Working under limited supervision to package Clinical Trial Supplies and Commercial pharmaceutical products, to cGMP standards and procedures. * To comply with company policies including internal and external Health and Safety and Environmental standard's as required. * To work in a safe manner with due regard to […]
* Responsible for ensuring that all project deliverables meet client agreed milestones and that support functions are aligned to deliver on time if full under excellent client service * To forecast and report accurate financial performance of client accounts whilst driving organic growth of repeat business through […]
* To ensure the effective administration, monitoring and completion of Quality System activities at PCI Tredegar. * The job holder is required to work on their own initiative and largely independently on key responsibilities under the supervision of the Senior Quality Specialist. * The job holder is […]
Job Description: Job Title: QA Document Administrator Location: Bridgend Department: Quality Assurance (QA) Work Pattern: 40 hours per week Reporting to: Senior QA Officer Responsible for (staff): N/A As a QA Document Administrator you will maintain controlled documentation within the company’s electronic document management system and provide general administrative support to the QA Department. Essential […]
When it comes to pharmaceutical and biopharmaceutical supply chain expertise who do you trust?
Your bridge between life-changing therapies and patients