CELADON PHARMACEUTICALS PLC  Salary

CELADON PHARMACEUTICALS PLC
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CELADON PHARMACEUTICALS PLC is looking for employees for positions:

laboratory technician

Working hours

  • full-time

Requirements

  • A Bachelor's degree in Chemistry, Biochemistry, or a related field would be desirable
  • experience with laboratory management, equipment maintenance, and inventory control
  • excellent attention to detail and the ability to follow protocols and procedures with minimal supervision
  • working in a laboratory pharmaceutical/healthcare desirable
  • GMP experience desirable
  • BSc in a scientific discipline
  • knowledge of Good Laboratory Practice standards
  • ability to prioritize assignments and work with multiple tasks

Responsibility

  • responsibility for QC sampling of raw material, in-process, API and drug products on-site
  • technical support where requested to QC method development, method validation, method transfer and routine testing in an ISO 17025 laboratory
  • this is an important hire for the business with responsibility for sampling of all on-site raw materials, intermediates, in-process, botanical and API drug substances as well as the co-ordination of samples that are sent to third parties and outsourced partners
  • experience in supporting any laboratory operations including stock control, ordering chemicals, maintenance and cleaning
  • the successful individual will also play a key part in providing technical support to all laboratory processes such as calibration, maintenance and cleaning as well as support to the QC analyst and R&D staff in the development and execution of all testing methods
  • responsibility to perform sampling and/or coordination of all QC samples to any outsourced third parties
  • experience of working within a GxP highly regulated environment e.g., pharmaceutical/biotech/medical device is highly desirable as well as an understanding in the application and implementation of regulatory compliant methods in an early-stage business
  • exposure and/or experience with regulatory requirements within the QC space is a huge plus as the business continues to explore potential opportunities beyond the UK