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Damaragidda Raghavendar

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43 views4 pages

Damaragidda Raghavendar

Uploaded by

Naveen
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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CURRICULUMVITAE

Raghavendar. D
S/O D. Balraj
H.No: 15-5-42/1,
Koil Konda “X” Cross Roads,
TD Gutta, Mahaboob nagar-509001.
Email: [email protected]
Mobile: +91- 9494268454

CAREER OBJECTIVE:

A career in a team driven organization where I can use my scientific expertise and knowledge in best
possible way for the growth and development of organization as well as my own improvement.

PERSONALITY:

Highly motivated with professional attitude and work ethics. Work well independently and as apart
of a team. Friendly, reliable, very well organized creative self-starter and eagerness to learn newer

PROFESSIONAL EXPERIENCE:
technologies.

 Currently working as a Senior Executive in ASPIRO Pharma Limited (As a Group of


Hetero), from Sep-2023 to till date.

Formulation Analytical Research & Development:


 Analytical Method Development Report (MDR), Tentative Method of Analysis (Tentative MOA).

 MVP (Method Validation Protocol) with Annexures, MVR (Method validation Report),
Specification & STP (Standard Test procedure), Method Equivalency protocol & Report, Method
Transfer protocol & Report.

 Technology Transfer (T.T) sent to Site Transfer.

 Worked as a Senior Executive in Etico Lifesciences Pvt. Ltd. From Mar-2022 to Sep-2023.

PREVIOUS EXPERIENCE:
 Working in Review (QA Operations) team for review of the following documents
Formulation Research Development:
1. Product Development Report (PDR), QTPP (Quality Target Product Profile).
2. Stability study protocols and Report reviews, loading and unloading of stability samples.
3. MFR or BFR (Master formula record or Batch formula record), BPR (Batch packaging record).
4. Qualitative & Quantitative composition Report (QQR).
5. Process, Formula Optimization protocol & Report, Pre formulation protocol & Report.
6. Technology Transfer Protocol & Report (TT protocol & Report).
7. Preparation of Internal Audits schedules, vendor Audits, calibration Schedules & Trainings.
8. Responsible for installation of Equipment/Instrument Qualifications. Issuance and retrieval of
documents.

 Biophore India Pharmaceuticals Pvt Ltd as a Executive in DQA (Formulation Development


Quality Assurance) department, from Oct-2018 to Feb-2022.

Formulation Analytical Research & Development:


 Analytical Method Development Report (MDR), Tentative Method of Analysis (Tentative
MOA).

 MVP (Method Validation Protocol) with Annexures, MVR (Method validation Report),
Specification & STP (Standard Test procedure), Method Equivalency protocol & Report,
Method Transfer protocol & Report.

 Technology Transfer (T.T) sent to Site Transfer.

Formulation Research & Development:

 Product Development Report (PDR), QTPP (Quality Target Product Profile), Vendor
Qualifications.

 Bench Scale Development Report (BDR), BMR or BPR (Batch manufacturing record or
Batch processing record).

 MFR or BFR (Master formulae record or Batch formulae record), BPR (Batch packaging
record).

 Dissolution Equivalence Report, Qualitative & Quantitative composition Report (QQR).

 Process, Formula Optimization protocol & Report, Pre-formulation protocol & Report,
Execution of Bio-batch and Scale-up Batch Execution/Batch execution.
 Technology Transfer Protocol & Report (TT protocol & Report).

 Preparation of External Agreements, Internal Audits schedules, vendor Audits, calibration


schedules & Trainings.

 Responsible for installation of Equipment/Instrument Qualifications.

 Issuance and retrieval of documents.


 Worked as an Chemist in Pellsys Pharma Pvt Ltd in QA department from Jan2016 to
Sep 2018.

 Issuance, distribution, archival and retrieval of documents.

 Review of BMR and BPR, Production activities.

 Review& preparation of Annual Product Quality Review (APR’s/ APQR’s).

 Responsible for installation of Equipment/Instrument Qualifications.

 Responsible for Line clearance activities like dispensing activity, raw materials & packing
materials.

 Responsible for Yield calculations and Assay Calculation at dispensing stage and ensuring
that the materials are dispensed as per the standard quantities mentioned in the BMR &
BPR.

 Responsible for performing in-process checks during manufacturing operation like


granulation, compression, coating and inspection as per respective BMR.

 Sampling in different stages of manufacturing process and complete batch monitoring.

 Responsible for Sampling of the rinse & swab sample.


EDUCATIONALPROFILE
M.PHARMACY (2017) – Sri Indu Institute of Pharmacy, Hyderabad – JNTUH - 75%.

B.PHARMACY (2015) –Teegala Krishna Reddy College of Pharmacy, Hyderabad –JNTUH - 54%.

INTERMEDIATE (2009)-Takshashila Jr college, Mahabub nagar -52%.

SSC (2007)–ZPHS Boys High School, Mohammadabad- 57%.

ACHIEVEMENTS

 Participated in several co-curricular activities in school.


DECLAREATION:

I hereby solemnly declare that all the information provided here is true to the best of my knowledge.
If given the chance, I assure you that I will prove myself to be a worthy asset of your organization.

Place : Yours faithfully


Date : (D. Raghavendar)

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