**CURRICULUM VITAE**
**MADHURIMA M**
Permanent address: Thattadathu house, Mannanam P O, Athirampuzha, Kottayam, Kerala
**PERSONNEL STATEMENT:**
Seeking to utilize my knowledge, skills and abilities to make long lasting contributions to the organization and also to gain exposure to the advanced techniques to develop my expertise while being resourceful, innovative and flexible.
**EDUCATIONAL PROFILE:**
**Qualification** | **Institution** | **% /CGPA**
—|—|—
MSc. in Microbiology (2018-2020) | Amrita School of Biotechnology, Kollam | 7.32
BSc in Microbiology (2015-2018) | St Joseph’s College, Bangalore | 6.9
12th | Sathragraha Memorial Srinarayana, Vaikom | 94.7
10th | The Warwin School, Vaikom | 8.8
**WORKSHOPS AND SEMINARS ATTENDED:**
– Attended lecture workshop on Nuclear power and methods to reduce Nuclear waste.
– Attended seminar on ‵STEM CELLS AND THEIR CLINICAL APPLICATION′ conducted by School of Regenerative Medicine and Manipal Academy of Higher education.
– Attended seminar on Mass Production of Egg Parasitoids, Trichogramma spp conducted by Dr Ganga Visalakshy at INDIAN COUNCIL OF AGRICULTURAL RESEARCH-INDIAN INSTITUTE OF HORTICULTURAL RESEARCH.
**TRAINING:**
One month at the Indo American Hospital, Chemmanakary.
**TECHNICAL SKILLS:**
**Microbiology**
– Media preparation
– IMViC test
– Isolation and characterization of microbes from various samples (food and soil)
– Spread plate and pour plate techniques, streaking methods
– Motility testing
– Staining techniques
– Kirby-Bauer method of antibiotic sensitivity testing
– Methylene blue reductase test
– Handling and culturing organisms from body fluids (blood, urine, and sputum)
– Widal test
– Production and detection of aflatoxins from fungi
– Cell counting using hemocytometer
– Immobilization of Yeast cells
– Work experience in Castor EDC, Redcap
– Knowledge of Clinical Data Management tools (CRF design, ISO standards, CDISC, CTMS)
– Knowledge of ICH-GCP guidelines
**Molecular Biology**
– Plasmid DNA isolation
– Chromatography (affinity, column)
– Techniques like PCR, agarose gel electrophoresis, SDS PAGE, Chromatography
– Competent cell preparation and transformation
– ELISA test using kit
**Soft skills**
– Team player
– Attention to detail
– Organized
– Continuous learner
**Equipment handled**
– Autoclave
– Bio photometer
– Colorimeter
– Centrifuge
– Shaker incubator
– pH meter
– Incubator
**CERTIFICATIONS:**
– Pursuing Clinical Data Management course from Biotechniqa
– Completed GWAS for Beginners from Dr. Omics lab
– Completed Fundamentals of RT-qPCR from BIO-RAD
**AREAS OF INTEREST:**
– General microbiology
– Food and Medical Microbiology
– Genetics
– Stem cell biology
**ACHIEVEMENTS:**
Received Chidambara Iyer and Lalithambal Memorial Award in higher secondary.
**PERSONNEL DETAILS:**
– Father’s name: Madhusoodhanan K T
– Mother’s name: Sudha G
– Date of birth: 16/02/1997
– Age: 28 years
– Languages known: English, Hindi, Malayalam, Tamil, Kannada
– Marital status: Married
– Nationality: Indian
**DECLARATION:**
I do hereby declare that the above particulars of information and facts stated are correct and complete to the best of my knowledge and belief.
**Skills:**
Microbiology, Media Preparation, Microbial Characterization, Molecular Biology, PCR, SDS PAGE, Clinical Data Management, Team Player, Attention to Detail
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Cover Letter:
I am writing to express my keen interest in the QA Documentation position at Rivarp Medical Pvt Ltd, Bangalore. As a postgraduate in Microbiology from Bangalore University, with hands-on training in ICH-GCP, clinical trial processes, and regulatory documentation, I am eager to begin my professional journey in the healthcare industry with a company as innovative and impactful as Rivarp.
My academic background in microbiology, coupled with specialized certification in Clinical Data Management, has equipped me with a strong foundation in quality assurance principles, regulatory compliance, and clinical documentation standards. I have also completed certified training in ICH-GCP guidelines, E6 (R2), and essential documentation processes – all of which are crucial for QA roles in regulated medical environments.
Additionally, I bring solid skills in documentation, attention to detail, and compliance, developed through academic projects and practical workshops. I am proficient in MS Office and have a strong commitment to accuracy and process integrity, which I believe are essential for ensuring high-quality documentation in clinical and medical device settings.
I am enthusiastic about the opportunity to contribute to Rivarp Medical’s commitment to patient safety and product excellence. I look forward to the opportunity to grow within your organization and am confident that my fresh perspective and dedication would be a valuable addition to your QA team.
Thank you for considering my application. I would welcome the opportunity to discuss how my qualifications align with your team’s goals in more detail.
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