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Deeksha CV

Deeksha Srivastava is a QA professional with 7.9 years of experience in the pharmaceutical industry, currently working as a Sr. Executive at Pulse Pharmaceuticals since August 2021. She has held previous QA positions at Cian Healthcare, Mepromax Life Science, and East African India Overseas, all of which are WHO cGMP certified. Deeksha holds a B.Sc. from C.S.J.M. Kanpur University and is skilled in quality assurance processes, regulatory compliance, and documentation control.

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13 views3 pages

Deeksha CV

Deeksha Srivastava is a QA professional with 7.9 years of experience in the pharmaceutical industry, currently working as a Sr. Executive at Pulse Pharmaceuticals since August 2021. She has held previous QA positions at Cian Healthcare, Mepromax Life Science, and East African India Overseas, all of which are WHO cGMP certified. Deeksha holds a B.Sc. from C.S.J.M. Kanpur University and is skilled in quality assurance processes, regulatory compliance, and documentation control.

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divyasrivastava448
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CURRICULUM VITAE

DEEKSHA SRIVASTAVA Email id-diksha0212sri@gmail.com


Add – Awas-Vikas Colony Ram Nagar Mo.: +91-7017042398
Roorkee Haridwar.

CAREER OBJECTIVE
Looking for a challenging assignment where I can prove my ability, working knowledge solving
capability through my sincerity, dedication and my hard work that would give me an opportunity
to grow myself in the organization goal
JOB EXPERIANCE
 Currently Working with PULSE PHARMACEUTICALS PVT. LTD. Roorkee as Sr. Execu-
tive in QA Department since August 2021 to till date.
 Worked with CIAN HEALTHCARE LTD. Roorkee as Sr. officer-QA February 2019 to July
2021.
 Worked with MEPROMAX LIFE SCIENCE PVT. LTD. Dehradun as Officer-QA from
April-2018 to January 2019.
 Worked with EAST AFRICAN INDIA OVERSEAS Dehradun as Officer-QA from June-
2016 to March 2018.

 Total Experience: 7.9 Years


PROFESSIONAL QUALIFICATION
 B.Sc. from C.S.J.M. Kanpur University (2014).
 Iintermediate passed with Physics, Chemistry & Bio. From (U.P Board) in 2011 with First divi-
sion.
 High school passed with science from (U.P Board) in 2009 with Second division.

Current Job Responsibilities and Experiences


Organization – PULSE PHARMACEUTICALS PVT. LTD
Tenure - Working Since August 2021 as Sr. Executive QA.
Organization Brief- WHO cGMP certified pharmaceutical formulation plant manufacturing
Tablet, Capsule, Oral Liquid & External Preparation.
Job Responsibilities:-
1. CONTROL FUNCTION: The control function is concerned with Batch issuance, sampling,
specifications and testing, and ensure that the necessary and relevant tests are actually carried
out and that materials are not released for sale or supply, until their quality has been judged to
be satisfactory and approved.
2.TECHNICAL FUNCTION: Technical Support activities include:
1. Documentation Control (SOP’s), Prepared & Review of SOP’s
Compliance Function: This relates to Quality Assurance controls that are executed on product
Release, investigating all consumer complaints etc.
Responsible for overall co-ordination to maintain GMP and QA system in the plant.
Quality Management System:
1. Evaluation and approval of Change control, Deviation, incident and OOS.
2. Market complaint Investigate and response of Market / Customer complaint.(Ishikawa
Fishbone, 5 why analysis ,Brain storming, Fault tree analysis.)
3. Ensure REGULATORY COMPLIANCE at site.
4. To co-ordinate during the internal quality audit & external quality audits and submission of
all compliances.
5. Review, approval and implement critical quality document viz., SMF, VMP, Quality
manuals, Layouts, Protocols /Reports, SOP’s, Specification and STP. Release of finished
goods. Ensure the Self Inspection or Internal Audit of the plant
6. Coordination with FRnD, NRnD for collecting documents & review for preparation of
documents for dossier requirements to respective regulatory authority (India & Export).
Qualification & Validation:
1. Participate in Qualification & Validation
(Equipment, Water, Process) activity,
2. Preparation, Review of Qualification &
Validation Protocol & report.

Previous Company Details & Experience


1. ORGANIZATION - CIAN HEALTHCARE LIMITED
Tenure - from February 2019 to July 2021.
Organization Brief - WHO cGMP certified pharmaceutical formulation plant manufacturing
Tablet, Capsule, Oral Liquid & External Preparation
2. ORGANIZATION - MEPROMAX LIFE SCIENCE PVT. LTD
Tenure - from April-2018 to January 2019.
Organization Brief- WHO cGMP certified pharmaceutical formulation plant manufacturing
Tablet, Capsule and External Preparation.
3. ORGANIZATION - EAST AFRICAN INDIA OVERSEAS
Tenure - June 2016 to March 2018.
Organization Brief - WHO cGMP certified pharmaceutical formulation plant manufacturing
Tablet, Capsule, Oral Liquid, liquid Injection & External Preparation.

COMPUTER SKILLS
 Fundamental Knowledge of computer.
 Good basic working on Internet browsing and Internet tools.
BEING PART OF AUDITS
 Tanzania
 Uganda
 Zimbabwe
 WHO
 Sanofi
 Alkem
 Abbott
 Cipla
 Dr. Reddy
EXTRA CURRICULUM ACTIVITIES
 Participate in cultural activities during under graduate programme.
PERSONAL DETAILS
Father’s Name : Late Mr. Rakesh Kumar Srivastava
Date of Birth : May-18 1994.
Sex : Female
Marital Status : Single
Nationality : Indian
Language Known : English & Hindi
Address : Vill. Bansathi, Post- Nigoha Kanpur Nagar.
Hobbies : Travelling, Collecting knowledge.
DECLARATION

 I hereby declare that the details furnished above are true to the best of my personal knowledge
and belief.

DATE

PLACE: (DEEKSHA SRIVASTAVA)

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