1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
Location: IMT Faridabad Plant
Education:
A B.Sc. degree preferably in Chemistry, or diploma in related filed.
A solid background and understanding of Chemistry is mandatory
Computer proficiency- Microsoft Office , especially Excel
Experience working in contract Laboratory considered an asset.
Experience working with Pharmaceuticals
Job description:
Proficient in operating GC/HPLC/LC-MS/MS/GC-MS.
Ensures that all work is carried out in compliance ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
Not Disclosed by Recruiter
Experience of handling of analytical instruments such as HPLC, UV, Dissolution etc.
Wet analysis experience
Purified water testing experience (if any).
Knowledge and understanding of Good documentation and Good Laboratory practices
Knowledge of pharmacopoeia
Other Details:
Payroll company- Talisman HR Solutions PVT LTD (Third Party)
Work timing - 08:00 am - 05:00 pm
Work Days - Mon - Fri
Job ...
2 Opening(s)
2.0 Year(s) To 4.0 Year(s)
4.80 LPA TO 6.00 LPA
Description:
Assist Chemist in planning and executing laboratory tests according to test procedures. Conduct chemical experiments under the guidance of Head Chemist. Document test procedures and results and report the same to Head Chemist for analysis.
Manage an analytical laboratory, which include SEM-EDS, GC-MS, GPC, FT-IR, ICP-MS, TGA and DSC equipment.
Manage projects ...
15 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Sampling of all raw materials, packing material, finished product as per their sampling plan.
Testing of all raw materials, packaging materials, in-process products & finished products.
HPLC/GC analysis of in process & FG & its documentation, as well as calibration of HPLCs/GCs and balance. Handling the head space analysis. Additionally, can perform ...
15 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Sampling of all raw materials, packing material, finished product as per their sampling plan.
Testing of all raw materials, packaging materials, in-process products & finished products.
HPLC/GC analysis of in process & FG & its documentation, as well as calibration of HPLCs/GCs and balance. Handling the head space analysis. Additionally, can perform ...
1 Opening(s)
0 To 2.0 Year(s)
1.80 LPA TO 2.00 LPA
Position: QC Chemist
Location: Mehsana
Experience: 0 -2 Years
Industries: Pharma API
Responsibilities:
Responsible for Documentation work in QC Department
Candidate must have knowledge of HPLC/GC
Responsible for manufacturing the batch as per MOM or BMR.
Shall maintained all records related to manufacturing
Overall looking after the complete filling, packing ...
5 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Sampling of all raw materials, packing material, finished product as per their sampling plan.
Testing of all raw materials, packaging materials, in-process products & finished products.
HPLC/GC analysis of in process & FG & its documentation, as well as calibration of HPLCs/GCs and balance. Handling the head space analysis. Additionally, can perform ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 6.00 LPA
Position: QC Chemist
Location: Vatva - Ahmedabad
Experience: 4 - 6 YEARS
Industries: Chemical
Responsibilities:
To conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods or stability samples.
To calibrate, validate, or maintain laboratory equipment.
To compile laboratory test data and perform ...
5 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 5.00 LPA
Sampling of all raw materials, packing material, finished product as per their sampling plan.
Testing of all raw materials, packaging materials, in-process products & finished products.
HPLC/GC analysis of in process & FG & its documentation, as well as calibration of HPLCs/GCs and balance. Handling the head space analysis. Additionally, can perform ...
1 Opening(s)
7.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: Manager/Dy.Manager -QC (Reviewer)
Location: Daman
Experience: 7-10 Years
Industries: Pharma formulation
Responsibilities:
Review and evaluate QC test results,
analyse data and related records generated by QC Team,
identify discrepancies and deviations,
analyse and resolve deviations,
compliance with regulatory requirement, handle OOS, OOT,
Have handled HPLC
preventive maintenance of lab equipment,
take ...