QA AND REGULATORY AFFAIRS jobs in UNITED KINGDOM, United Kingdom

. This position would primarily support Amgen’s marketed products globally, as a Principal Regulatory Affairs CMC lead. The Manager... Regulatory Affairs and Strategy (GRAAS) organization under the Amgen Research and Development Division. We all work together...

Regulatory Affairs Specialist - Medical Devices company-West Yorkshire - £negotiable, pension, 23 days holiday + BHs... (increasing with length of service) This is an excellent opportunity to grow your Regulatory Affairs career in a hugely...

The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position... Regulatory Affairs - with experience in medicinal products. You will grow and maintain major portfolio in particular for the...

senior QA personnel in hosting or supporting Regulatory Authority Inspections. Supervision Requires some instructions... clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development...

. The QAC team work closely with departments such as Operations, Technical, Engineering, R&D and Regulatory Affairs... our Witney Centre of Excellence, we have a fantastic opportunity for a Lead QA Engineer to join our expanding highly skilled team...

, distribution chain partners, Regulatory affairs team, ResMed Manufacturer team, operational, commercial and marketing teams...We are hiring a QA Engineer to join our Quality Assurance team in our Didcot office. Let's talk about the role: The...

QA Requirements: Oversee and manage all QA requirements for our CMOs, ensuring adherence to applicable GMP, GFSI..., and other quality regulations. Collaborate with subject matter experts from CD&D, Operations, and S&T to align QA processes...

resource requirements, risk, and/or complexity Work closely with Regulatory Affairs on deliverables for global regulatory... would be a plus if you also possess previous experience in: Supplier Auditing and/or Quality Assurance. IVD medical device regulatory affairs experience...

standards Additional Responsibilities Regulatory Affairs Manage the company medical device products on the Medical Device...​ QA Officer - UK M/F (28841) At Guerbet, we build lasting relationships so that to enable people to live...

-functional teams including QC, production, and regulatory affairs to resolve quality issues and drive continuous improvement...Quality Assurance Officer Are you ready to embark on a new QA journey in the heart of the pharmaceutical industry...

in conjunction with any third-party vendors to which regulatory affairs activities are outsourced in order to ensure... going forward enables regulatory affairs activities to be handled in an efficient and expeditious fashion. Team...

. Collaborate closely with cross-functional teams including QC, production, and regulatory affairs to resolve quality issues...​ ​ Quality Assurance Officer ​ Are you ready to embark on a new QA journey in the heart of the pharmaceutical...

: Internal: Global quality management, Site Quality Leads, R&D, Regulatory Affairs, Clinical Affairs, Quality Engineering... manufacturing and compliance with all applicable regulatory requirements. The scope is focused on Quality Compliance processes...

local and global submissions Partners with pharmacovigilance, regulatory affairs, in-country teams, and device QA... industry or in a clinical setting (preferred) Knowledge of global regulatory requirements for pharmaceutical, medical devices...

Partners with pharmacovigilance, regulatory affairs, in-country teams, and device QA for submissions and escalates requests... setting (preferred) Knowledge of global regulatory requirements for pharmaceutical, medical devices and combination products...

with our Regulatory Affairs and Quality Assurance (RAQA) team to provide support and coordination to functional areas of Global IT.../Microsoft project) Experience of working as part of a QA team within a regulated industry Good and clear communicator...

or pharmaceutical science) Demonstrable experience in formulation development or product development, regulatory affairs, ideally... of technical product stories Participation and arrangement of technical accredited audits Set formulation QA standards...