RS 1,25,000 To 3,25,000 Baddi, Mohali ( Chandigarh )
qc - Handling of Instruments like Hplc, Analysis of Finished Product, Raw Material and in Process Samples as per Standard Testing Procedure and Pharmacopoeial Reference, Analytical Chemist, Testing
preference: Male Candidates
Designations - QA / QC And Production Executive.
Required Education - B Pharma / M Pharma / BSc / MSc Freshers and experience Holders.
Preference - Only Male Applicants can Apply.
Industry / Company - Pharmaceuticals.
No. of Openings - 20 Plus.
RS 1,00,000 To 3,00,000 Baddi, Mohali ( Chandigarh )
To Ensure and maintain the work discipline on shop floor.
Prepration of daily compression, coating, inspection and packing plan
To ensure all CGMP requirements for compression, coating, Inspection and packing activity.
To ensure that products are ...
Key Skills : production officer,production planning,production,inspection,production controller,production...
Ensure stringent Quality standards, norms & practices and effective deployment of GMP.
- Develop & implement all manufacturing business systems covering all the functions.
- Build and lead teams to achieve business goals.
- Ensure OTIP man...
RS 1,25,000 To 1,75,000 Baddi, Mohali ( Chandigarh )
Candidates should have experience in:-
1. GLP activities of QC lab, Maintenance, Calibration & operation of all Laboratory equipment & instruments
2. Management of reference standards/working standard/Qualification of instruments
3. Sampling of Pa...
Key Skills : lab assistant,quality control incharge,quality analyst,lab incharge,quality...
RS 1,25,000 To 3,75,000 Baddi, Mohali ( Chandigarh )
-Analysis of raw material chemical method and instrumental method.
-Preparation of Volumetric reagents and solutions.
-Analysis of in process and finished product (Capsules & Tablets).
-Sampling and inspection of Received Raw & Packing Mater...
RS 1,50,000 To 3,25,000 Baddi, Mohali ( Chandigarh )
We are looking for a male candidate who is having experience in managing QA and QC affairs.
Implementation, Review, management of affairs viz., Change Control, Deviations/CAPA, Process/ validations, product quality review, GMP/GLP training, facil...