This position is responsible for providing engineering support and owns multiple systems, processes, or areas. This position will primarily provide technical support of clean utilities and HVAC operations supporting a biologics production facility. This work includes working independently and with Manufacturing Operations, Quality, Outside Contractors, site IT and Manufac

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 Nuclear Med Technologist prepares and administers radiopharmaceuticals as well as other medications to patients and performs the diagnostic study per physician orders. Essential Functions Administers radiopharmaceuticals and medications for patient imaging and therapeutic procedures. Processes data and enhances digital images using advanced computer technology. Provid

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

The Senior Director, Medical Affairs, Parenteral Nutrition (PN) is a critical role as this individual serves as the lead for the US PN Medical Affairs team and is responsible for developing and executing the US Medical Affairs strategy. This individual also collaborates closely with the Global business unit (BU) and the regional marketing organization to identify US nutri

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

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

This position is sign on bonus eligible FT / Schedule is 7 nights on 7 nights off. Assists the registered pharmacists in performing technical duties related to the preparation and distribution of various oral and intravenous medications. Duties are performed under the supervision of a registered pharmacist. Essential Functions Fills and delivers medication orders for all

Under the direction of the Director of Pharmacy, this position fills orders for parenteral and enteral medications, monitors patient drug therapies and provides drug information. Supervises and directs support personnel. Responsible for the procurement storage, dispensing, supervision and management of all legend and non legend drugs for the hospital and shall maintain co

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

Site Name USA Pennsylvania Upper Providence, GSK House, Switzerland Zug, USA Massachusetts Waltham, USA North Carolina Durham Posted Date May 16 2024 Purpose Ensure the development of appropriate Precision Medicine and Digital Health regulatory strategy(s) and their execution for assigned precision medicine and digital health asset(s) supporting across the GSK therapeutic

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

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