KARTHIKEYAN KESAVALU

Quality Control Specialist | Pharmaceutical Industry

A vigilant, meticulous, and erudite individual with over 4 years of pioneering experience in the
Pharmaceutical industry. Offering profound knowledge and experience in Quality Control,
Pharmacopeias,Technology Transfer, Good Manufacturing Practice (GMP), and ICH Regulations. Seeking
to prove and utilize my skills effectively and efficiently to provide impetus to my career in the process of
achieving organizational goals in the Pharmaceutical Industry.

karthikesav4296@gmail.com (+971) 547303105, (+91) 9597418109

Ras al Kamiah, United Arab Emirates linkedin.com/in/karthikeyan-k-a41535139

CAREER SYNOPSIS SKILLS

A sterling professional trajectory spanning over 4 years of
Quality Control & Management
unparalleled excellence in the sphere of Quality Assurance and
Quality Control activities in the manufacturing environment for the Corrective and Preventive Action (CAPA)
Pharmaceutical Industry.
Materials Management
Exhibited unparalleled technical prowess in testing of Raw materials,
API and intermediate for Pharma & Biotech products. Root Cause Analysis
Exemplary command of sophisticated analytical instruments which Process Validation
comply with current regulations 21CFR part 11 such as HPLC,
Dissolution tester, GC, AAS, FTIR, UV, Moisture analyzer, Testing and Troubleshooting
Refractometer, Polarimeter, Viscometer etc.
cGMP Manufacturing
Expertise in performing tests with adherence to Standard Testing
Procedures (STP), specifications, monographs, and in-house methods, GXP and ICH guidelines
ensuring accurate and reliable results.
Chromatography Techniques
Proficiency in staying updated with the latest versions of USP, EP
pharmacopoeia, ensuring comprehensive knowledge of the latest Equipment Calibration
testing requirements and standards.
Pharmacopeias Technology Transfer
Demonstrated exceptional adherence to industry-leading standards
of SOP, ALCOA principles, cGMP, GLP, GDP practices, and cutting-edge HPLC Column Evaluation
real-time reporting capabilities.
Document Management
Adept at mitigating lab incidents, OOT, and OOS with an efficient
eQMS system (Ample Logic) while collaborating with cross-functional
teams to identify and address the underlying causes.

Mastered software proficiency in Lab Solution for Shimadzu HPLC,

TECHNICAL SKILLS
Total Chrom for Perkin Elmer GC, CAMAG for HPTLC, LIMS, Ample SOFTWARE:
Logic (e-QMS), SAP, and MS Office, ensuring seamless data
LIMS, Lab solutions, CAMAG, Tiamo, Ample
management and streamlined laboratory operations.
Logic (e-QMS), SAP, MS Office.

Spectroscopy techniques:
EDUCATION Agilent Infra-red Spectroscopy: Agilent, Perkin
Elmer | Ultraviolet Spectroscopy: Shimadzu
Master of Pharmacy Chromatographic Techniques
RVS (Rathina Vel Subramaniam) College of Pharmaceutical HPTLC: CAMAG | Gas Chromatography: Agilent,
Sciences, Coimbatore | The Tamil Nadu Dr. M.G.R Medical Perkin Elmer (Lab solutions & Total chrom
University, India software) | High Performance Liquid
07/2017 - 11/2019, SGPA: 7.82
Chromatography (HPLC): Waters, Shimadzu,
Agilent (Lab solutions, Empower software)
Bachelor of Pharmacy Others:
RVS (Rathina Vel Subramaniam) College of Pharmaceutical Melting/Boiling point apparatus: Buchi |
Sciences, Coimbatore | The Tamil Nadu Dr. M.G.R Medical Dissolution | Osmometer, Polarimeter,
University, India Refractometer, Metro hm Potentiometer –
Tiamo
09/2013 - 08/2017, 68.1%

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WORK EXPERIENCE CERTIFICATES
Quality Control Specialist Registered Pharmacist by PCI | Presented
Julphar Gulf Pharmaceutical Industries by Tamilnadu Pharmacy Council of India
(TNPC), Chennai, Tamilnadu, India
01/2019 - Present, Ras Al Khaimah, United Arab Emirates Document No: 23383 A1
Achievements/Tasks
Conducting rigorous quality control tests, analyses, and inspections on raw
materials, intermediate products, and finished pharmaceutical goods, using
advanced instrumental techniques such as KF titration, infrared
spectroscopy, ultraviolet spectroscopy, chromatographic techniques, HPTLC,
DISSERTATION PRESENTED
gas chromatography, and HPLC, ensuring compliance with 21CFR Part 11
M.PHARMACY: Simultaneous
regulations.
determination of Alfuzosin
Developing and implementing robust quality control processes and Hydrochloride and Dutasteride in Tablet
procedures, employing advanced analytical techniques and state-of-the-art Dosage Form by Reverse Phase High-
equipment to maintain the highest level of product quality and ensure Performance Liquid Chromatography.
product purity, potency, and stability. (2019)
Monitoring and maintaining the calibration and performance of laboratory
equipment and instruments, ensuring accurate and reliable test results and B.PHARMACY: Estimation of Tannins in
minimizing downtime. Performing testing based on in-house specifications various parts of Cassia Fistula By
and relevant monographs (IP, BP, EP, USP), adhering to specific Titrimetric analysis and Study of its
pharmacopoeial requirements. Antifungal activity. (2017)
Collaborating closely with cross-functional teams including R&D,
Manufacturing, and Regulatory Affairs to ensure seamless coordination and
alignment of quality control activities throughout the product lifecycle.
Playing a key role in the standardization and preparation of volumetric stock PERSONAL ATTRIBUTES
solutions, solvents, reagents, and mobile phases, ensuring accurate and
consistent test results. Practicing good laboratory practices (GLP) when Impeccable Analytical skills
handling hazardous chemicals, prioritizing safety by utilizing fuming hoods,
and wearing appropriate personal protective equipment (PPE).
Empathetic & Eloquent
Conducting internal audits and inspections to assess compliance with cGMP
(Current Good Manufacturing Practices) and other relevant quality standards,
identifying areas for improvement and implementing corrective measures. Unwavering Professionalism

Investigating and resolving quality-related issues and non-conformances,

Intellectual Curiosity
employing root cause analysis techniques, and implementing corrective and
preventive actions to mitigate risks and drive continuous improvement.
Promptly reported any OOS results and effectively handled deviations, OOT
results, CAPAs, and other quality-related issues.
Compiling analytical documents, including client certificates of analysis LANGUAGES
(COA), and maintaining proper documentation and labeling of chemicals and
materials through SAP. Leading and supporting the implementation of English
quality control systems and technologies, such as Laboratory Information Full Professional Proficiency
Management Systems (LIMS) and electronic document management
systems, to enhance operational efficiency and data integrity. Tamil
Preparing and reviewing analytical equipment user requirement Full Professional Proficiency
specifications (URS), operational SOPs, training records, technical reports,
batch records, and maintaining real-time documentation during analysis Malayalam
processes. Full Professional Proficiency

Providing training and guidance to laboratory personnel on quality control

Telugu
procedures, methods, and equipment, fostering a culture of competence and
Full Professional Proficiency
adherence to best practices in quality control. Ensuring that all Quality &
Safety policies and processes are maintained at the manufacturing facility to
assure compliance with Julphar Gulf Pharmaceutical policies, procedures &
regulatory requirements.
INTERESTS
Travelling

Music

Reading

Networking

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