Pharma Quality Assurance : Resume

[Guest]

CURRICULAM VITAE
NIJA NOBIN
Indore (M.P.)
e-mail : niganobin123 AT gmail.com

Objective :
To join a health care/ Pharmaceuticals where I can utilizes my knowledge and skills for the development of the company and where opportunities exist for the growth of my career and where I could come across the latest technology and to be a part of the team that works dynamically towards the growth of the organization.

Educational Qualification :
Sl.No Degree Board/University/Institution Year Marks Obtain
1. M.Sc. (Biochemistry) Bharathidasan University 2004-06 71%
2. B.Sc. (Biochemistry) M.G. University 2001-04 71%
3. Higher Secondary M.G. University 2000-01 58.9%
4. High School Kerala Board 1998 72%

Computer Skills & Characteristics :
Well versed knowledge of MS office and internet. Ability to learn and assimilate new information quickly, Honest and punctual.

Professional Synopsis :
- Presently working with CIPLA LIMITED, plot no. 9 &10 SEZ, Indore in Common documentation Cell (A division of Corporate Quality Assurance) as Management staff Since from September 2010 with key responsibility of documentation.

- Worked with TRAVANCORE ORGANIC BIOFERTILIZERS PVT. LTD Kottayam, Kerala in Microbiology Department as Section Officer from May 2006 to August 2009 with key responsibility of documentation.

Core Competencies :
- Preparation of Finished Product Specifications along with in process specifications.
- SOP preparation, maintenance of documents as per GMP. Review, Change and Distribution of Standard Operating Procedures (SOP’s), Specifications and Quality Formats.
- Preparation of EOPs after checking with the equipment, maintaining, issuance and retrieval of records.
- Handling of Change Control and customer approval forms for finished product specifications and communication with the customer through PRC.
- Documentation as per WHO GMP, MHRA
- To ensure Environmental conditions are maintained in respective area of the operation.
- To ensure cleanliness and sanitation of manufacturing area.
- To ensure collection of in process, intermediate and finished sample of the product being manufactured.

Special Training and Achievements :
- One month Summer Training on Techniques in Biochemistry and Biotechnology at Indian Institute of spices research, Calicut.
- Presented a Paper in the State level seminar on “Scope and Status of Photochemistry and Bioremediation at KNGA College for women Thanjavur.

Language Known : English, Hindi, Malayalam, & Tamil
Interest and Hobbies : Traveling, Music, Cooking.
Key Strengths : Hardworking and sincere with good communication skills and an ability to do whatever determined.

Personal Details :
Nationality : Indian
Age : 26
Date of Birth : 12th Aug. 1983
Marital Status : Married

Declaration
I hereby declare that above mentioned details are correct and complete to the best of my knowledge
Date :
Place : Indore (Nija Nobin)

[Guest]

RESUME

Name : CH.RENUKA
Email :cherukurenuka AT gmail.com

Career Objective
To be associated with a progressive organization that gives scope to apply my knowledge and skills, and to be part of team that dynamically works towards the growth of organization.

Education (Specialization) College , University Year of Education Percentage
B. Pharmacy R.B.V.R.R Women college of pharmacy 2009- 2012 65%
D. pharmacy K.L.R Pharmacy college 2007-2009 80%
Intermediate Narayana junior college 2005-2007 83%
S.S.C Pragathi high school 1995-2005 76%

Technical Skills :
Operating System :Window 98, XP
Language : C language

Handling of uv-spectrophotometer .all analytical equipments in pharmacy manufacturing of tables,capsules and all pharmaceutical products.Efficient skill in laboratory work.

STRENGTHS :
Positive thinking, self-confidence, possessing leadership qualities, interest in learning.

INTERESTS :
Quality Control and Evaluation of Dosage form

Personal Details :
Name : CH. Renuka
Father’s Name : CH.Venkateshwarlu
Date of Birth : 07-05-1990
Hobbies : playing shuttle, listening to music
Permanent Address : kothagudem, khammam

I hereby declare that the above written particulars are true to the best of my knowledge and belief

Place : Hyderabad Signature

[Guest]

B. N.M.MANOHAR
E-Mail : madhubalishetty AT gmail.com

OBJECTIVE :
To work as a task oriented/Quality specialist in a highly regulated, ever-changing Pharmaceutical industry where in I can put all my acquired skills and abilities to the optimum use to bring out the best for the company and myself.

EDUCATIONAL QUALIFICATION :
M.Sc Bio chemistry from National P.G. college, Nandyal in the year 2010-2011 with an average of 60%.
B.Sc. Bio technology, Bio chemistry & Chemistry from Sri Ramakrishna Degree Autonomous college, Nandyal in the year 2006-2008 with an average of 60%.
Intermediate from the Board of Intermediate Education, A.P.
S.S.C from Board of Secondary Education, A.P

Computer Skills : Computer Applications – Experience with MS Office, Internet, C etc…

PROFESSIONAL EXPERIENCE : (1Y)
Orem Access Bio. Inc., Hyderabad,
Designation : Executive-QA
AREA OF INTERST :Quality Assurance,Research and Developement

HIGHLIGHTS OF EXPERIENCE :
- Exposure in all aspects of Pharma QA – Documentation
- Exposure in all Raw material and Packing material inspections.
- Exposure in maintenance of controlled samples and their records.

KEY RESPONSIBILITIES :
- Control of Documents :
Control of all master documents and obsolete documents like
1. Standard Operating Procedure, Operating Instructions, Cleaning Procedure, Guidelines.
2. Packing Material, Intermediates, Finished Product, Stability Specification/ Test Procedure & General Test Procedures.
3. Validation Protocols and their Status. Site Master File, Validation Master File & Quality Manual.

- Distribution & Retrieval of Documents :
1. All the approved documents – user copies distribution as per the SOP and retrieval of obsolete documents promptly.
2. Maintaining Issue Records for all controlled documents.

- Issue, Retrieval & Archival of Documents :
1. Issue of Batch Manufacturing records, Batch Traceability Records, Batch Packing Records, Record of Analysis, Registers, Usage Log Books, etc..., retrieval of the same after execution and archive till their retention period as per SOP.
2. Archiving documents systematically for easy retrieval.

- Co-ordination to Change Controls :
- Promptly following for implementing, documents revision, approval, training, effective & disposal of change controls.
- Support for Incidents, Deviations, and Market complaints.
- Good exposure in close the Customer/Market complaints.
- Create the Complaint forms and investigation Report Records.
- Review of SOPs, Guidelines, and Formats etc…
- Preparation of all master lists and updating as on date.
- Co-ordination to in plant and on the job trainings.
- Good exposure in MS Word, Excel presentations.
- Arranging documentation support to Internal and Regulatory Audits.

- Raw Material and Packing Material inspections :
- Raw material and Packing Material tested as per the given supplier COA.
- Good exposure in Online inspections of manufacturing products.
- To given the COA’s and Test Reports and labels of finished products to concern departments.

- Maintain control samples and Records :
- To maintain the control samples and control samples records as per related SOP.

DECLARATION :
I here by declare that the information furnished above is true to best of my knowledge.
Place : Hyderabad
Date : 05.01.2013
(Manohar.B)