Junior GPRM / Regcmc Manager (NOVJP00026608) (m/f)

REFERENZNUMMER:

378079/29

IHRE AUFGABEN:

-Formulate and lead global CMC regulatory strategy for development projects or marketed products with a focus on creativity and innovation, maximizing the business benefit balanced with regulatory compliance
-Proactively communicate CMC regulatory strategy, key issues and any other critical topics throughout the life cycle in an adequate and timely manner to interdisciplinary project teams and to appropriate management level in regulatory, technical development, and technical operations departments as appropriate
-Lead and implement all global CMC submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects/products, while applying the global strategy into submissions
-Make quality regulatory decisions, balancing risks and benefits
-As early as possible, identify the required documentation and any content, quality and/or timeliness issues for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines
-Author high-quality CMC documentation for HA submission, applying CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements
-Establish and maintain a single point of contact with FDA or country affiliates, RA regional and TA groups for all communication on development and marketed products
-Establish and maintain sound working relationships with partners and customers
-Initiate and lead Health Authority interactions and negotiations as appropriate; setting objectives, preparing briefing books, coordinating and planning rehearsals and risk mitigation plans
-Lead and drive cross-functional CMC Health Authority Response Teams (HARTs) for as-signed development projects and/or marketed products, and prepare CMC responses, as appropriate
-Prepare and communicate CMC risk management assessments (RMA), contingency plans, and Lessons Learned exercises on major submissions with subteams and escalate with management as appropriate

IHRE QUALIFIKATIONEN:

-Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent
-Fluent in English required (oral and written), good skills in German desired (oral)
-Solid experience in regulatory and/or experience in drug/biopharmaceuticals
-Working knowledge of chemistry/biotechnology, analytics or pharmaceutical technology
-Knowledge of the drug development process desirable
-Ability to critically evaluate data from a broad range of scientific disciplines
-Demonstrated track record to successfully work in interdisciplinary teams, planning, coordinating, leading activities simultaneously on multiple projects
-Knowledge/experience of regulations, guidelines for NCEs and product life cycle maintenance desirable
-Ability to work successfully with extended, multinational project teams and coordinate activities simultaneously on multiple projects under pressure of time and workload

WEITERE QUALIFIKATIONEN:

Regulatory affairs assistant