Tiger BioSciences LLC
Senior Research Scientist at Tiger BioSciences LLC. This role leads research initiatives and drives the development of new products through expert scientific knowledge. The position includes managing project schedules, design of experiments, process development, project budgets, and successful project completion.
Responsibilities
Develop and execute research projects from product concept to market launch with a focus on innovation in human cells, tissue products (from cadaveric or live donation), medical devices, and biologics. Lead comprehensive research projects based on literature reviews, project execution, data analysis, and verification of applicable standards and regulations to ensure successful research development outcomes. Manage and mentor Research Scientists and Associates to ensure studies are executed within project scope, providing scientific expertise and operational support. Track and report research project progress, ensuring milestones are achieved and communicated to leadership and stakeholders on a weekly basis. Work independently on complex research projects and exercise independent thinking and judgment without established protocols when appropriate. Design and execute a variety of scientific experiments related to research projects by generating, collecting, evaluating, and interpreting statistically significant data for decision-making and product launches, using in vitro and in vivo assays. Collaborate with the Research Manager to develop strategic project plans and set research priorities. Develop guidelines, operating procedures, forms, protocols, reports, statements of work, presentations, verifications, qualifications, and other research project documents. Author and review manuscripts and white papers for publication and provide the marketing team with scientific data and insights. Maintain the budget and promote general operational efficiency for assigned research projects. Establish working relationships with vendors to source testing, equipment, supplies, materials, or other resources. Implement quality assurance practices in the design and execution of project activities. Support Project Engineers in scaling manufacturing processes and resolving manufacturing issues. Carry out general laboratory, equipment, and material tracking and maintenance of department resources. Engage with key stakeholders and cross-functional teams to align research projects with organizational goals and expectations. Maintain working knowledge of applicable regulations and standards (FDA 21 CFR 1271, FDA 21 CFR 820, AATB standards, ISO standards, cGMP/CGTP, and internal policies). Maintain acceptable attendance and punctuality, and complete tasks within defined timeframes. Flexible to work outside normal hours with advance notice when necessary. Skills
Strong organizational, multitasking, and detail-oriented abilities with the ability to meet tight deadlines. Excellent verbal and written communication skills for effective collaboration and complex scientific discussions. Ability to work independently or as part of a team, adapting to changing project requirements. Advanced troubleshooting skills with a solution-oriented approach to technical challenges. Strong analytical abilities, proficient in statistical software (e.g., GraphPad Prism) and Microsoft Office Suite (Excel, Word, PowerPoint). Experience planning and executing experiments using complex laboratory instruments and software. Flexible and responsive to changing priorities; highly self-motivated with a focus on quality and precision. Ability to travel for company meetings within the United States. Qualifications/Requirements
Doctoral degree in a scientific discipline with 5 years of post-doctoral experience plus 3 years of industry experience. Master’s degree with a thesis in a scientific discipline with 7 years of industry experience may be substituted to meet doctoral degree requirements. At least 4 years of project management experience. At least 5 years of research & development experience. Experience in technical writing with contributions to peer-reviewed manuscripts, technical reports, and grant submissions. Experience using complex statistical software (e.g., GraphPad Prism). Experience in tissue banking is preferred. Clearance of favorable background investigation required. Seniority level
Mid-Senior level Employment type
Full-time Job function
Other
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Develop and execute research projects from product concept to market launch with a focus on innovation in human cells, tissue products (from cadaveric or live donation), medical devices, and biologics. Lead comprehensive research projects based on literature reviews, project execution, data analysis, and verification of applicable standards and regulations to ensure successful research development outcomes. Manage and mentor Research Scientists and Associates to ensure studies are executed within project scope, providing scientific expertise and operational support. Track and report research project progress, ensuring milestones are achieved and communicated to leadership and stakeholders on a weekly basis. Work independently on complex research projects and exercise independent thinking and judgment without established protocols when appropriate. Design and execute a variety of scientific experiments related to research projects by generating, collecting, evaluating, and interpreting statistically significant data for decision-making and product launches, using in vitro and in vivo assays. Collaborate with the Research Manager to develop strategic project plans and set research priorities. Develop guidelines, operating procedures, forms, protocols, reports, statements of work, presentations, verifications, qualifications, and other research project documents. Author and review manuscripts and white papers for publication and provide the marketing team with scientific data and insights. Maintain the budget and promote general operational efficiency for assigned research projects. Establish working relationships with vendors to source testing, equipment, supplies, materials, or other resources. Implement quality assurance practices in the design and execution of project activities. Support Project Engineers in scaling manufacturing processes and resolving manufacturing issues. Carry out general laboratory, equipment, and material tracking and maintenance of department resources. Engage with key stakeholders and cross-functional teams to align research projects with organizational goals and expectations. Maintain working knowledge of applicable regulations and standards (FDA 21 CFR 1271, FDA 21 CFR 820, AATB standards, ISO standards, cGMP/CGTP, and internal policies). Maintain acceptable attendance and punctuality, and complete tasks within defined timeframes. Flexible to work outside normal hours with advance notice when necessary. Skills
Strong organizational, multitasking, and detail-oriented abilities with the ability to meet tight deadlines. Excellent verbal and written communication skills for effective collaboration and complex scientific discussions. Ability to work independently or as part of a team, adapting to changing project requirements. Advanced troubleshooting skills with a solution-oriented approach to technical challenges. Strong analytical abilities, proficient in statistical software (e.g., GraphPad Prism) and Microsoft Office Suite (Excel, Word, PowerPoint). Experience planning and executing experiments using complex laboratory instruments and software. Flexible and responsive to changing priorities; highly self-motivated with a focus on quality and precision. Ability to travel for company meetings within the United States. Qualifications/Requirements
Doctoral degree in a scientific discipline with 5 years of post-doctoral experience plus 3 years of industry experience. Master’s degree with a thesis in a scientific discipline with 7 years of industry experience may be substituted to meet doctoral degree requirements. At least 4 years of project management experience. At least 5 years of research & development experience. Experience in technical writing with contributions to peer-reviewed manuscripts, technical reports, and grant submissions. Experience using complex statistical software (e.g., GraphPad Prism). Experience in tissue banking is preferred. Clearance of favorable background investigation required. Seniority level
Mid-Senior level Employment type
Full-time Job function
Other
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