Teja Sahithi Gottipati
Luton,UK
Summary
Accomplished professional with expertise in deviation handling and documentation, analytical skills, and process optimization. Demonstrates strong problem-solving abilities and effective communication and leadership. Adept at ensuring regulatory compliance and driving continuous improvement initiatives. Proficient in documentation review, line clearance, and compliance management. Committed to leveraging skills for organizational excellence and career advancement.
Overview
3
3
years of professional experience
5
5
years of post-secondary education
Work History
Quality Assurance Associate
Bristol Laboratories
Luton
03.2024 - 03.2025
- Provide QA support to Drug Substance and Drug Product manufacturing teams, ensuring adherence to GMP standards
- Conduct routine in-process inspections and sampling of raw materials, intermediates, and finished products
- Review quality systems, processes, and procedures for compliance with regulatory standards (FDA, ICH) and identify areas for continuous improvement
- Assist with the development and facilitation of QA training programs, ensuring effective document control and troubleshooting support
- Maintain documentation in compliance with FDA, GMP, and internal audit requirements, ensuring accurate and timely records
- Collaborate with cross-functional teams to resolve deviations, ensure product quality, and drive process improvement initiatives
- Support batch record reviews and participate in investigations for non-conformance events to ensure compliance and quality
Production Supervisor / Team Lead
Bristol Laboratories
Luton
07.2022 - 02.2024
- Supervised a team of 10+ production associates, ensuring production goals were met and GMP and safety regulations were followed
- Monitored key performance indicators (KPIs), including production yields, downtime, and defect rates, implementing corrective actions to enhance performance
- Led root cause analysis and problem-solving initiatives to address production bottlenecks, quality issues, and deviations from specifications
- Worked closely with Maintenance and Quality Control departments to ensure consistent product quality and machine reliability
- Managed daily production operations, including resource planning, scheduling, and adherence to health and safety regulations
- Ensured the accuracy of batch records, operational logs, and quality assurance documentation to maintain compliance with regulatory requirements
- Oversaw production changeovers, ensuring smooth transitions between production batches and minimizing downtime
Education
Master of Science - Project Management
BPP University
City of London 05.2021 - 04.2022
Master of Science - Pharmaceutical sciences
University of Greenwich
London 01.2020 - 01.2021
Bachelor of Science - Pharmacy
KVSR college of pharmacueticals
India 09.2013 - 03.2017
Skills
- Deviation Handling & Documentation
- Analytical Skills
- Process Optimization
- Problem-Solving
- Communication & Leadership
- Regulatory Compliance
- Continuous improvement mindset
- Documentation expertise
- Documentation review
- Line clearance
- Compliance management
Timeline
Quality Assurance Associate
Bristol Laboratories
03.2024 - 03.2025
Production Supervisor / Team Lead
Bristol Laboratories
07.2022 - 02.2024
Master of Science - Project Management
BPP University
05.2021 - 04.2022
Master of Science - Pharmaceutical sciences
University of Greenwich
01.2020 - 01.2021
Bachelor of Science - Pharmacy
KVSR college of pharmacueticals
09.2013 - 03.2017
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