201-220 of 277 results
Sort By

- Any US State

Position Summary: The Senior Director, CMC Regulatory Affairs will be responsible for providing CMC regulatory leadership and strategy across the organization and to our global partners. The Sr Director, CMC Regulatory Affairs will collaborate with the clinical development team, including the Chief Scientific Officer and drug substance and drug product manufacturers, and others for drug development and manufacturing in the pharmaceutical and biotech industry in accordance with the protocol,....


Although this position is titled QC, it is really a new model launch management position which will handle all quality issues pertaining to new product/model launch. The overall focus of this position will be to support launch activities to assure SQAM documents are created and quality levels meet customer expectations. Manage ECI implementation by communicating all department expectations and schedules. Successful candidates will have over 5 years of experience in related quality and/or....

- South Bend, IN

COMPANY BACKGROUND: A research laboratory that has been manufacturing & distributing a variety of enzymes & cofactors used in basic coagulation research for over 30 years is looking for a Technical Specialist to join their team. Their diagnostics division/sister company provides general purpose & specialty assays to the clinical coagulation laboratory; the laboratory incorporates the research laboratories high purity proteins & reagents into clinical diagnostic kits. POSITION....


This is a neat opportunity! Our client has a food & juice product manufacturing facility in Indiana. They are looking for an experienced Quality Assurance / Food Safety Technician You will be working with all quality assurance and food safety aspects of food processing activities; assist with developing and refining food safety plan for operations, participate directly in continuously improve plan and maintain facility food safety and quality assurance department as a GFSI Practitioner.....

- Philadelphia, PA

Clinical Research Veterinarian position with my world class, stable, northeast based research organization. They require a DVM/VMD degree from an AVMA-accredited veterinary school and a minimum of 1 year of experience in Laboratory Animal Medicine and USDA accreditation within 6 months of employment. In turn they offer the opportunity to be part of a renowned team of researchers and to contribute to the discovery of life improving/saving treatments for a variety of debilitating diseases along....


Pharmaceutical company in need of Director or Senior Director to join the Medical Affairs team. The Medical Director will provide support and expertise in the area of psychiatry either Schizo or Addiction as there are two needs In this newly created and high profile role you will serve as the medical affairs strategic lead for our combination oral schizophrenia treatment that is currently in phase 3 clinical development. The Medical Director is expected to establish key medical strategies for....


SENIOR RESEARCH INVESTIGATOR-Liver diseaseRare opportunity to transition from Academia for a specialist in liver disease research. You would work on interdisciplinary teams, where you will function independently in the execution of the experiments but will need to work collaboratively with other team members. Working independently, you will perform design, optimization and implementation of complex in vitro and in vivo experiments in rodents and NHP, and provide cross-organizational support....

- Philadelphia, PA

SENIOR RESEARCH INVESTIGATOR-TRANSLATIONAL RESEARCHRare opportunity to transition from Academia for a specialist in airway/pulmonary disease research. You would work on interdisciplinary teams, where you will function independently in the execution of the experiments but will need to work collaboratively with other team members. Working independently, you will perform design, optimization and implementation of complex in vitro and in vivo experiments in rodents and NHP, and provide....


Position Overview The Sr. Manager will represent Regulatory Affairs for pharmaceutical development projects and marketed products. Working with manager, responsible for development and communication of global regulatory strategy on R&D project teams. Main Areas of Responsibilities The Sr. Manager Regulatory Affairs will ensure technical accuracy and regulatory compliance of all submissions for which they are responsible and ensures that applications are executed appropriately and submitted


We are currently recruiting for a NASH Medical Director, Medical Affairs within Global Medical Affairs (GMA) and the Chief Medical Office (CMO). Working under the leadership of the Global Therapeutic Area Head, this role develops a comprehensive medical strategy for several products in development to treat Non-Alcoholic Steatohepatitis (NASH). They will work closely with Clinical Development colleagues within Research & Development as well as colleagues within Global Evidence & Value....


Job Category: Research & Development The Senior Clinical Program Leader I3 (Inflammation, Immunology and/or Infectious Disease) is accountable for the operational strategy, planning and execution of the clinical development portfolio up to LIP for the designated Discovery and Translational Area (DTA).You provide the primary interface between the I3 DTA and pRED’s the Clinical Program Execution (CPEX) function in Clinical Operations, oversight for program and study management, line....


Position Overview Plans, directs, and executes product formulation and process development activities in support of development of new products intended for clinical trials and commercialization with focus solid and liquid dosage forms including immediate and controlled/modified release systems. Conducts research in the area of formulation sciences in support of innovative product development both for new chemical entities and life-cycle management of marketed products. Experience in the....


Registered Architect minimum 7+ years' experience in and commitment to healthcare programming/planning/design with a demonstrated ability to develop facility programs and designs in compliance with client needs and industry best practice Strong design, organizational and communication skills Ability to clearly communicate design ideas through freehand sketching and rendering Demonstrate strong organizational, time management, presentation skills and attention to detail Knowledge of....


Information Security Risk Assessment Delivery Lead - Phoenix AZ Must be a citizen or permanent resident of the United States The Information Security Risk Assessment Delivery Lead directs and leads a team of assessors to proactively identify, assess, and communicate the company’s information security risks as a key component of the enterprise risk management program. Independently oversee the delivery of high-quality assessments across a diverse set of technologies, business functions, and....


Information Security Risk Assessment Delivery Lead - Charlotte, NC Must be a citizen or permanent resident of the United States The Information Security Risk Assessment Delivery Lead directs and leads a team of assessors to proactively identify, assess, and communicate the company’s information security risks as a key component of the enterprise risk management program. Independently oversee the delivery of high-quality assessments across a diverse set of technologies, business functions, and....


Summary We are currently accepting resumes for the position of Research Scientist in Analytical R and D/Methods Development and Validation. ResponsibilitiesMust be fully capable of developing analytical methods based on experience, literature search, etc.Design, develop, conduct and/or review experiments including method development and methodtransfer; perform methods validations utilizing typical instrumentation including but not limited to LC,MS, GC, etc.Interpret data from routine and....


Medical Affairs – Fully integrated, global biopharmaceutical company developing innovative medicines for the treatment of central nervous system (CNS) diseases. The company has a diversified commercial product portfolio and a substantial clinical pipeline of product candidates for chronic diseases that include schizophrenia, depression, addiction and multiple sclerosis. In this highly visible leadership role in Medical Affairs, you will work closely with a cross-functional group that includes....


MUST have international tax planning and accounting experience. Supports tax leadership to analyze research, implement and support business structures and strategies that optimize the company's tax profile. Support/lead the preparation and presentation of information to senior leaders to obtain buy in, to update and to ensure ongoing institutional understanding of the business operations from a legal entity, jurisdictional and functional perspective. Additional activities/objectives:Think....


The Director, Clinical Pharmacology acts as the primary clinical pharmacology lead providing clinical pharmacology expertise to a multidisciplinary study team. The Associate Director/Director, Clinical Pharmacology is responsible for clinical pharmacology programs for assigned projects and will be the key expert on all clinical pharmacology & pharmacometrics matters relating to assigned projects. The Associate Director, Clinical Pharmacology will work in close collaboration with different....


Reporting to the Vice President, Drug Development-Generics, the Director, Project Management will use the global PDP (Product Development Process), allied systems & tools, to plan and manage/coordinate resources and activities related to product development and maintenance of business projects throughout Global R&D, and other company organizations. Responsibilities: Responsibilities:Champion and lead projects for new generic product development.Management of project team members from....

201-220 of 277 results