The Central Drugs Standard Control Organization (HQ), FDA Bhawan, Kotla road, Near
Mata Sundari College, New Delhi - 02 requires Professional Consultant, Technical Data Associates, Data Entry Operators and Office Assistants purely on contractual basis upto 30.09.2011. These supporting staff will assist Senior Officers in matters related to Administrative/ Technical works carried out in the office of CDSCO. Qualification, experience, job description, emoluments etc. for various posts are as under:-
1)Professional Consultants
a) Professional Consultant Medical Devices @ Rs. 50,000/- p.m
Age: 35 - 65 years
Qualification:
(i) Master degree in Chemistry / Pharmacy/Biochemistry or Degree in Bio-Medical
Engineering with 10* years experience in Manufacture/Testing/ Research/Regulatory affairs
of Medical Devices.
Job Description:-
1. To collate, compile and analyse the scientific national, international data/regulation of
medical devices.
2. To make relevant SOP’s, guidelines and notification for amendments in Schedule M-III
and M-IV to Drugs & Cosmetics Rules.
3. Any other duties assigned by Drugs Controller General of India (DCGI) from time to time
(b). Professional Consultant Diagnostic Kit @ Rs. 50,000/- p.m
Age: 35 - 65 years
Qualification:
(i) Master degree in Pharmacy/ Medical Lab Technology/ Biochemistry/ Microbiology or
degree in Bio-Medical Engineering with 10* years experience in Manufactures/ Testing/
Research /Regulatory affairs of Diagnostic kits.
Job Description:-
1. To collate, compile and analyse the scientific national, international data/regulation of
Diagnostic kits.
2. To make relevant SOP’s, guidelines and notification for amendments in Schedule M-III
and M-IV to Drugs & Cosmetics Rules.
3. Any other duties assigned by Drugs Controller General of India (DCGI) from time to time
(c) Professional Consultant Pharmacovigilance (Tech.) @ Rs. 50,000/- p.m
Age: 35 - 65 years
Qualification:
Master degree in Pharmacy with pharmacology or clinical pharmacy with 10* years
experience in collation/ analysis of ADR reports.
Job description:-
To prepare the blueprint for collection, Collation, analysis of ADR reports, received
from various centres all over the country and implementation of the Pharmacovigilance
programme. Preparation of guidelines / documentation etc. for the programme. Co-ordination
of spurious drugs survey at National Level. Any other duties assigned by Drugs Controller
General of India (DCGI) from time to time
(d) Professional Consultant Biopharmaceuticals @ Rs. 50,000/- p.m
Age: 35 - 65 years
Qualification:
Master Degree in Pharmacy with Pharmacology or clinical Pharmacy or M.Sc. in Clinical
Chemistry with 10* years experience in manufacturing/testing/Regulatory Affairs of
Biopharmaceuticals
Job description:-
- To prepare guideline documents for conducting Clinical Trials, manufacturing and
testing of Biopharmaceuticals
-To facilitate the preparation of guideline document for approval of New
Drugs(Biopharmaceuticals) and for CRO centers.
-Any other duties assigned by DCG(I) from time to time.
(e.) Professional Consultant Clinical Trial @ Rs. 50,000/- p.m
Age: 35 - 65 years
Qualification:-
Master degree in Pharmacy with pharmacology or clinical pharmacy with 10* years
experience in co-ordination/ documentation/ management of Clinical Trial.
Job description:-
1. To facilitate the preparation of SOP’s, guidelines, roadmap for
registration of CROs, Ethics Committees; inspection of Clinical Trial sites, sponsors
/CROs ; GCP training etc
2. To facilitate the preparation of guidance document for approval of various categories
of new drugs , clinical trials including micro dosing (phase zero) and phase –I clinical
trials.
3. Any other duties assigned by Drugs Controller General of India (DCGI) from time to
time
(f).Professional Consultant Cosmetics @ Rs. 50,000/- p.m
Age: 35 - 65 years
Qualification:-
Master degree in Pharmacy with 10* years experience in manufacturing/ testing of cosmetics.
Job description:-
1. To prepare the SOP’s, Guidelines on regulation of import of cosmetics.
2. To maintain Documentation & Data-base
3. Any other duties assigned by Drugs Controller General of India (DCGI) from time to
time
(g). Professional Consultant IT Services @ Rs. 50,000/- p.m
Age: 35 - 65 years
Qualification:-
1. B-Tech /B.E (computer science) or MCA
2. 5 years experience in management/ development of software in a reputed organization.
Job description:-
1. To facilitate E- governance project.
2. To train the staff to implement E- Governance and File Tracking System.
3. Development of electronic Archiving and retrieval system.
4. To maintain Documentation & National Data Bank.
5. Upgradation of website and its up keep.
6. Installation of Video conferencing facilities with wi-fi system.
7. Preparation of user manual etc.
8. Any other duties assigned by Drugs Controller General of India (DCGI) from time to time
(h). Professional Consultant Quality Management System @ Rs. 50,000/- p.m
Age: 35 - 65 years
Qualification:
Master degree in Pharmacy with 10* years experience in quality management in
Pharmaceutical field.
Job description:-
1. To facilitate implementation of quality management system and its monitoring.
2. Training of staff
3. Harmonization with national/ international QMS progress.
4. To prepare and maintain documentation
5. Preparation of guidelines/ operating documents for the organization.
6. Any other duties assigned by Drugs Controller General of India (DCGI) from time to time
* 10 years experience may be relaxed for highly skilled and qualified candidates.
2. Technical Data Associate (22 Posts) @ Rs. 19,000/- p.m
Qualification:-
The candidates should be B. Pharmacy or M.Sc. in Biochemistry, Pharmaceutical
Chemistry/Organic Chemistry/Microbiology/ Biotechnology. The candidates should
also have sound knowledge of computer operation. Preference will be given
candidates having experience in manufacturing/ testing of drugs/drugs regulatory
affairs.
Job description:-
To assist officers of CDSCO in scrutiny/examination of technical documents
pertaining to import registration, Import license, new drug approval, Central Licence
Approving Authority (CLAA) items and various NOCs. Documentation, Creation and
maintenance of National Data Bank. Any other duties assigned by Drugs Controller
General of India (DCGI) from time to time.
government servant having experience in the field of administration and finance.
3. Data Entry Operator ( 18 Posts) @ Rs.10,000/-p.m.
Qualification:
The Candidates should be Graduate with 1 year Diploma in computers from recognized
Institute. The candidates should have typing speed of 40 w.p.m. Preference will be given to
candidates also having short hand knowledge.
Job description:-
Typing of various letters, approvals, licenses, noting etc. Alongwith documentation, Creation
& maintenance of National Data Bank. Any other duties assigned by Drugs Controller
General of India (DCGI) from time to time.
