The upstream manufacturing supervisor will lead associates during the startup and production in the cell culture areas for a new clinical GMP biopharmaceutical facility. The supervisor will coach associates during the commissioning, qualification, and production activities while safeguarding work environments and ensuring cGMP compliant behaviors. Upstream supervisors wil

The manufacturing support manager will oversee the management of the manufacturing support activities in support of the startup and production at a new clinical GMP biopharmaceutical manufacturing facility. The individual will lead the manufacturing support team with the aim of achieving superior quality, safety, productivity and cost objectives. The individual will lead

Responsible for independent problem solving. Specialized in at least one discipline that is directly applicable to the job function. Execute components of a project. Focus on meeting deliverables. Position Responsibilities Develops, leads and supports a team responsible for downstream process development and manufacturing activities. Conceptualizes, proposes and executes

Effectively leads a team within Program Management or large Project Management function, ensures appropriate development and control of related processes and systems. With personal responsibility for a portfolio, the role holder is the primary client account and relationship manager for KBI PMO, driving business delivery and exemplary client service to maximum benefit for

The incumbent will have Operation Excellence / Lean Six Sigma expertise and ideally manufacturing, process development and/or new technology introduction experience. The incumbent will support and manage key Manufacturing continuous improvement initiatives and high value cross functional projects. Incumbent will actively manage several projects concurrently. Job Responsib

Responsible for contributing to the development, maintenance, and continuous improvement of the GMP Training Program. Facilitate projects and training initiatives that drive quality, compliance, and operational effectiveness for the organization. Develop training materials and provide guidance in development and implementation of a consistent training program. Assess new

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

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

Provide calibration, troubleshooting and repair of analytical instruments. Provide calibration, troubleshooting and repair of development instruments used in upstream process development, downstream process development, and analytical development laboratories. Perform and/or coordinate scheduled preventive maintenance on HPLC's, UPLCs, capillary electrophoresis instru

This position will act as AQC group leader, responsible for independent problem solving. Execute components of a project. Focus on meeting deliverables Job Responsibilities Supports product development efforts in the process, formulations, and analytical development areas. Conceptualizes and proposes process development, formulations development and analytical development

The incumbent will support GMP manufacturing operations for late phase and commercial mammalian Cell Culture programs and oversee compliance activities for the department. The individual will support operations during the planning stages by releasing electronic manufacturing logbooks and records, as needed. The employee will support operations during the execution stage b

The downstream manufacturing supervisor will lead associates during the startup and production in the purification areas for a new clinical GMP biopharmaceutical facility. The supervisor will coach associates during the commissioning, qualification, and production activities while safeguarding work environments and ensuring cGMP compliant behaviors. Downstream supervisors

Ownership of the CECL calculation engine for all in scope assets, ensuring alignment with regulatory, audit and model risk management standards and including understanding and proposing improvements to platform configurations and calculation methodologies Coordination with stakeholders and owners of sub functions within the CECL process, including accounting / finance, an

UNC's Department of Pharmacy is an organization of more than 300 dedicated employees with focused attention on caring for patients of the UNC Health Care system. The department is culturally diverse and has a variety of backgrounds, interests, capabilities, and experience. Additionally, the UNC Department of Pharmacy is nationally recognized for excellence in pharmacy pra

Other duties as assigned. Qualifications Minimum Experience/Education Demonstrated possession of the competencies necessary to perform the work. Other Required Qualifications Excellent interpersonal and communication skills. Careful attention to details. Basic knowledge about safely conducting research activities, and using research equipment in the field, laboratory, gro