For our client in Basel we are looking for a Regulatory Affairs CMC Associate Manager for a 8-month contract.
Duration: asap to 20/12/2019
Job Purpose: Under supervision, provide timely preparation of high quality CMC regulatory documentation and support to contribute to global regulatory submissions and strategies.
Major Activities: * Author high-quality CMC documentation for HA submission, with support and guidance, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements throughout project lifecycle. * Prepare CMC responses to health authority questions during development, registration and product lifecycle. * Identify the required documentation for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines. * Identify content, quality and/or timeliness issues with source documents, or any other potential authoring issues that may impact submission quality or timelines, as early as possible. * Keep knowledge up to date with regard to regulatory guidelines and requirements in all global regions as well as for new technical trends. * Actively participate as a member of the global team by contributing to the regulatory strategy, identifying the critical issues and lessons learned. * Establish and maintain sound working relationships with partners and customers. * Assume activities in support of the general department such as DRAGON support, annual and product renewal writing, coordination/collection/storage of source documentation needed for direct submission to HAs, other database entry activities (specialized department functions).
The candidates profile:
Education: * Minimum: Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent * Desirable: Advanced Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology) or equivalent.
Languages: Fluent English required (oral and written). Good skills in site (local) language desired (oral)
Experience: * Regulatory experience preferred, 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. * 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. * Effective planning, organizational and interpersonal skills. * Reasonable approach to risk assessment. * Excellent written/spoken communication and negotiation skills. * Computer literacy
For further details please contact Beata Arciszewska: email: firstname.lastname@example.org tel: +41435088640