**Lankesh M S**
**Summary:** Lankesh M S is a skilled Research Scientist with expertise in Quality Assurance and Compliance within the GLP standards. He has experience in non-clinical study compliance, regulatory inspections, and data integrity management. Additionally, he is proficient in machine learning, bioinformatics, and toxicology.
**EXPERIENCE**
**Research Scientist (Quality Assurance – GLP Compliance)**
September 2021 – Present
Eurofins Advinus (Adgyl LifeScience Ltd)
1. Conduct study-based, facility-based, and process-based audits to ensure adherence to GLP standards (OECD, FDA, EPA, ISO 17025).
2. Review non-clinical study protocols, amendments, and reports for GLP compliance in various fields.
3. Develop and review Standard Operating Procedures (SOPs) for laboratory procedures.
4. Conduct peer reviews of raw data and reports in LIMS, Provantis, and Empower.
5. Participate in regulatory inspections, facility audits, and sponsor interactions.
6. Prepare and review Installation Qualification (IQ) and Performance Qualification (PQ) plans for laboratory equipment.
7. Ensure archival compliance and proper data retention for regulatory needs.
8. Investigate study deviations and implement CAPA strategies.
9. Assist in internal audits and Management Review Meetings to maintain ISO 17025 accreditation.
10. Maintain and review all QA records for accuracy and completeness.
11. Report inspection findings and deviations to relevant parties.
12. Provide guidance on GLP implementation and regulatory compliance.
13. Preparation of QA statements and reports for regulatory submissions.
**Lab Assistant (Forensic Analysis & Compliance)**
January 2021 – August 2021
State Forensic Laboratory
1. Ensured regulatory compliance in forensic sample handling and reporting.
2. Conducted sample receipt, chain of custody documentation, and storage management.
3. Performed forensic sample analysis and quality checks for criminal investigations.
4. Assisted in data entry and report validation.
5. Contributed to audit readiness and maintained laboratory sterility and quality control measures.
**Projects**
**Machine Learning-Based Screening of Curcuma Longa for Breast Cancer**
Duration: Six months
1. Downloaded drug dataset and performed duplicate removal.
2. Conducted SwissADME screening for pharmacokinetics.
3. Performed Exploratory Data Analysis (EDA) using Jupyter Notebook.
4. Built predictive models using Machine Learning techniques.
5. Evaluated potential bioactive compounds for breast cancer treatment.
**EDUCATION**
Msc in Zoology
Mysore
7.72
2020
**Additional Personal Info**
Address: #23/6, 3 MM Road, 1st Cross, Byatarayanapura, Bangalore – 560026
Date of Birth: 04/11/1998
Nationality: Indian
Gender: Male
**SKILLS**
GLP, Quality assurance, Quality auditing, Non-Clinical Study Compliance, Study Protocol & Report Auditing, CAPA Implementation, Regulatory Inspections, LIMS, SOP Development, Toxicology, Machine Learning, Bioinformatics.
Cover Letter:
Lankesh M S
Banglore
Date: 26-05-2025
To
The Hiring Manager
Panacea Medical Technologies Pvt. Ltd.
Malur, Kolar District
Dear Hiring Manager,
I am writing to express my interest in the Clinical Research Associate position at Panacea Medical Technologies Pvt. Ltd. With four years of dedicated experience in preclinical research, I bring a solid foundation in Good Laboratory Practices (GLP), protocol adherence, and data integrity — all essential for supporting the successful execution of clinical studies.
In my current role within a GLP-certified organization, I have worked extensively on study coordination, documentation, and compliance with regulatory requirements. My hands-on involvement with in-vitro and in-vivo studies, as well as clinical documentation and report generation, has enabled me to ensure accuracy and accountability at every stage of the research process. I have also collaborated with cross-functional teams and regulatory bodies to ensure timely submissions and audits.
What draws me to Panacea is your pioneering work in cancer therapy and medical imaging solutions. I am particularly inspired by your commitment to indigenous innovation in oncology care and would be honored to contribute to your research and development efforts.
I am confident that my experience and dedication to quality-driven research make me a strong fit for this role. I have attached my resume for your review and would welcome the opportunity to speak further about how I can contribute to your team.
Thank you for considering my application.
Sincerely,
Lankesh M S
Leave a Reply