LIPSALIN SAHOO

Mobile No.: 9777791761

Email: lipsalin600@gmail.com
Present Address – Manideep PG , AECS Layout , Bangalore , 560068

Carrier Synopsis OBJECTIVE

1. Micro Labs Limited Looking for an opportunity for my career growth in the field of ARD and Quality
(February 2021 – Continued) control/ Quality assurance area, where I can explore my knowledge, and personal
Total Experience – 2.2 Years growth and contribute to the development of the organization.

Currently working as
Research Associate in
Analytical R&D For Instruments handled
Regulatory Market With 1. HPLC ( Agilent and Waters)
Microlabs limited (Micro 2. Particle Size Analyser (Malvern Mastersizer – 2000 &
Advance Research Center) 3000)
Bangalore 3. Polarimeter (Rhudolph)
4. Rheometer (Anton-paar)
PERSONAL TRAITS 5. Rotary Viscometer ( Brookfield)
 Language spoken 6. USP Type-I & II Dissolution Apparatus
English, Hindi, Odia 7. UV-Vis Spectroscopy (Shimadzu)
 Adaptability 8. Vista Spectro-Photometer (HunterLab)
 Persistent
 Optimistic 9. Digital Microscope
 Hard working 10. KF Auto-titrator
 Keen observer
 Flexible

HOBIES
AREAS OF INTEREST  Recitation
 Reading story books
Analytical Research & Development, Regulatory Affairs, Quality
 Music
Assurance, Quality Control.
 Travelling
 Software Skills
1. Empower
2. LIMS
3. Lab Solution
4. Rheocalc T
5. Rheocompass
6. Easy Match
ACADEMIC QUALIFICATION
 M. Pharm (Pharmaceutical
Analysis) – (2019-2021)
(Institute of Pharmacy &
Technology, Salipur , Cuttack ,
Odisha)
 Overall Score: cgpa – 9.51
 B. Pharm – (2015-2019)
(Institute of Pharmacy &
Technology, Salipur , Cuttack ,
Odisha)
 Overall Score: cgpa – 7.85
 Council of Higher Secondary
Education, Odisha – (2013-2015)
Working area
(Gyan Bharati college of science &
technology, Bhubaneswar, Odisha)
 Percentage Obtained: 60.16
 Board of Secondary Education ,
Odisha (2013)
(Saraswati Sishu Vidya Mandir,
Paradeep)
 Percentage Obtained: 72.33
DECLARATION
I do hereby declare that all the above information given is true and correct to the
best of my knowledge and belief.
Description Of Job profile
1. Responsible for day-to-day activities of the
Development And Validation team.
2. Preparation of Development & validation/
method transfers/protocols and reports based on
R&D qualifications or monographs.
3. Supervise compliance to all cGMP or any
other regulatory requirements.
4. Ensure Development & validation Work.
5. Ensure audit trail verification in
Chromatographic and non-Chromatographic
systems.
6. Preparation of data for specification
proposals, and test methods for finished
products.
7. Initiation and ensuring the timely
implementation of changes to the existing
procedures to improve quality compliance.
1. Analytical method development and
validation .
2. Routine analysis. (Finished product, In-
process samples, stability).
3. Preparation and review of protocols and
reports for all routine activities.
4. Handling of Lab incidents & QMS
Documents.