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Postdoctoral Scientist 2 - ye

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Exton, PA

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Job Description: DSM Biomedical develops novel materials-based solutions to meet the present and future needs of the medical device industry. The companyu2019s product portfolio includes coatings, drug delivery platforms, mechanical devices, and a wide range of biomedical materials that enable the replacement, repair, enhancement and the regeneration of tissue and organ functions in the body. Its novel materials-based solutions are designed to meet the needs of the medical device industry. The biomedical market is highly innovative and dynamic. DSM Biomedical is organized in several business units around a combination of technological platforms. These business units are regionally anchored and serve a global customer base. As a partner DSM Biomedical must be pro-active in understanding the needs of the customer and end-user (physician, patient) within the biomedical context. For continued growth and sustainability, new products are continually developed. Scientists are proactive participants and/or leaders in cross-functional teams that may coincide with daily production. At times, Scientists will assist or perform a variety of roles and functions. Primarily, Scientists work independently. Job Content a)Key Areas of Accountability / Responsibility u2022Independently plan, prioritize, and conduct synthesis and testing experiments to advance developmental projects through chemical synthesis, formulation development and characterization u2022Leads R&D efforts in development projects as a technical expert or technical lead u2022Establishes standard operating procedures for chemical processes of new products u2022Designs experimental work and test protocols required to evaluate parameters of new and existing chemical products and processes u2022Leads R&D contributions in the scale-up and qualification of new manufacturing processes u2022Generates process routers, drawings, and other written documentation in accordance with GMP requirements to support commercial manufacturing (e.g. routers, drawings, NCMR, IDP) u2022Creates and maintains project documentation (e.g. Design History File, PMP Documentation) u2022Interfaces with internal and external parties active in product and process development, product testing and commercialization u2022Authors reports, internal/corporate technical documentation, and external scientific publications u2022Communicates results and impact with project directors, R&D management and business leaders u2022Prepares technical documentation for grant applications and regulatory documents u2022Reviews and approves technical documentation for products and processes u2022Develops a comprehensive understanding of intellectual property through submission of invention disclosures and supporting legal through office action responses u2022Maintains a detailed laboratory notebook and accord records according to GLP guidelines u2022Actively participates in establishing safety-oriented protocols u2022Performs other duties as assigned by the supervisor b) SHE & Security u2022It is the responsibility of each employee to work in a safe and responsible manner in order to create an injury-free and incident-free workplace u2022Complies with all job-related safety, security and other training requirements u2022Report any SHE and Security incidents (including observed risks) to management u2022Comply with DSM Life Saving Rules Complexity of the job u2022Individual contributor in multi-functional Development teams u2022Interact with various internal and external disciplines u2022Lead the testing and development of products, processes, and technologies from idea phase through transfer to running business u2022Assist in projects delivered on time and within project budget Knowledge and educational level u2022PhD in Science, Technology or equivalent (e.g., chemistry, polymer chemistry/physics, materials science, chemical engineering, surface-physics, mechanical engineering, biomaterials, etc.) u2022Know-how of operating in the context of the Medical (Device) Industry with regard to Quality System Requirements (e.g., ISO13485, cGMP) and Regulatory Issues Required level of experiences u2022PhD with experience in polymer product/process/application development engineering (e.g., material synthesis & purification, material processing & characterization, manufacturing protocol development) in the biomedical field u2022Highly developed skills working in a multi-disciplinary (Quality Systems governed) working environment u2022Advanced project & task management skills u2022Advanced computer literacy (e.g., MS Word, MS Excel, MS Outlook, etc.) u2022Ability to effectively communicate internally and externally at a technical level; proven ability to maintain effective customer relations at project/program level u2022Self-starting and responsible work attitude with a strong drive for results u2022Creative problem-solving skills u2022Strong individual contributor to group efforts, actively seeking to assist team members in accomplishing tasks and leading new initiatives

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