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[QUOTE=Guest-IJT;102347]Ch.V.D.Prasad
Mobile : 09882707337,09318624999
Email : ch.prasad6 AT gmail.com

Sub: Application For a suitable post in QA.

Dear Sir/Madam,
I am a B.Sc candidate with an experience of 1+ years in Quality Assurance department. I am very much interested to pursue my carrier in your organization. I came to know from a reliable source that there exists a vacancy in QA. For your reference I am attaching a copy of my Bio-Data here. I will appreciate your calling me for an interview, so that I can explain myself better.

Thanking You,

Ch.V.D.Prasad

CURRICULUM VITAE

From

Ch V D Prasad
DNo 265/2
Shiwalik Nagar email: ch.prasad6 AT gmail.com
Jharmajri
Himachal Pradesh Ph : 09882707337

OBJECTIVE:

To dedicate the knowledge gained from experience and to work with the giants to explore the sea of Pharmaceutical sciences. To achieve the goals, which are not achieved yet.

PROFESSIONAL EXPERIENCE

Currently having 1+years of experience in Pharma industry, looking for better prospects in Quality operations.

- Currently working in M\S. zeiss pharmaceuticals pvt.ltd. , BADDI as a chemist in Quality Assurance, from april-2009 to till the date

ACADEMIC:
Bachelor of Science:

Grade – First Class from Andhra University

OTHER SKILLS:

- Trained at JKC

- Basic knowledge of Computer, MS Office, Internet

Company Profile:
Zeiss pharmaceuticals pvt.ltd is a fast growing company with dry powder injectable facility i.e. cephalosporin’s. its also does contract License production for companies like
a. Orchid healthcare ltd.
b. Lupin
c. alembic
d. Wockhardt Ltd.,India.
e. Baxter
f. Piramal healthcare
g. cipla
h. Hetero
i. Glenmark
j. Macleods

PROFFESSIONAL EXPERIENCE
INPROCESS QUALITY ASSURANCE
Principal Duties & Responsibilities.

- Implementation of QUALITY POLICY’S plan.
- Monitoring of personnel hygiene staff and workmen
- Preparation of daily reports.
- Coordination with stores, QC, Validation team and Engineering for timely implementation of production Quality.
- In processing Good Manufacturing Practices in the production area
- Preparation and review of SOP’s and formats.
- Review of batch records and GMP records.
- Preparation, review and compliance to various regulatory audits.
- Ensuring that validation schedules are implemented in time.
Dispensing
- Giving line clearance for dispensing.
- In processing of Calibration Weigh balance.
- Checking Area cleanliness, QC reference no., retest due dates, assay, and potency
- Checking RLAF calibration due dates and servicing due dates of Pre filters cleaning.
- Reviewing of GMP records daily.
- Reviewing of Approved raw materials & their retest due dates.
- Daily reviewing & monitoring refrigerated materials recording of their temperatures.
- Monitoring deferential pressure drop across the clean rooms.
Component preparation
- Monitoring the area cleanliness daily.
- Monitoring the temperatures and humidity.
- In processing the cleaning of the Equipments, Production aids, Autoclave strip charts,
- Reviewing of Equipment usage logs books, Sterilization records &GMP
Records.

Compounding preparation

- Giving line clearance for compounding preparations.
- In processing of Collection WFI.
- Collection of WFI & BET samples, sending to QC.
- Cross-Checking of Weighed raw materials before compounding.
- Maintaining & monitoring the temperatures & mixing times during compounding.
- Calibration pH meter Daily before the activity.
- Checking pH during in process of compounding.
- Collection Bulk & Bio burden samples& Sending to QC.
- Monitoring Pre & post integrity for filtrations.
Filling area
- Monitoring of particle counts, room pressures.
- Giving line clearance for washing, filling operations
- In processing the fill volumes.
- In processing online optical inspection of filled Vials,
- Monitoring the temperatures & humidity in Aseptic processing area.
- Monitoring Personnel movements of Aseptic area operators.
- Monitoring the calibration Ph meter daily before the activity.
- Reviewing of GMP records.
- Collection of Finished samples according to the sampling plan during filling sending to QC.
- Container closure integrity test.
Packaging block
- Giving line clearance for optical testing, Leak testing, labeling, overprinting, & packing of all potential formulations
- Spot checks of optically inspected vials and giving approval as per the acceptance criteria
- In processing the over printing details during labeling

- Approving, issuing & control of stereos.
- Validation of optical testing operators.
- Reviewing &closing of finished goods transfer receipt

Reporting to : Asst. Manager – QA

DOCUMENTATION CELL

Principal Duties & Responsibilities.

- Preparing Annual product quality reviews.
- Preparing & Reviewing of SOPS.
- Maintaining & reviewing & destruction of control samples.
- Receiving Market complaints & their compliance.
- Periodic reviewing of BPCR & maintaining of documentation room.
- Verification of BPR/BMR for accuracy of data & completion or record in online.
- Storage, retrieval and destruction of BPCR.
- Issuing & control of documentation records.
.
.
PERSONAL INFORMATION

Date of birth : 09-07-1988

Sex : Male

Marital status : Unmarried

Languages known: Telugu, English. & Hindi.

Permanent Address:

CH.V.D. PRASAD
S/O ADI NARAYANA
DNo- 2-111
PRATHIPADU-534146
TADEPALLI GUDEM,
ANDHRA PRADESH

Reference: Ch.V.V.Satyanarayana
Head – Quality
Zeiss Pharma Pvt. Ltd.
Ph : 09218547334

( Ch.V.D.Prasad)[/QUOTE]

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