1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
12.00 LPA TO 18.00 LPA
Position: QC Manager (Injectable)
Location: Daman
Experience: 5 - 10 YEARS
Industries: Pharma
Responsibilities:
Experience in vaccine and biological (Mabs) manufacturing,
Handled greenfield / brownfield – QC lab, qualification and validation of QC lab and instruments,
Preparation and review of all QC documents such as SOPs, protocols, reports, etc.,
USFDA and EU audit handling exposure, ...
2 Opening(s)
4.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: Production Officer (Greenfield Project)
Location: Daman
Experience: 4-5 Years
Industries: Pharma
Responsibilities:
Being a green field project, he will be part team for production department equipment’s URS and qualification documents preparation.
He will be Part of team for reviewed of technical documents for production department equipment’s.
He will ...
1 Opening(s)
8.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 12.00 LPA
Position : Assistant Manager Electrical (Project)
Location : Daman
Experience: 8- 12 Years
Industries: Pharma
Responsibilities:
Autoclaves, Medial fills
Vial washing filling sealing line
PFS filling and sealing line
Cartridge filling and sealing line
Lyophilizers and isolators
CIP SIP, visual inspection , Packing machines blister and cartoning, serialization, labelling
Manufacturing skid etc.
Above machine handling with multiple manufacturers.
I & Q of the ...
1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Asst. Manager Mechanical Engineer (Greenfield Project)
Location: Daman
Experience: 10-12 Years
Industries: Pharma
Responsibilities:
Autoclaves, Medial fills
Vial washing filling sealing line
PFS filling and sealing line
Cartridge filling and sealing line
Lyophilizes and isolators
CIP SIP, visual inspection , Packing machines blister and cartooning, serialization, labeling , Manufacturing skid etc.
Above machine ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
1.80 LPA TO 4.20 LPA
Dossier preparation as per the ACTD & CTD (Module I, II, III, IV and V) guideline.
Technical documents like Raw Material and finished products specification, manufacturing process,
Product development report, stability reports, process validations preparation & review.
Analytical method validation review as per the ICH guideline.
Drug Master File review
Technical query response to the ...