强生-研发职位：Scientific Director, Small Molecule API
This Scientific Director position is a key function within the scientific leadership of Pharmaceutical Development and Manufacturing Sciences (PDMS) of the Janssen China R&D with primary responsibility for managing strategic and day-to-day Small Molecule Active Pharmaceutic Ingredient (API) projects and specifically for this function, overseeing development activities performed at external CRO and CMO partners in China.
The Scientific Director has a shared responsibility for developing and realising the scientific vision for the organisation, strengthening the scientific cability of the China PDMS team within the Small Molecule API space to meet project deliverables and to accelerate timelines, consistently meeting customer and business partner requirements and supporting scientific and technological innovation.
Also responsible for providing scientific leadership in support of PDMS China and API Small Molecule activities at external partners, specifically in China, both with a project focus and also managing/facilitating interactions between stakeholders within PDMS, Discovery and Operations, including multi-disciplinary and multi-site groups, internal resources and external partners.
The main requirements of this role are the following:
Provide oversight and on-site supervision of development activity at external process R&D teams, including responsibility for project and resource allocation in collaboration with the management team of the CRO in question.
Develop and implement PDMS SM API organizational growth plan in China to under the global and local PDMS leadership. Advises Janssen and CRO management of resources, facilities and equipment required to accomplish the assigned tasks. Ensures availability of adequate materials. Recommends and justifies the purchase of capital equipment. Is responsible for long range planning. Organises required budgetary information.
Accountable for the execution of projects allocated to the team and for ensuring the proper recording of information. Ensures that records and raw data are properly retained. Summarizes, interprets, and reviews data.
Ensures the proper and timely preparation of technical reports, manuscripts, and other documents. Consistent with company policy, publishes work in scientific journals. Must have good writing skills.
Effectively applies state-of-the-art scientific knowledge. Demonstrates considerable knowledge/expertise outside of own field, especially in bridging disciplines. Introduces new approaches to the solution of problems.
Must be able to lead teams as needed and assume a scientific leadership role and establish priorities, checkpoints, and time frames for all aspects of work and projects to achieve adequate progress.
Keeps abreast of current scientific and technological developments via broad coverage of the scientific literature, and by interacting with outside experts. Establishes and maintains outside expert contacts. Seeks and utilizes the advice of expert scientists and outside consultants to guarantee efficient and successful projects. Ensures application of all relevant literature search methodologies to drive current projects and to support the development of new ideas.
Trains and directs laboratory personnel at external partner. Delegates work assignments effectively. Strives with supervisee and external partner management to achieve: high level of performance evaluation and development, open communication and mutual respect.
Participates in discussions at management and research meetings, thereby sharing information, knowledge, ideas, and judgement to guide and help establish valid strategic and scientific directions. Contributes to the formulation of goals of own division, both overall and specific, through established forums and own initiative.
Ensures full attention to oversight of GMP aspects at level appropriate to the activity in question, and in collaboration with (and guided by) Quality organisations of both Janssen and the external partner.
Education/special knowledge/skills/experience:
This function will require the following minimum entry requirements: a Ph.D. degree with > 15 years of experience (including postdoctoral studies), within the pharmaceutical and/or fine chemical industries in a development environment, with exposure to early and late development, filing and launch.
Experience in leading a technical team and initiating and managing external partner activity is essential and experience of the manufacturing environment is a plus, ideally in the form of post-approval support and troubleshooting.
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