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
experience of working in several groups in regulatory affairs or experience at a health authority
Knowledge
management of a skill group such as CMC, Regulatory affairs project management, etc.
Responsible for
across the global, regional and local Regulatory Affairs interface enabling rapid and effective submissions
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
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
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
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
with APM/DP and inbound departments on stock availability and requirements. Work closely with outbound feedback to Account Planner and KAM on stock availability (qty/ETA) and possible stock outs or delays the working week Minimum of three night away from home per month Monthly
Solution selling in various business sectors Industrial Software. Solution selling in various business sectors of OT, Industrial software, industrial automation, instrumentation and control. Client Meetings and engagement Customer Relationship Management, lead and Opportunity management Building and