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From IND applications through commercial scale production, we provide formulation and compounding, fill-finish, and optional lyophilization services for a wide variety of liquid injectables. Join BioTechnique and help create the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe.
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Facilities Technicians perform a variety of skilled work in the maintenance and repair of facilities and equipment at our pharmaceutical manufacturing site in York, PA. This position offers an excellent opportunity for someone who enjoys being hands on and problem solving, with a mechanical aptitude, strong work ethic, attention to detail, and a willingness to learn and grow within the organization.
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Masters degree in Pharmaceutical Science or related scientific field and minimum 8 years experience in pharmaceutical formulation and product development. PhD in Pharmaceutical Science or related scientific field and minimum 3 years experience in pharmaceutical formulation and product development.
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Advises on the formulation of new or revised policies ensuring they meet the Agency's needs and are consistent with policy writing standards and considerations (e.g., active voice, ease of implementation, meeting Agency priorities (e.g., burden reduction, localization, diversity, equity, inclusion, and accessibility (DEIA.
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Policy Formulation & Clearance. The Mid-level Management & Program Analyst supports the Policy Division in the USAID Bureau for Management's Office of Management Policy, Budget, and Performance and performs the following duties throughout the operational policy lifecycle.
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Ensures that all work is carried out in compliance with company Safety Policies, Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs) Responsible for maintaining all manufacturing equipment including formulation, filling and packaging equipment, and plant utility systems including boilers, air compressors, heating, ventilation and air conditioning systems (HVAC), Water for Injection (WFI), and general upkeep of the physical plant including clean rooms.
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Extensive expertise in every aspect of the creative design journey, encompassing trend exploration, design strategy formulation, concept generation, and proficient execution throughout the manufacturing process.
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General or advanced knowledge in thermal analysis and materials characterization techniques including FTIR, DSC, TGA, GC/MS, rheology, including formulation chemistry and interfacial science and coatings.
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Participate in the development, formulation, modification, and implementation of department policies, standards, regulations, and general operating guidelines and procedures associated with EMS delivery.
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Responsible for entering into negotiations with suppliers and trade partners by reviewing terms and conditions, establishing pricing, contract formulation, and any supplier management conditions affecting the division.
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Assist in the formulation of targets for representatives. Monitors the scheduling and registration process assessing and evaluating Seamless Access Representative’s verbal and written communication skills (including good voice quality, good diction and articulation), customer service, accuracy, call-waiting time, dropped calls and response time to increase revenue, reduce costs and improve service quality.
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The formulation scientist will work closely with downstream and analytical scientists to analyze biochemical and biophysical properties for biopharmaceutical products. Perform UF/DF, HPLC/UPLC, CE, MFI, Osmolality, viscosity, solubility, DLS, and other biophysical techniques for formulation and for characterization of proteins in development.
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Mosaic teams provide comprehensive, end-to-end discovery services, including program assessment and strategy development; program management; antibody discovery and optimization; protein production, purification, and characterization; protein engineering; biochemical and cellular assay development; formulation, stability and developability studies; bioanalytical (PK and PD) assay development; and candidate-validating pharmacology.
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The purpose of this position is to perform tasks and operations relevant to the bulk formulation and/or filling operations required for sterile production of liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing.
$20 - $24 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Participate in unit, departmental and hospital committees for formulation of nursing and hospital policies and procedures. Participate in unit, departmental and hospital committees for formulation of nursing and hospital policies and procedures.
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formulation job
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