Project Manager Pharmaceutical Technical Regulatory Operations (m/f)

REFERENZNUMMER:

249914/11

IHRE AUFGABEN:

-Define project objectives, requirements, and assumptions necessary to develop project charter and project plans
-Plan, schedule, and control project activities to fulfill objectives and satisfy project requirements and strategy
-Develop and drive integrated project plans, aligning project tactics with project strategy
-Lead, coordinate, facilitate, and motivate all associated project resources to gain alignment on project goals and deliverables
-Lead risk management within project teams
-Manage projects within established scope, schedule, and budget
-Facilitate and lead effective project meetings and workshops,
-Manage change and conflict, and develop resource planning estimates to manage project workload and productivity
-In collaboration with project team and program manager, develop, execute and sustain effective project communication, training and change management plans

IHRE QUALIFIKATIONEN:

-Minimum BS/BA in life science, engineering, business or relevant experience
-Proven track record of effective project managements experience in biotechnology, medical/combination device and/or pharmaceutical operations groups
-Proficient knowledge and application of disciplined project management processes
-Familiarity with drug and/or medical device development process through FDA approval
-Working knowledge of regulatory requirements and processes
-Strong written, oral communication, facilitation and presentation skills
-Proficient in using MS Excel, Word, Project and PowerPoint
-Demonstrated ability for effective decision-making
-Proven ability to create strong working relationships
-Demonstrated ability to organize, lead, and execute on a variety of assignments and action plans;
-Ability to translate complex concepts into actionable, measurable tasks
-Fluent in English and German, French is a plus

WEITERE QUALIFIKATIONEN:

Project manager, Regulatory affairs manager