Support review of data within the required turnaround time, including follow up and escalations as required supporting team KPIs
Prepare reports, complete review and assign comments as applicable
Operate with proficiency in job related computer applications e.g., GLIMs, Microsoft Office
Demonstrate ability to navigate, understand and comply to company test specifications and Pharmacopeia.
Maintain clear, accurate records associated with all day to day activities.
Facilitate and drive effective communication to ensure success. Liaise effectively with external groups to ensure progress of sample data review. Collaborating with others by sharing your skill set and expertise.
Support and participation in Internal Investigations
Ensure that all Quality Systems within the department are adhered to on a daily basis.
Ensure training is current for all job functions performed
Problem solving to get to root cause of issues.
Provide support with audit/inspection requirements to ensure department compliance/readiness. Participate in internal and external audits and inspections.
Qualification & Experience
‘3 - 6 years’ experience in the Pharmaceutical, Biopharmaceuticals industry.
Degree in Microbiology
Good communication, interpersonal skills and ability to work across teams.
Proven organizational skills and excellent attention to detail
Knowledge of regulatory/code requirements to EU and US pharmacopoeia
Proficiency in English, being able to speak, read and write with minimal difficulty.
Proficiency in Microsoft Office and job-related computer applications required e.g., SAP, GLIM’s