Senior QA Associate

MeiraGTx; Greater London; Ibrido; GBP 65.000 - 95.000; Tempo pieno

Descrizione del lavoro

MeiraGTx in London is seeking an experienced QA professional to provide oversight to manufacturing operations and support functions, ensuring GMP compliance and timely product release. You will lead the QA team, manage the Quality Management System, review GMP documentation, and drive continuous improvement and training across operations.

This role requires 5+ years in sterile GMP environments, strong regulatory knowledge, and proficiency with Microsoft Office and eQMS systems.

Competenze

• Minimum 5 years’ experience in a sterile GMP manufacturing environment.
• Excellent understanding of Quality Management Systems.
• Strong knowledge of Regulatory inspections and client audits.
• Proficient in Microsoft Office and experience in database use and eQMS systems.
• Data gathering, analysis and structured thinking to support decisions.

Mansioni

• Provide QA oversight to manufacturing operations and supporting functions.
• Manage the Quality Management System and GMP documentation.
• Review batch documentation and ensure timely GMP-compliant release.
• Lead internal audits, inspections and CAPA processes.
• Support continuous improvement of the Quality Management System.
• Coordinate CAPAs, deviations, change controls and OOS investigations.

Conoscenze

Quality Management Systems

GMP manufacturing

Regulatory inspections

Microsoft Office

eQMS systems

Data analysis

Stakeholder management

Strumenti

Microsoft Office

eQMS systems

Descrizione del lavoro

Your mission

• Provide experienced QA support and oversight to MeiraGTx operations.
• Ensure QA regulatory compliance and product quality requirements are met at all times, as well as facilitating product release in a timely manner.
• Coach and train the QA team and other functions and continuously improve the local Quality system and provide training & support for Quality relevant systems.

Job Description

Major Activities and Responsibilities:

• Provide QA oversight to the manufacturing operation and supporting functions.
• Management of the MeiraGTx Quality Management System.
• Generation, Review and approval of relevant GMP documentation.
• Create and Review QA Processes. Create/review Standard Operating Procedures, Policies and Training material.
• Maintain QA KPI metrics.
• Collaborate with Operational areas, supporting the Team Lead to manage the day-to-day QA Operations.
• Review Batch documentation and support QA team review of Batch documentation. Ensuring timely and adequate release of GMP compliant product in accordance with Regulatory and site-specific authorisations.
• Manage and support QA team Facility Walk rounds and QA support for all operational areas.
• Provide direct quality team support during customer and regulatory audits.
• Perform internal audits and inspections and audit write up.
• Quality Systems: Complete Reporting, reviewing, investigating, root cause analysis, assessing Quality Risk Assessments, Incidents, Deviations, CAPA’s, OOS, Change Controls and temperature excursions.
• Support Document Management activities when required.
• Proactively initiate and support continuous improvement of the Quality Management System.
• Deliver compliance training to operational areas.
• Provide guidance and assistance to quality related issues in Operational areas and to External third parties.
• Deputise for the QA Team Leader – Operations when required.
• Proactive individual, able to step in without being asked. Identifies upcoming activities or tasks and works on completion without the need to be asked.
• Collaboration and stakeholder management.
• Adaptability ad resilience.
• Supports innovation by challenging outdated practices and encouraging better ways of working.
• Always asks and understands the “why” and is capable of explaining this to others. Does not automatically accept the status quo.
• Finds better ways for completing existing activities/processes saving time or effort while remaining compliant.
• Data driven decision making. Able to check reliability of sources, identify gaps, inconsistencies or misleading information.
• Demonstrates critical thinking and logical reasoning.
  

Key Job Competencies and Behaviours

• Minimum 5 years experience of working within a sterile GMP manufacturing environment.
• Excellent understanding of Quality Management Systems.
• Demonstrate very good understanding of the purpose of the regulation requirements in terms of how they translate to product quality and patient safety.
• Proficient in Microsoft Office and experience in database use and eQMS systems.
• Excellent interpersonal skills. Role model for professional behaviours, respectful relationships, positive and constructive communication.
• Capable of demonstrating structured thinking, data gathering and analysis for informed decisions.
• Good organisational and time management skills and able to demonstrate flexibility and adaptability. Capable of consistent on-time delivery of their individual tasks and responsibilities. Able to prioritise workload, decisive thinker able to work within agreed timescales.
• A high level of attention to detail.
• Good team player and must also be able to workindependently.
• Strong experience in Regulatory inspections and Client audits.

Job Background

• Experience working in a Sterile manufacturing GMP environment including a minimum 5 years’ experience in Compliance and Quality Assurance.
• IT literate, experience managing and operating an electronic QMS.
• Excellent verbal and written communication skills.

Why us?