Lab Quality Reviewer Analyst

Job Overview

• Review and approve batch documentation in line with SOP and quality standards
• Perform lab quality review in line with SOP
• Provide services according to Production plan
• Related administrative tasks

Responsibilities

Planning and Operational Support

• Oversees work and/or serve as a lead technical expert
• Optimise and facilitate implementation of current processes
• Identify gaps in current policies and procedures
• Propose changes or improvements to processes, tools and techniques
• Provide information for reports, as required by superior
• Provide analytical support in the absence of the TL
• Provide support during regulatory audits.

Lab Quality Review

• Perform LQRs according to Production plan
• Review and approve lab records to ensure pharmaceutical analysis has been carried out as per MOA; direct queries to laboratory
• Electronic approval of analytical results on relevant software, e.g., Empower
• Evaluate and interpret chromatography data to ensure accuracy of results
• Review and approve batch documentation compliance with SOPs and quality standards
• Correct errors in batch documentation, in line with GMP standards, SOPs, and product specifications
• Record all OOS investigations and conclusions, and report to management
• Provide advice to analysts during laboratory investigations
• Provide input into SOPs
• Ensure that products are produced, tested, and stored according to the required SOPs and documentation
• Ensure adherence by Analyst/Tester before release

Reporting and Record-Keeping

• Document and store data according to SOPs and regulation
• Consolidate information for reports on a weekly/monthly basis
• Analyse consolidated data and provide recommendations
• Compile detailed and standardised reports and consolidated documents
• Initiate deviations once picked up during reviewing

Background/Experience

Skills Required

• National Diploma in Analytical Chemistry with 6+ years’ experience
• Laboratory experience

Specific Job Skills

• Understanding of pharmaceutical manufacturing and corrective action programs
• Pharmaceutical standards and compliance requirements
• Ability to interpret and implement policies, processes, and objectives
• Strong technical knowledge and be competent in the use of all laboratory equipment, software, and techniques

Competencies

• Interrogating Information
• Following Procedures
• Maintaining Accuracy
• Customer Awareness