| Position Title |
No of vacancies |
Qualification & Experience
|
| Manager –R&D |
1 |
M Pharma /PhD
with pharmaceutics from reputed university with 12-15 years
experience with min 5 year exp as Group Leader/Manager or
equivalent formulation in dosage form development, stability
studies. Process validation & technology transfer from
production to shop floor. Must be conversant with GMP/ cGMP
norms & related documentation. Should be well versed
with Product development for US and regulated market, NDDS.
Must be aware of the latest developments in the field. |
| Executive –R&D |
1 |
M Pharma from
a reputed university with 5-6 years experience in formulation
dosage form development, stability studies, Vendor development,
and Documentation & batch card preparation. Must be
conversant with GMP / cGMP norms & related documentation.
Exposure to ANDA regulated market development activity is
preferential. |
| Research Trainee – R&D |
2 |
Fresh M Pharma
from a reputed university with pharmaceutics as specialization
on drug development preferable tablets and capsules. |
| Asstt Manager /Sr. Executive -Regulatory
|
1 |
M Pharma with
6-7 yrs of exp in Regulatory dept. Should be Conversant
with the submissions such as ANDA, DMF, and certification
of suitability of monograph, validation protocols, Stability
protocols & SOPs development. |
| Astt Manager/ Sr. Executive -ARD
|
1 |
M Sc with 5
–6 yrs of exp in Formulation Analytical R&D dept. Knowledge
of analytical method development & validation of products
in HPLC & all sophisticated instruments. Should be well
versed with GLP and GMP aspect as per regulatory requirement.
|
| Chemist -ARD |
1 |
M.Sc (Organic)
with 1- 2 yrs of Exp in Analytical Research & Development
dept. Conversant with the development of analytical method
of formulation product, stability study of products. Calibration
and Validation of Instruments & Method development and
documentation as per cGMP and USFDA norms. |
| Manager –QC/QA |
1 |
M.Sc (Chemistry) with 12-15
yrs of Exp in QC/QA dept of a formulation unit ,out of which
min 5 years as Manager QC/QA. Well versed with all the latest
instruments, their validation, cGMP and GLP requirements.
Should be capable of leading a team. Preferential exposure
to MHRA, USFDA requirements. |
| Sr. Executive -QC |
1 |
M.Sc (Analytical Chemistry)
with 5-6rs of Exp in instrumental Analysis. Must be conversant
with calibration and validation of Instruments. Analytical
method development of new products and validation of methods.
Handling of all instruments like HPLC, UV. Spectrophotometer,
viscometer etc. |
| Microbiologist |
1 |
M.Sc (Microbiology) with
3-5 yrs of Exp in the Pharma group. Must be well versed
with microbiological analysis of RM & finished goods.
Water testing. Environmental monitoring of area and related
documentation. |
| Chemist –QC |
1 |
M.Sc (Chemistry) /B Pharma
fresh, from a reputed institute. |
| Manager -Prod |
1 |
B-Pharma with 15 yrs of exp in a Production Department of a Formulation unit preferably in oral dosage with min of 5 years as a Manager. Must be well versed with all the cGMP norms .All operational activities related to manufacturing and handling of manpower, trouble shooting at shop floor. MIS Co-ordination and documentation. Inventory control and management |
