www.vivobio.com Vivo Bio Tech Ltd Hyderabad : Quality Assurance Preclinical Toxicology

[muthukalee]

Head, Quality Assurance (Preclinical Toxicology)

Qualifications : M.V.Sc. (T/ Pharmacology) / M/Pharm. (Quality Assurance)

Experience : About % Years relevant experience in a Quality Assurance in a GLP-compliant Pre-Clinical Testing Facility

Job Description :
Design and Excute a Quality Assurance Program for the test facility
Preparation, review and Maintain copies of Standard Operating Procedures(SOPs)
Verify study plans for compliance with Priciples of GLP
Review study reports
Be responsible for control and issue of documents
Day-to-Day management of QA activities, including documentation
Preparedness for GLP audits by external agencieslike OECD/US FDA

About us :
Vivo Bio Tech is a full service CRO offering drug development & discovery services to pharmaceutical & biotech companies world-wide in accordance with OECD, AAALAC & IND guidelines. The company offers services in the areas of In vitro, In vivo, toxicity studies, pharmacological investigations, pharmacokinetics & toxicokinetic studies etc. Our experienced & talented scientists offer advice on defining drug development paths tailored to specific molecules. Tailored and dedicated to our clients, we distinguish your development plan is as superlative as the products you bring to our testing facilities.

Contact us :
Vivo Bio Tech Ltd.
608, 6th floor, Lingapur Complex
Himayath Nagar, Hyderabad – 500029
Andhra Pradesh, India

contact@vivobio.com
http://vivobio.com

[Guest-IJT]

Zakir Ali
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The submitted value of field named "Email :" is:
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alizakir001 AT rediffmail.com
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The submitted value of field named "Designation / Name of the Post / Skill Set" is :
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Officer Quality Assurance
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The submitted value of field named "Copy Paste Your CV / Resume Here :" is:
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OFFICER QUALITY ASSURANCE
ZAKIR MOHABAT ALI E-Mail : alizakir001 AT rediffmail.com
Objectives :
To serve best of my aptitudes in a dynamic pharmaceutical and Biotech organization which utilize my knowledge and skills.
Summary :
A result oriented professional with Three and half years experience in the field of Quality assurance in pharma industries.
Professional Qualification :
- PGDRA. (Post Graduate Diploma in Regulatory Affairs) (Appearing) From Global Institute of Regulatory affairs Pune.
- MBA. In Quality management & Material management (Appearing) From Brillient Institute of Technical Studies Meerut
- M.sc. (Biotechnology) in second division from S.R.T. University, Nanded, (M.S.)
- Bsc. (Biotechnology) in second division from Amravati university Amravati(M.S.)
Personal Skill :
- Excellent Problem solving skills, analytical ability.
- Good Verbal & written communication skill.
- Positive attitude, honesty, sincerity, hard work & quick learner.
- Strong interest to know more about new technologies.
- A dedicated and highly motivated team player with friendly nature and positive attitude.
- Easy adaptability to new methods and systems.
- Proven ability to work independently in a multicultural team environment.
Carrier Profile :
Around 3.4 years of experience in field of Quality Assurance in Pharma Industries.
Presently working with Ajanta Pharma Ltd, Paithan Aurangabad. This Plant is USFDA Approved plant, manufacturing of capsules, Tablets & having 32 loan license locations.(Manufacturing of Tablets,Capsules,Injections,Eye drops,cream,Ointment,Soap & ORS )
Designation : Officer in Quality Assurance Department Since Nov 2009 to till date
Job Responsibilities :
- Prepation,checking and Control of documents during its Distribution, Change, Review and Cancellation
o Raw material specification
o Finished product specification
o Packaging material specification
o Analytical reports
o Standard Operating Procedures
o Bill of materials
o Master formula card
o Master packing card
o Batch manufacturing Records
o Batch packing records
- Handling and investigation of market complaints.
- Handling any market returned goods received for better control to confirm the Quality.
- Investigation and control procedure for any type of deviation.
- Online quality inspection of finished products.
- Checking & Approval of artwork and maintain its records.
- Review of change control of packing material.
- Handling online rejection & control of rejected materials.
- Preparation of monthly MIS and reporting to HOD.
Previous Employer : Genom biotech Pvt. Ltd.
Designation : Officer (Quality Assurance department)
Location : Nasik
Duration : Sep 2007 to Oct 2009
Job Responsibilities :
- Responsible for co-ordination and control of all IPQA activities.
- Responsible for GMP complain on shop floor.
- Giving line clearance at different stages of manufacturing.
- Sampling and inprocess quality checks of intermediate and finish products.
- Line clearance and ensuring ISO (9000-2001), FDA, WHO environment in products.
- Responsible for validation sampling at various stages of manufacturing.
- Responsible for BMR issuing & BMR review.
- Approval of Artwork & Blockproof clearance
- Approval of shade cards & maintaining the records.
Declaration :
I hereby declare that the above written particulars are true to the best of my knowledge and belief.
Place: Aurangabad ZAKIR MOHABAT ALI
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More Information about this submission and submitter:-
___________________________________________________
Submission ID : 4108142
Date & Time : 9th May 2011 5:20 AM (UTC)
IP Address : 59.99.152.129
Browser Info : Mozilla/4.0 (compatible; MSIE 8.0; Windows NT 5.1; Trident/4.0; GTB7.0)
Predicted Country : India

[Guest]

dear sir / madam

i am herewith enclosing my cv for your kind perusal.

regards

sreevalli.