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Support pilot manufacturing of new project introductions and sustaining projects within cGMP workflows utilizing SOPs. Responsible for formulation of liquid components, filling of various liquids, and creating lyophilized product in an ISO cleanroom environment.
$20ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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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.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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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 2 days ago - UpvoteDownvoteShare Job
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Lief Labs is a premier formulation and product development innovator and manufacturer of dietary supplements. This person must comply with current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), Laboratory Safety and any regulatory requirements.
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Ability to maintain compliance in all SOP, cGMP, EHS and other training curriculum as assigned. In this position, you will be responsible for performing operations related to the manufacturing of pharmaceutical products through equipment set-up, operation, clean up and maintenance in compliance with all regulatory cGMP requirements and company policies and procedures.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Process Technician position is responsible for the operation of high-speed equipment used in the production and packaging of BacT/ALERT bottles and/or preparing and formulating the liquid reagents that fill the finished BacT/ALERT bottle in a cGMP compliant manner.
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10+ years Downstream Process Development experience related to biochemical engineering and/or protein biochemistry, scale-up principles, and manufacturing of Biopharmaceuticals (cGMP) The position will require a high degree of autonomy in the discipline and work with colleagues in cell culture, bacteriology, virology, formulation, and bioanalytical science.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Dental Technologies, Inc. is a company specializing in the research, formulation, compounding and packaging of dental, orthodontic and oral pharmaceutical products. Complies with cGMP, EHS guidelines, and all working procedures assigned to the position.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Interface effectively with other scientific disciplines (e.g., Quality Assurance, Analytical Chemistry/DMPK, Process Chemistry, and Formulation Development) Expert knowledge of cGMP compliance, ICH guidelines, compendial standards, and HA regulations pertaining to pharmaceutical manufacturing, method validations, product specifications, stability programs and other QC/AD activities.
$178,000 - $218,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Hires will be responsible for the formulation of bulk liquid and semi-solid dental and oral health care. Familiar with measurement scales, mixing, blending, chemical mills and other formulation manufacturing equipment.
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Bioprocess cGMP experience; harvest clarification, downstream processing, bulk fill, formulation and filling, PUPSIT etc. Bioprocess cGMP experience; harvest clarification, downstream processing, bulk fill, formulation and filling, PUPSIT etc.
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Perform routine production activities such as upstream and downstream processing, purification, and formulation. (Required) Familiarity with cGMP regulations and industry standards for biopharmaceutical manufacturing.
$32 - $34 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Industry giant seeks an experienced Process Development Scientist to develop protein purification processes to be scaled up and transferred into cGMP manufacturing including evaluation of transferred processes, transfer of processes to manufacturing, harvest clarification, normal flow filtration, purification, tangential flow filtration, and product final formulation.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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As a Production Supervisor, you will play a pivotal role in overseeing various production areas including formulation, aseptic filling, inspection, and labeling/packaging. Bachelor's degree or 5+ years of experience in cGMP production, preferably in pharmaceutical manufacturing.
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Clean compounding formulation equipment/vessels, and maintain general cleanliness of area and equipment to ensure optimal operation and aseptic production. Support timely manufacturing of parenteral cGMP products in an aseptic environment including set up, operating, sanitizing, and sterilizing equipment and manufacturing areas; preparing, washing, and sterilizing vials; completing batch calculations, preparation, and formulations.
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