Qualification: Graduate/Post-graduate in Chemistry, Biology or Pharmaceutical Science
Experience: 3 to 5 Years in GMP/GDP operation of a Pharmaceutical company
Person should be eligible to work in UK

Job Description:

• To demonstrate expertise regarding quality assurance, Good Manufacturing Practices, and Good Distribution Practices.
• To maintain all QMS documents, preparation, control, and issue of documents.
• Handling of quality factors, Change control, Deviations, Complaints and CAPA
• Monitoring and maintaining KPIs and trends
• To write and review, when necessary, Standard Operating Procedures (SOPs)
• To communicate with CMOs, Testing Laboratories, sales, finance, and customer/suppliers for required documents and prepare ready for review and approval.
• To Coordinate with Warehouse for Testing Sample management
• Co-ordinate and compile data for Product Quality Review (PQR)
• Review of batch records and preparing for QP certification
• Participate in Internal, external and regulatory audits
• Knowledge of handling Out of specification and out of trend reports

Knowledge of handling Track wise, Trace link and SAP system will be an advantage
Job Types: Full-time, Permanent
Pay: £24,000.00-£27,000.00 per year

Benefits:

• On-site parking

Work authorisation:

• United Kingdom (required)

Work Location: In person
Expected start date: 27/09/202

Please refer the Job description for details