SHIVAPAVANI DHARAVATH
Ongar,Ireland
Summary
Motivated Manufacturing and Quality professional with experience supporting GMP-regulated pharmaceutical and medical device environments. Strong exposure to manufacturing operations, packaging processes, validation support, and technical documentation, with hands-on experience in process improvement, root cause investigations, and Right First Time delivery. Currently completing an MSc in Medical Devices Technology & Business, with a strong interest in Advanced Manufacturing Engineering, Packaging Engineering, and New Product Introduction (NPI). A proactive team player with strong communication skills and a drive for high-quality, on-time project delivery.
Overview
6
6
years of professional experience
2
2
years of post-secondary education
Work history
Quality & Operations Support Associate
Bidvest Noonan – Client Site (Regulated Manufacturing Environment)
Dublin
01.2025 - 02.2026
- Support operations within highly regulated environment, ensuring adherence to procedures, safety, and quality requirements.
- Prepare and maintain incident reports, deviation-related documentation, and technical records in line with quality system expectations.
- Work closely with engineering, operations, and site management teams to gather accurate inputs for investigations and corrective actions.
- Support equipment performance monitoring, issue escalation, and follow-up actions to maintain operational efficiency.
- Maintain high standards of documentation accuracy, data integrity, and inspection readiness.
Quality Control Analyst (cGMP Environment)
CSIR – Indian Institute of Chemical Technology (IICT)
Hyderabad, India
10.2021 - 08.2024
- Supported manufacturing and process development activities through generation and review of GMP-compliant technical documentation.
- Performed analytical testing to support process qualification, validation batches, and stability studies.
- Contributed to root cause investigations for analytical and process-related issues and supported implementation of corrective actions.
- Collaborated cross-functionally with Manufacturing, Engineering, QA, and Validation teams.
- Supported continuous improvement initiatives focused on efficiency, Right First Time documentation, and compliance.
- Operated and supported HPLC, GC, Empower, and Open Lab systems, ensuring equipment performance and data reliability.
Industrial Trainee – Quality Control & Validation Support
Rainbow Pharma Lab
Hyderabad, India
08.2020 - 10.2021
- Supported equipment qualification and cleaning validation activities.
- Assisted in preparation and review of validation documentation (IQ, OQ, PQ exposure).
- Gained foundational experience in GMP documentation, SOPs, and regulated laboratory practices.
Production Operator – Manufacturing & Packaging Operations
Amogen Pharma Pvt. Ltd.
01.2020 - 08.2020
- Operated manufacturing and packaging equipment in compliance with SOPs and GMP requirements.
- Supported packaging processes, material handling, and equipment operation to achieve daily production targets.
- Executed and documented in-process quality checks, ensuring traceability and product performance.
- Identified process issues and supported technical investigations and corrective actions.
- Contributed to lean manufacturing initiatives and supported continuous improvement efforts.
Education
MSc - Medical Devices Technology & Business (QQI Level 9)
Innopharma Education, Griffith College
Dublin 09.2024 - 10.2026
Skills
- Advanced Manufacturing & Operations Support
- Packaging & Labelling Process Support
- New Product Introduction (NPI) Support
- Process Verification & Validation (IQ, OQ, PQ – support)
- GMP & Quality System Compliance
- Manufacturing Documentation (MP, IP, BOM)
- Root Cause Analysis & Corrective Actions
- Lean Manufacturing & Continuous Improvement
- Cross-Functional Collaboration
- Technical & Regulatory Documentation
- GMP & Quality Management Systems
- Manufacturing & Packaging Documentation
- Validation Documentation (IQ, OQ, PQ – support)
- Root Cause Analysis (5 Whys, Fishbone)
- Microsoft Word, Excel, PowerPoint
- HPLC, GC, Empower, Open Lab
- Lean / Continuous Improvement Principles
PERSONAL ATTRIBUTES
- Strong written and verbal communication
- Energetic, self-driven, and results-focused
- Well organized with excellent attention to detail
- Effective team player in cross-functional environments
- Able to work independently with general supervision
Timeline
Quality & Operations Support Associate
Bidvest Noonan – Client Site (Regulated Manufacturing Environment)
01.2025 - 02.2026
MSc - Medical Devices Technology & Business (QQI Level 9)
Innopharma Education, Griffith College
09.2024 - 10.2026
Quality Control Analyst (cGMP Environment)
CSIR – Indian Institute of Chemical Technology (IICT)
10.2021 - 08.2024
Industrial Trainee – Quality Control & Validation Support
Rainbow Pharma Lab
08.2020 - 10.2021
Production Operator – Manufacturing & Packaging Operations
Amogen Pharma Pvt. Ltd.
01.2020 - 08.2020