QP Contract

Location
Switzerland
Salary
Dependant Upon Experience
Posted
04 Jun 2021
Closes
04 Jul 2021
Hours
Full Time
Contract Type
Permanent
Experience Level
Management
  • Main duties would be to ensure that all Quality and Compliance requirements are met for Customers, Suppliers, Internal Departments and Regulating Agencies in accordance with applicable EU regulations.
  • Management of various quality parameters, such as; Complaints, Deviations & CAPA, Audits, Quality Metrics, SOPs, Change control, Specifications, Manufacturing Documentation Approval and Training and Batch Certifications.
  • To provide QP GMP declarations including on site audits if required.
  • Review study and lot specific documentation necessary to facilitate QP Release. Use technical knowledge to assess the criticality of any issues.
  • Liaising with the Regulatory Authorities.
  • Provide support for resolution of technical problems involving existing global supply products
  • Actively encourage input/development of QMS, Site Quality/EHS Councils and Continuous process improvement.
  • Experience in auditing suppliers, consultants, API facilities, and drug product manufacturing or testing sites.
  • Should be eligible Qualified Person with experience in undertaking the routine duties of a Qualified Person and in a Quality related role within the pharmaceutical industry.Background and skills
  • Relevant University Qualification in the chosen area of expertise
  • Minimum of 2 years pharmaceutical experience or associated manufacturing industry experience.
  • Knowledge in sterile, solid and liquid dosage forms.
  • Broad knowledge of pharmaceutical manufacturing processes.
  • Good inter-personal skills and presentation skills.
  • Location: UK or Europe
  • Fluent in English or any other European languages