POSITION SUMMARY Responsible for the accurate weighing, checking and verification when mixing specific chemical compounds for product formulation. Performs monitoring of mixing and ancillary support equipment throughout formulation and filling and executes calibrations and preventive maintenance activities. Routinely complies with cGMP's, departmental SOP's and company po

Site Name Cambridge MA, GSK House, Stevenage, Upper Merion, USA Maryland Rockville, USA North Carolina Durham Posted Date Apr 19 2024 Are you looking for a role where you will serve as a key strategic partner representing Global Regulatory activities? If so, this Director of Regulatory Affairs, CMC could be an exciting opportunity to explore. This role will provide strate

Compounder 8 Sanford, NC To manufacture and preweigh bulk batches and receive raw materials. Adhere to HR, S&H policies, respect GMPs (Good Manufacturing Practices), and follow departmental procedures with respect to manufacturing, preweigh, and receiving. Contribute positive results to the bulk department key objectives (QA Index, GCM, S&H, RFT). In this role you will be

Primary Work Address MSRB 1, Suite 301, Research Drive, Durham, NC, 27710 Current HHMI Employees, click here to apply via your Workday account. We currently have an opening for a Research Technician I in the lab of Dr. Cagla Eroglu at Duke University. The Eroglu Lab investigates the cellular and molecular mechanisms that underlie synaptic connectivity in the CNS. Currently

Under the direction of the Director of Pharmacy, this position fills orders for parenteral and enteral medications, monitors patient drug therapies and provides drug information. Supervises and directs support personnel. Responsible for the procurement storage, dispensing, supervision and management of all legend and non legend drugs for the hospital and shall maintain co

You will be expected to work with senior researchers to Develop research concepts related to progression of a respiratory disease, pre clinical and clinical measures of respiratory health, and biomarkers of physiological response. Conduct research studies that combine environmental, mobile health technologies, social, and behavioral factors that impact (positively or nega

JOB DESCRIPTION Make your mark for patients. We're here because we want to build the future and transform patients' lives for the better. At UCB, our people are our experiences and achievements, our passion and drive. That's why we're looking for talented individuals with diverse backgrounds and experiences not just the best and brightest, but those who care about making

Responsible for directing and overseeing microbiological programs and methods activities for processes, instruments and equipment. Ensures the effective use of material, equipment and personnel while developing products and processes at high quality levels. This person is responsible for the aspects of the following programs as directed by management Environmental Monitor

Site Name Durham Blackwell Street, USA Pennsylvania Philadelphia Posted Date Apr 17 2024 Does leading and delivering Chemistry and Manufacturing Controls regulatory strategy interest you? If so, this role may be for you! As Regulatory Affairs Chemistry, Manufacturing and Controls (CMC) Manager, you will be responsible for managing global CMC regulatory activities, from ea

Conduct GLP and non GLP genetic toxicology assays (i.e. Ames, Comet, and micronucleus assays) Maintain and dose cultured cells, including primary cells and stem cells. Perform laboratory maintenance tasks (e.g. material storage and disposal, equipment monitoring/maintenance, etc.). Assist in the maintenance of supply inventories Maintain study books. Handle data (e.g. org

ViiV Healthcare is a global specialty HIV company, the only one that is 100% focused on researching and delivering new medicines for people living with, and at risk of, HIV. ViiV is highly mission driven in our unrelenting commitment to being a trusted partner for all people living with and affected by HIV. Our aim is to think, act, and connect differently through a focus

You are an expert facilitator you open doors, foster communication, and bridge the gap. In this role, you will operate as the subject matter expert on reimbursement, access, and coverage issues affecting the clients product. Educate HCPs and their staff on matters related to reimbursement, access and coverage to facilitate appropriate patient access. You will Analyze acce

M F Business Hours Primary responsibilities for this position include performing tasks associated with method validations and transfers. The analyst will be responsible for ensuring that Seqirus validation samples are tested and reviewed according to quality requirements and results reported are valid, accurate, and documented per applicable regulatory and corporate requi

Responsible for the regulatory review and submission of advertising and promotional materials for all Chiesi Global Rare Disease products in the United States. This position is also responsible for providing input to risk management activities, managing the labeling control process, including generation of new labeling and changes to existing labeling, and submission of l

Responsible for reception area and acts as receptionist for visitors. Assist site leadership in the facility and administrative management of the Leuven, Belgium site. Job responsibilities Maintain office services by organizing office operations and procedures. Place and manage supply requisitions. Coordinate orientation and training of employees. Coordinate receipt and s