ensure availability and cost‑effici...
...& Department As the Senior Manager Corporate & Business Development Due Diligence you will be part of the Corporate and Business Development & Licensing Team, part of Corporate Strategy & Planning, an...
...management activities.This individual will work together with other drug safety team members in overseeing processing of (S)AE reporting, management of the processes for all (S)AE data and responses t...
...& health providers to provide country level education and clinical support. Working with the EMEA CMA Clinical Training Manager, the post will facilitate legal compliance with HCP interactions and edu...
...regulatory affairs and quality assurance teams to ensure HVAC systems meet regulatory requirements Qualifications Supervisory experience in HVAC construction, preferably within pharmaceutical or proce...
...affairs, regulatory affairs, and sales and marketing teams, to ensure awareness and compliance with safety requirements. Participates in strategic initiatives to enhance the overall safety profile of ...
...regulatory reporting systems and maintain proper record-keepingYour Profile3–5 years’ experience in medical device regulatory, quality, or product-related roles, or a relevant degree in Regulatory Aff...