This position is on 2 2 3 shifts, 7p 7a. The Sr. Manufacturing Associate I/II MFG Support is responsible for the execution of production activities of Media and Buffer preparation within a GMP environment. The Sr. Manufacturing Associate I/II Support must follow the instructions depicted in SR's (Media / Buffer Solution Records), SOP's and forms. Additionally, must ensure

Primary r esponsi bility writing and editing detailed technical proposals and project plans for KBI services . Proposals cover contract process development , analytics, and GMP manufacturing of biotherapeutics. Collaboration with cross functional teams including Business Development, Process Development, Analytical Development, Manufacturing, and Program Management teams

Please Note This position operates on a night shift 2 2 3 schedule and will be eligible for shift differential. Position Summary The Senior Manufacturing Associate I/II (Sr. Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Sr. Manufacturing Associa

This position operates on a 2 2 3 schedule, with 7 00 pm 7 00 am shifts. The Manufacturing Supervisor leads a team of manufacturing associates to perform upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Supervisor will plan, assign, and monitor daily tasks to ensure timely "Right First Time" execution

Perform the day to day management and distribution of a rapidly growing library of biologics samples. Will be responsible for checking in, registering, and aliquoting new samples, maintaining database and Access/Excel inventories, and labeling and distributing outgoing samples. Will work closely with basic automation (i.e. Tube Cappers, barcode readers, automated liquid h

The Operational Excellence (OpEx) Senior Specialist or Manager will support the site's portfolio of continuous improvement initiatives, activities, and high value projects. The Sr OpEx Specialist will manage several projects concurrently, coach leaders through the successful execution of improvement events, and capture significant sustained value for our customers. The Sr

Assist with and support execution of routine procedures within the manufacturing area. Position Responsibilities Order and stock general supplies in the manufacturing production areas Wash glassware/labware and clean equipment Perform GMP cleaning of suites as required Maintain records to comply with regulatory requirements, cGMPs, and SOPs The responsibilities of this po

Identifies, evaluates, develops and closes new customers and expands business at existing customers. Identifies and assists in progressing biopharmaceutical business opportunities including new scientific and strategic partnerships, collaborations, licensing opportunities, joint ventures and alliances. Establishes and implements appropriate development strategies to suppo

The Senior Manufacturing Associate I/II is responsible for performing upstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Senior Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted "Right First Time" (RFT) following Good Manufacturing Practices (GMP), Good Document

This position is on a 2 2 3 shift, with the hours 7p 7a. The Sr. Manufacturing Associate I/II Downstream is responsible for the execution of production activities for early and late phase Cell Culture programs within a GMP environment. The Sr. Manufacturing Associate I/II Downstream must follow the instructions depicted in SR's, EPR's, BR's, SOP's and forms. Additionally,

This position operates on a 2 2 3 schedule with the hours 7 00 am 7 30 pm. The Manufacturing Assistant position is designed as an introduction to the industry of cGMP manufacturing. This position performs all routine/non routine cleanings and maintains gowning supplies for the locker rooms and gowning rooms at the CMF GMP facility to support continuous manufacturing opera

We are currently seeking a highly motivated and detail oriented individual to fill the role of Inside Sales Sr. Technical Lead. This position will report to the Associate Director, Contracts, Inside Sales, and Analytics and will be responsible for prospecting, lead generation, and lead management. Through effective prospecting, they will build and expand the corporate cli

The Supply Chain Operations Analyst (Intern) is accountable for the design and execution of demand planning and order forecasting, supply planning, product deployment and expediting processes and the development and implementation of a stocking optimization model to minimize costs and inventory while delivering on service requirements. Position Responsibility Research and

The Facilities Engineering Department is responsible for all aspects of maintaining the site infrastructure in an active reliable state to support cGMP operations. Facilities Engineering oversees the architectural features of the buildings, Structural/Civil, Biotech process and laboratory equipment and systems, HVAC, Plant and Clean Utility Systems, Electrical Power and L

The Facilities Engineering Department is responsible for all aspects of maintaining the site infrastructure in an active reliable state to support cGMP operations. Facilities Engineering oversees the architectural features of the buildings, Structural/Civil, Biotech process and laboratory equipment and systems, HVAC, Plant and Clean Utility Systems, Electrical Power and L