etc.). Key Responsibilities: Ensure that all activities and interactions are conducted with due regard of the company (e.g. post marketing clinical activities such as registry/database projects, epidemiological studies (phase IV), IIS projects, etc.): all activities to comply with applicable local laws, guidelines (GPRD) SOPs. Ownership of pre-launch medical activities (BD, new products assessments, market research potential research collaborations, or lecture/meeting support (Round Tables, Congresses, Symposia, etc.); and
launch activities Plan, coordinate and drive product reformulation and product improvement activities Plan drive test method development and validation activities Lead and coordinate all technology transfer projects plan He/she must be able to manage change and take active leadership in timely decision-making Responsibilities: Drive and co-ordinate test method validation activities at the EMO Compile and ensure execution of process responsibilities Analyze risk and instigate avoidance activities: establish contingency plans and identify trigger
launch activities Plan, coordinate and drive product reformulation and product improvement activities Plan drive test method development and validation activities Lead and coordinate all technology transfer projects plan He/she must be able to manage change and take active leadership in timely decision-making Responsibilities: Drive and co-ordinate test method validation activities at the EMO Compile and ensure execution of process responsibilities Analyze risk and instigate avoidance activities: establish contingency plans and identify trigger
for a Senior Regulatory Pharmacist. Job Purpose: Support the Regulatory team to provide superior Regulatory regulatory compliance is maintained or enhanced. Support activities such as internal audits or regulatory agency operations analysis Basic cost management skills Active learning Strategic thinking Ability to cope with