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- Irvine, CA

The candidate is responsible for expeditiously developing and processing raw material and product documentation to meet quality requirements within timelines established for product launch and/or timely project completion.The Master Specifications and Documentation department interacts with various Pharmaceutical groups within the organization and departments such as Quality, Global Pharmaceutical Technology, Regulatory Affairs, Operations, Manufacturing (all sites), Procurement (Sourcing),....


The specialist will work with a team of medical information professionals to capture unsolicited medical inquiries from health care professionals, consumers, and corporate business partners. Also, research and respond to requests for scientific/medical information using various search and retrieval techniques and medical literature database (product label, published and unpublished studies) to develop a medical/scientific response that is accurate, fair balanced, complete and delivered in a....

- Lancaster, SC

We are looking for an Associate Brand manager to support the planning and development of annual marketing and business plans that align with organizational goals and objective, aiming to achieve sales growth, profit margins and market share targets. Roles and Responsibilities:Assists with the management of the brand portfolios to maximize long-term sales and profit; develop and execute portfolio strategy to build long-term brand health.Assists Brand Manager with the development of Global brand

- Edgewood, MD

We are looking for a Quality Control Chemist to work in a cGMP laboratory who will operate laboratory instrumentation, troubleshoot and generate/revise SOPs and test methods. General Responsibilities:The Quality Control Chemist (QCC) reports to Quality Control (QC) Management.The QCC will stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the Quality Control Chemistry Laboratory complies in the areas of analytical applications, release....


The Associate will be responsible for supporting CTM/OSL and ensuring that all assigned clinical study(ies) are running on time and on budget and are completed in compliance with all relevant laws, regulations, and regulatory guidelines as well as all policies and procedures. Requirements: Bachelor’s degree or higher (science degree preferably in science or health-related field) Previous experience of working on a clinical study 1-2 year relevant experience in pharmaceutical industry or CRO....


Summary of the Position: This position is responsible for providing technical support consist of drafting “Ask a Vet” Forum responses for the Technical veterinarian to finalize until the new website is completely in place, overseeing Adverse Event Reports (AERs) by being the first contact for the Customer Service Representatives for any issues, questions or concerns, being responsible for the accuracy of the information contained in the reports, and responding to technical calls and e-mails as


Job Title: Specialty Pharmacy Director Location: Baltimore, MD PRINCIPAL ACCOUNTABILITIES: The position reports directly to the Senior Director of the Pharmacy Evaluation & Oversight and is a critical leadership position within the unit responsible for understanding the specialty marketplace, opportunities for utilization management, and cost containment. The Director of Specialty Pharmacy will interact frequently with the EVP of Medical Affairs, the CEO, and other senior leaders across....


We are in search of a Medical Director who is and actively practicing Board Certified Physician Board certified by the American Board of Psychiatry and Neurology. This is a role where you are directing and coordinating the medical management, quality improvement and credentialing functions. You should be willing to practice clinically ONE day a week. Salary plus 20% bonus or higher We can only consider those who are Board certified by the American Board of Psychiatry and Neurology. Current....


In this role, you will serve as the primary point of contact for all areas of the Supply Chain specific to key customer(s). Manages the flow of materials from inbound ingredient receipt to shipment of finished goods to customers via an optimized inventory approach that supports a 100% ready to execute and >98% service agenda. Ensure success in developing, and continuously improving the tools and processes to achieve these results. Provide analysis and help lead systemization,....


Pharmaceutical company hiring MSLs- Pain and Addiction - Opioids Opening for an MSL in Pain and Addiction : East Coast - CT, NY, NJ, PA (must be located in one of these states) The Medical Science Liaison (MSL) plays a crucial role in Medical Affairs, being part of an exclusive field-based team of medical scientific experts that partner with national, regional, and local key opinion leaders (KOLs). Thus, the MSL has significant responsibility and is expected to provide in-depth scientific,....


Develops and maintains professional relationships with internal and external customers to provide comprehensive medical and scientific support to company initiatives in assigned therapeutic areas. Facilitates information, education, and research activities for physicians and ancillary healthcare professionals regarding current and future therapies in development or commercialized. Works closely with other personnel to ensure information, education, and research needs of healthcare....


EDUCATION/EXPERIENCE: - 1+ years of relevant experience in pharmaceutical industry - Science degree in medical or health-related field - Clinical Trial Support/Clinical Study experience - Work effectively in a team/matrix environment - Handle conflict management and resolution RESPONSIBILITIES: - Ensuring that clinical studies are run on time and budget - Ensure compliance with regulatory guidelines - Management of clinical trial documentaiton - Tracking of various clinical trail resources

- 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,....

- Waupin, WI

Provision of pharmaceutical services for offenders in Wisconsin's correctional system through the Bureau of Health Services Central Pharmacy Service in a manner consistent with professional standards and comparable to services delivered in non-correctional settings. Prepares, fills and dispenses prescriptions for drugs, chemicals and supplies on receipt of a proper order from a prescribing practitioner for an inmate/student. Prepares and fills extemporaneous prescriptions and orders....


Summary of the Position: We are looking for a Manufacturing Operations Manager to manage staff, processes, procedures and policies in effort to meet company goals and objectives, included but not limited to Safety, Quality, Compliance and Company Policies and Procedures. Responsibilities include, but are not limited to overseeing the planning, organizing, managing, controlling and evaluating the day to day operations of the department and area of responsibilities in order to optimize....


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


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....

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