Senior scientist providing technical support for commercial and pilot laboratory operations at Elwood, Kansas monoclonal antibody manufacturing facility.
Responsibilities
Partner with Manufacturing, Development, and Quality teams to execute technical and development studies, investigations, validation activities, and technical transfer programs.
Collaborate with cross-functional teams to identify risks, sources of variability, improvement opportunities, and value engineering opportunities to maximize project return and technical success.
Apply scientific and statistical analysis tools to improve process understanding, ensure manufacturing processes remain capable and in a state of control, and identify opportunities for process improvement.
Participate in the design, development, execution, commissioning, qualification, and validation of major projects.
Support project scope definition, development and analysis of design options, establishment of user requirements, equipment selection, and commissioning and qualification activities.
Requirements
Bachelor’s degree in Bio/Pharmaceutical Technology, Microbiology, Engineering, or a related discipline
Nice to have: MSc or PhD in Bio/Pharmaceutical Technology, Microbiology, Engineering, or a related discipline
Nice to have: 5+ years in Biotechnology or Pharmaceutical industry
Nice to have: Experience with commercial monoclonal antibody or recombinant protein manufacturing processes
Lead medicinal chemistry initiatives within multidisciplinary teams, driving design, synthesis, and optimization of small molecules for animal health drug discovery.
Responsibilities
Drive the design and optimization of novel small molecules
Lead medicinal chemistry initiatives within multidisciplinary teams
Serve as a key medicinal chemistry figure on multidisciplinary project teams
Direct synthetic chemistry efforts with external CROs and internal partners
Leverage cutting-edge drug discovery technologies
Requirements
PhD in Medicinal Chemistry, Organic Chemistry, or a related scientific discipline
Nice to have: postdoctoral experience
Nice to have: modern drug discovery technologies such as DEL, computational chemistry, or AI/ML-enabled molecular design
Nice to have: strong track record of advancing small-molecule discovery programs toward preclinical development
Nice to have: prior research experience in the animal health industry
Senior CQV Engineer leading validation lifecycle activities for bioprocessing equipment and facility systems in a manufacturing environment.
Responsibilities
Author, review, and execute key validation deliverables (VMPs, URS, DQ, FAT/SAT, IQ/OQ/PQ) using ISPE risk-based verification approaches in full compliance with EU GMP
Serve as the on-site technical SME during internal quality audits and external regulatory agency inspections
Lead the qualification and validation of critical upstream and downstream bioprocessing equipment, facility systems, and CIP/SIP cycles
Oversee CQV and monitoring for critical utility systems (WFI, PW, Clean Steam, Process Gases) and lead technical root-cause investigations
Direct cleanroom classification and airflow smoke studies, and manage large-scale thermal mapping for cold rooms, freezers, incubators, and warehouses
Requirements
Bachelor’s degree in engineering, life sciences, or a related technical discipline
Nice to have: strong command of risk-based verification approaches
Nice to have: hands-on qualification experience with bioreactors, fermenters, single-use technologies, and autoclaves
Nice to have: proven diagnostic and root-cause troubleshooting capability
Nice to have: proficiency in environmental tracking and thermal validation hardware/software
Skills
Global Engineering Advisor – Facilities & Utilities
Global subject matter expert for facilities, utilities, and HVAC systems, providing engineering guidance for global capital projects and technical support across manufacturing, R&D, and distribution sites.
Responsibilities
Provide global engineering guidance for clean and black utility systems, HVAC, and environmental control systems across the enterprise.
Advise global project teams on the design, commissioning, qualification, and lifecycle management of facility and utility infrastructure.
Evaluate existing systems to identify compliance or reliability gaps and develop practical action plans to support business continuity.
Establish standard design approaches and technical standards to strengthen engineering practices and Community of Practice across the network.
Partner with Quality and Validation teams to ensure systems align with cGMP, data integrity, and inspection-readiness expectations.
Requirements
Bachelor’s degree in engineering, science, or a related technical discipline
Gestionar ventas consultivas del portafolio Pet Health en hospitales, clínicas, farmacias veterinarias y distribuidores directos e indirectos, con enfoque en generación de demanda y cumplimiento de metas de ventas del territorio.
Utilizar herramientas de gestión de clientes, planificación de campo y forecast por cliente y SKU para priorizar cartera, programar visitas y maximizar el valor de las cuentas asignadas.
Presentar información técnica y comercial sobre características, beneficios y diferenciadores del portafolio, y promover su adopción con clientes clave del canal veterinario.
Ejecutar planes de marketing y trade marketing, apoyar iniciativas de cuentas clave y colaborar con el supervisor en planes de ventas mensuales, trimestrales y anuales.
Recopilar información de mercado y competencia, colaborar con los equipos comercial y técnico, y completar en tiempo y forma las actividades administrativas, de cumplimiento, ética, seguridad y gastos del puesto.
Requirements
Licenciatura en Medicina Veterinaria y Zootecnia o carrera administrativa; título o cédula profesional.
Nice to have: Habilidades de negociación
Nice to have: Red de contactos en la industria veterinaria
Studio Manager Part TimeNewBODYBAR Pilates - Naperville · Exton, US