stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that Pharmacy Council -5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable experience
experience of working in several groups in regulatory affairs or experience at a health authority Knowledge of management of a skill group such as CMC, Regulatory affairs project management, etc. Responsible for skill across the global, regional and local Regulatory Affairs interface enabling rapid and effective submissions
management of a skill group such as CMC, Regulatory affairs project management, etc. Responsible for skill across the global, regional and local Regulatory Affairs interface enabling rapid and effective submissions experience of working in several groups in regulatory affairs or experience at a health authority Knowledge of
Pharmaceutical Industry requires a Regulatory Affairs Manager in Aeroton. Lead the Regulatory team to stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that Council Minimum of 5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrated experience
the Pharmacutical Industry requires a Regulatory Affairs Pharmacist in Aeroton. Support the Regulatory team Pharmacy Council 2-5 years' experience in Regulatory Affairs, preferably in orthodox, human medicines Demonstratable
The enforcement of the Council's Collective Agreement. Managing the activities of the Chamber's Inspectorate and Inspectorate staff. Managing and Administering the Chamber's dispute resolution function, as determined by the LRA and the Council's Constitution. Managing the administrative function of
A long-established leader in the pharmaceutical sector has an opportunity for an RA Manager to lead their team of RA pharmacists and RA scientists - about 4 to 8 people in the team. The position requires no dossier compilation from you - you will strategically manage the team and ensure output. You
dossier registrations in eCTD format, updates, pre and post-reg. amendments etc. B.Pharm degree 2 - 4 years
Reference: CT004363-SM-1 JOB SUMMARY Responsible to ensure that regulatory submissions and compliance are executed for all products. Develop and communicate with head office on the regulatory strategy and life cycle management of all products. Represent our company with the local authority and other
made from human plasma is seeking a Regulatory Affairs Pharmacist who will be responsible to put current to clinical trials, pharmacovigilance and other post-marketing requirements Serve as back up to other regulatory resources in a timely manner Regulatory affairs administration Update the paper and electronic