A reputed pharmaceutical company engaged in development, manufacturing and marketing of oral solid dosages forms in regulated market. We are looking for competent growth oriented candidates for our USFDA & Eu-GMP approved OSD manufacturing facility at N-32, Additional Patalganga MJLDC, Tal.- Panvel, Dist.- Raigad.
Production
Section : BQS - Primary/Secondary Granulation Bottling packing - Primary/ Secondary
Post : Operators
Qualification : Any Graduate Under graduate Any Diploma / ITI
Experience : 02-05 Year
Desired profile : • Handling of production machines such as BQS, Coating, Granulation. Bottle line packing machine primary and secondary.
• Record and maintain proper documentation of Production area.
Quality Control / Analytical Lab
Section : Raw Material / Stability Studies/ FP/IP/ GLP / QMS / AMV
Post : Officer / Executive
Qualification : M.Sc./B. Pharm/ M.Pharm
Experience : 02-05 Year
Desired profile : • Should have experience in analysis of RM. PM. FP, IP. Stability.
• To operate sophisticated instruments like HPLC. GC, UV. FTIR, Dissolution Etc.
• Record and maintain proper documentation.
Quality Assurance
Section : ALQA/Finished' Stability/ Method Validation/ Lab QA/ GLP Document Control
Post : Officer / Executive
Qualification : M.Sc. / B. Pharm / M. Pharm
Experience : 02-05 Year
Desired profile : • To review protocols of method validation/verification, stability protocol, calibration, qualification document.
• To review raw material and packaging material specification/MOA.
• To review the stability and finished product data like calculation sheets, COA and summary' report. Hands on experience in Quality Control testing of release and stability sample of finished product, review the electronic data, audit trail, integrations.
Quality Assurance
Section : QMS Section
Post : Officer/ Executive
Qualification : B.Pharm / M.Pharm
Experience : 02-05 Year
Desired profile : • Coordination and evaluation of QMS (Change control. Deviation, CAPA)
• Training Management- Approval of training, allocation of training followed by tracking.
• New product initiation and evaluation/tracking
• Preparation and review of sectional and cross functional department SOP’s.
• To carry out all responsibilities assigned by section head as per cGMP. GDP and zero data integrity.
Walk in Interview
Date : 13th Jan 2026, Day :- Tuesday
Time : 02:00 pm to 05:00 pm
Venue : N-32, Additional Patalganga MIDC, Village karadc Budruk. Tal.- Panvel, Dist.- Raigad
See All Ph.D Alerts M.Pharm Alerts B.Pharm Alerts Maharashtra Alerts
See All Other Jobs in our Database
Subscribe to Pharmatutor Job Alerts by Email
