Medicines Technician

☞ Simbec-Orion

View: 103

Update day: 01-06-2024

Location: Merthyr Wales

Category: Health / Medical Care

Industry: Research Services

Position: Entry level

Job type: Full-time

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Job content

Simbec-Orion is a responsive and agile full-service CRO, with wide therapeutic experience and specialist expertise in clinical pharmacology, oncology and rare diseases. Perfectly structured, we provide full-service clinical development solutions for small and mid-size drug developers – headed up by a centralised leadership team.With a focus on tailormade and scalable solutions, we’ll adapt our delivery style, communications and operations to suit the demands of the project, helping clients achieve their clinical and commercial objectives. Because our goal is the same as theirs; to improve patients’ lives.THE ROLEWe are looking for a Medicines Technician to join our IMP Management team where you will assist the Pharmacy Manager in managing and manufacturing products for clinical trials. The Technician will be responsible for supporting the department in activities that relate to Clinical Trial Material, such as receipt, storage, manufacture/assembly, issue, reconciliation, return or disposal to ensure projects are delivered on schedule and in accordance with Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP).Key Accountabilities
  • Maintain records of IMP, ensuring that receipt, usage, returns or destruction are logged.
  • Order, receive and check incoming goods.
  • Manufacture and dispense sterile and non-sterile IMP.
  • Prepare IMP shipments and receive returns from sites.
  • Resolve queries from Monitors/Clinical Research Associates (CRAs) during regular checks of the products and our facilities.
  • Clean and maintain IMP Management areas.
Skills RequiredESSENTIAL:
  • Minimum of 4 GCSEs (A-C) including English and Maths or overseas equivalent
  • Previous experience of working within a team
  • Previous experience of working with customers (or patients)
  • Clear verbal and written communication
  • Use of Microsoft Word and Excel
  • Able to read and carry out instructions, asking for help if required
  • High level of attention to detail
  • Ability to work to tight deadlines.
DESIRABLE:
  • Experience of working to standard procedures
  • Experience of writing standard operating procedures
  • Experience of manufacturing non-sterile and/or sterile medicines
  • Experience of working in a clean-room environment
WHY YOU SHOULD JOIN USSimbec-Orion is growing fast. To keep up with demand, we’re looking for the best people, from all areas of clinical development, to join our team.We’re dedicated to bringing the latest advances in science to market. Exposure to truly innovative new drugs in patient populations with serious unmet medical needs is what drives our company – and your reason to be a part of it.With experts from all disciplines under the same roof, you’ll work alongside some of the industry’s best. So if you’d like to further your career within challenging therapeutic areas in rare disease, oncology, or at our clinical pharmacology site, or laboratory services. We’re waiting to hear from you.
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Deadline: 16-07-2024

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