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Perform contract development services, including formulation development, analytical development, process development and support of GMP product manufacturing programs for recombinant proteins and peptides. Apply biopharmaceutical principles to develop protein formulations and analytical methods. Qualify, validate and transfer of analytical methods for HPLC, CE, immunoassays; SDS PAGE, qPCR, UV,
Posted 1 day ago
This position is responsible for developing and maintaining detailed component and raw material plans to support production demands. This position is also responsible for planning, procuring and controlling all material specific to the assigned products. Develop component and raw material plans to enable successful completion of the manufacturing plan. Maintain adequate levels of material in suppo
Posted 2 days ago
Responsible for quality oversight of incoming raw materials, manufacturing floor operations, facility/utility qualification and routine support, and QC laboratory investigations. This position will provide a broad range of quality oversight for activities that support bulk drug substance manufacturing. This position will be responsible for review and approval of procedures and methods supporting a
Posted 9 days ago
The Senior Healthcare Representative is a promoted representative level position and is responsible for selling Pfizer's product portfolio to the highest value customers within a district to include physicians, accounts & medical groups. The SHR plays a critical role in increasing Pfizer's brand with high value customers by developing an insightful assessment of the customer and the ov
Posted 3 days ago
Job Summary (Briefly describe what the position was created to accomplish.) Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Conducts laboratory experiments in support of biopharmaceutical development and process development including running electrophoresis gels, HPLC’s, etc. and preparing buffers. Norma
Posted 9 days ago
Responsible for quality oversight of incoming raw materials, manufacturing floor operations, facility/utility qualification and routine support, and QC laboratory investigations. This position will provide a broad range of quality oversight for activities that support bulk drug substance manufacturing. This position will be responsible for review and approval of procedures and methods supporting a
Posted 9 days ago
Role Description The US Biosimilars Account Manager (BAM) is responsible for engaging key hospital and clinic accounts at the regional/local level to • Frame opportunities and challenges through a customer centric lens • Act as the owner of a strategic plan for key accounts and set goals for all account level initiatives and strategies • Deploy existing and newly developed resource
Posted 10 days ago
This position is for a 2 week cycle, night shift with every other weekend off. Coordinate and perform cGMP manufacturing operations for biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products with the highest quality. Execution of procedures for microbial manufacturing without minimal supervision & provide work direction to less experien
Posted 9 days ago
This position is for a 2 week cycle, night shift with every other weekend off. Coordinate and lead cGMP manufacturing operations for manufactured biopharmaceutical products. Ensure safe and effective use of material, equipment and time while manufacturing products at high quality levels. Lead team of peers in execution of microbial fermentation, purification or support areas of manufacturing usin
Posted 9 days ago
This position is for a 2 week cycle, night shift with every other weekend off. Coordinate and perform cGMP manufacturing operations for biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products with the highest quality. Assist in execution of procedures for microbial manufacturing, purification, or support area of manufacturing using SOP's
Posted 9 days ago
The Maintenance Manager is responsible for ensuring equipment and systems are maintained and fit for use in a cGMP biologic drug substance manufacturing site. The Manager oversees day to day maintenance operations including planning and scheduling, coordination of work order execution, troubleshooting and problem solving, and ensuing quality and completeness of maintenance documentation for cGMP m
Posted 9 days ago
Provide leadership and coordination of company financial planning and budget management functions including analysis of budget to actual results. Assist Senior Director, Finance in preparing, updating and coordinating Budgets, Forecasts, Analysis and review of data. Assist Controller to ensure company accounting procedures are followed and conform to Generally Accepted Accounting Principles. Respo
Posted 9 days ago
Job Summary The Manager has overall responsibility for the site’s Health, Safety, and Environment (HSE) program. The includes maintaining compliance and managing HSE improvements. The Manger facilitates HSE governance and execution of HSE activities associated with biotechnology laboratories and manufacturing. The head of HSE promotes positive safety culture and behaviors. Coordinates with o
Posted 9 days ago
Manages the Quality Engineering department responsible for QA team supporting Facilities and Engineering and Validation, change management, technical document review and approval, review and resolution of deviations, review and approval of CAPAs, SOP review and approval, supports client and regulatory audits, trains and mentors staff. Responsible for Quality Engineering staff located at KBI Biopha
Posted 9 days ago
Receives, stores, and distributes materials, tools, equipment, and products within establishment by performing the following duties Maintain shelf life and lot controls for Boulder Stockroom, keeping accurate inventory levels and performing year end physical counts. Dispense GMP raw materials and components for use manufacturing using SOP’s, solution prep documentation and batch records. R
Posted 9 days ago
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