- Eisai, Inc (Charlotte, NC)
- …training, marketing, managed markets, sales/business analytics, etc.)Strong understanding of pharmaceutical manufacturer compliance & regulatory ... to work cross-functionally while adhering to all of Eisai's ethics and compliance standards. Senior Neurology Account Specialist (Sr NAS) Responsibilities… more
- Eisai, Inc (San Diego, CA)
- …approved promotional clinical trials, patient access to medication, and regulatory / compliance guidelines.Strong knowledge of key laws and regulations ... and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ... in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based in Raritan, New Jersey. Role… more
- Eisai, Inc (Louisville, KY)
- …approved promotional clinical trials, patient access to medication, and regulatory / compliance guidelines.Strong knowledge of key laws and regulations ... and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... internally and with external parties. Ensure that all employees are in compliance with all contract requirementsSupport the Associate Director Global Strategy and… more
- Merck & Co. (Durham, NC)
- …for the company; uses this knowledge in own work Understands and applies regulatory / compliance requirements relative to their role Basic conceptual knowledge ... with our incredibly high standards of quality and meets all regulatory requirements.- Partnering across our internal manufacturing facilities, external contract… more
- Merck & Co. (Rahway, NJ)
- …vaccines, antibody drug conjugates (ADCs), in addition to others.- --The Senior Specialist , Engineering will serve as a business representative in the FLEx Sterile ... and reports to the FLEx Sterile Expansion Business Lead within Pharmaceutical Operations and Clinical Supply.- Education Minimum Requirements :- Bachelor's degree… more
- Legend Biotech USA, Inc. (Memphis, TN)
- …to healthcare professionals in accordance with Corporate, PhRMA, and OIG guidelines.Strict compliance with all regulatory agencies, state, and federal law is ... a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop...myeloma.Legend Biotech is seeking a Sr. Cell Therapy Account Specialist - Memphis, TN as part of the Commercial… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ... an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Maintenance Specialist as part of the Technical Operations team based in Raritan, New… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ... of multiple myeloma.Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role OverviewThe… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in a fast paced and dynamic, growing environment.Strong understanding of regulatory and compliance requirements.Excellent oral and written communication ... entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This ... Essential Functions Reviews all manufacturing and support records to certify compliance with specifications and procedures Releases product based on Quality… more
- Merck & Co. (Rahway, NJ)
- …of the current IT division that provides support to the Pharmaceutical Research and Development (R&D), Supply Chain (Manufacturing), Marketing (Human Health) ... collaborate with other SAP and non-SAP Business Areas, Digital Manufacturing Division, Compliance , our Research & Development Division Value Team, GSMG etc. Hold… more
- ICONMA (Newark, CA)
- … regulatory issues affecting own area of work. Notifies manager of regulatory compliance questions and issues. Follows Environmental, Health and Safety (EH&S) ... storage. Processes document workflows, reviewing documents for correct format and compliance with company templates. Scans records and verifies accuracy and… more
- Actalent (Camarillo, CA)
- Description: Summary The Regulatory and Compliance Specialist is responsible for initial new product assessment, confirming authorized distributors, NDC ... Participates in, and provides support as needed to other regulatory affairs, regulatory compliance activities...Education: Bachelor's degree or 5 years or more of pharmaceutical regulatory experience required RAC ( Regulatory… more
- Stryker (Cary, IL)
- …More information is available at www.stryker.com We are currently seeking a **Staff Regulatory Affairs** ** Specialist ** **,** ( ** Pharmaceutical Products** ) ... for sales, management, and leadership teams. **What you will do** As the **Staff Regulatory Affairs Specialist ** , you will provide information used to evaluate… more
- Catalent Pharma Solutions (Greenville, NC)
- ** Pharmaceutical Manufacturing Specialist ** **Position Summary** Catalent is a global, high-growth, public company, and a leading partner for the ... Monday - Thursday, 4 PM - 2:30 AM The Pharmaceutical Manufacturing Specialist has a primary focus...a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer… more
- Catalent Pharma Solutions (Somerset, NJ)
- …Friday,** **8:00AM - 5:00PM** Catalent Pharma Solutions in Somerset, NJ is hiring a Senior Regulatory and Compliance Specialist for the Compliance Group. ... The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining...industry in Quality Assurance, Pharmaceutical Manufacturing, or Compliance + Knowledge of US FDA regulatory … more
- Guthrie (Sayre, PA)
- …training in the area of infectious disease COMPETENCIES: The clinical specialist must demonstrate growth and development of knowledge required to assess ... appropriate information needed to identify each patients requirements and to provide the pharmaceutical care needed, appropriate to the age of the patient and in… more
- Catalent Pharma Solutions (Harmans, MD)
- ** Regulatory Affairs Specialist ** **Position Summary** Catalent Pharma Solutions is hiring a Regulatory Affairs Specialist . The Regulatory Affairs ... the regulatory aspects and climate that would affect proposed activities. The Regulatory Affairs Specialist will provide regulatory support for the… more
