Thilak Ramanathan
London,london
Summary
Quality compliance professional with expertise in GMP operations within pharmaceutical and healthcare sectors. Led quality management systems, deviation investigations, and CAPA initiatives while ensuring audit readiness in MHRA-regulated environments. Managed quality issues, conducted root cause analysis, and supported batch documentation review. Developed SOPs and investigation reports, utilising TrackWise and Q-Pulse for compliance and data integrity.
Overview
1
1
Certificate
8
8
years of professional experience
Work History
EMMC Scientist & Training Specialist
Virocell Biologics
02.2025 - Current
- Provide GMP QA oversight within MHRA-regulated healthcare manufacturing environments, including NHS partnerships (GOSH).
- Lead deviation investigations, CAPA implementation, and root cause analysis to resolve quality issues.
- Author and maintain SOPs, controlled documents, and compliance procedures aligned with GMP requirements.
- Support audit readiness and MHRA inspection preparation across operational processes.
- Maintain QMS records using TrackWise and Q-Pulse ensuring data integrity and regulatory compliance.
- Collaborate with cross-functional teams to ensure alignment with quality and regulatory standards.
- Support training frameworks ensuring adherence to controlled procedures and compliance expectations.
- Provide GMP QA oversight within MHRA-regulated healthcare manufacturing environments, including NHS partnerships (GOSH).
QC EMMC Scientist
Virocell Biologics
02.2023 - 02.2025
- Supported GMP compliance activities and regulatory readiness within QC operations.
- Conducted deviation investigations and CAPA implementation to resolve quality issues.
- Assisted in SOP creation, review, and controlled document management.
- Contributed to audit readiness and continuous improvement initiatives across QC processes.
QC EM Officer
Virocell Biologics
05.2022 - 02.2023
- Supported operational compliance through documentation control, training coordination, and quality tracking systems.
- Maintained controlled records and assisted in audit preparation activities.
- Contributed to GMP compliance within controlled manufacturing environments.
Lab Technician / Sterile Operator / Compliance Officer
BPL
02.2018 - 05.2022
- Supported internal and external audits ensuring inspection readiness across sterile manufacturing operations.
- Maintained GMP-compliant documentation including SOPs, training records, and operational logs.
- Documented deviations, contributed to investigations, and supported CAPA activities to ensure compliance and operational integrity.
- Coordinated training programmes and tracked compliance to enhance staff readiness and adherence to regulations.
- Supported cleanroom manufacturing processes and optimised operational workflows to maintain sterility and efficiency.
Education
BSc - Pharmaceutical Science
London Metropolitan University
London, ENG01-2014
Skills
- Cross-functional collaboration
- Controlled / Cleanroom Manufacturing Environments
- Batch oversight
- SOP management
- SOP authoring
- Training development
- CAPA ownership
- Root cause analysis
- Quality systems
- Audit readiness
- Data analysis
- Cross-functional collaboration
- Training, Compliance Support & Process Governance
- Training development
Certification
- Duke of Edinburgh Award (Bronze & Silver)
- Emergency First Aid at Work (TQUK Level 2)
- ICT Functional Skills Level 2
- University Excel Certification
Languages
Tamil
Advanced
C1
French
Upper Intermediate
B2
Interests
- Football
- swimming
- Traveling the world
Work Availability
monday
tuesday
wednesday
thursday
friday
saturday
sunday
morning
afternoon
evening
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Timeline
EMMC Scientist & Training Specialist
Virocell Biologics
02.2025 - Current
QC EMMC Scientist
Virocell Biologics
02.2023 - 02.2025
QC EM Officer
Virocell Biologics
05.2022 - 02.2023
Lab Technician / Sterile Operator / Compliance Officer
BPL
02.2018 - 05.2022
BSc - Pharmaceutical Science
London Metropolitan University
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LinkedIn: Thilak Ramanathan