2 Opening(s)
1.0 Year(s) To 4.0 Year(s)
2.00 LPA TO 3.00 LPA
Good analytical hand
Well experienced in wet chemical analysis
Hands-on experience of GC/HPLC/UV preferred
Aware of Good Manufacturing and Good Laboratory practices
Well versed with documentations related to a pharma laboratory.
Good analytical hand
Well experienced in wet chemical analysis
Hands-on experience of GC/HPLC/UV preferred
Aware of Good Manufacturing and Good Laboratory practices
Well versed with documentations related to ...
8 Opening(s)
2.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 6.00 LPA
Monitoring of manufacturing related activity performed in Mfg facility.To maintain proper planning, scheduling and achievement of production with optimum utilization of resources.To preparation, review and implementation of all necessary standard operating procedure(SOP).To preparation and review of batch manufacturing record and protocol.Training given to all concern persons in their respective areas.To ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Formulation development. Stability studies, raw material indent, arrange for their proper storage and maintain stock register. Batch preparation and evaluation, Documentation, product development report
Formulation development. Stability studies, raw material indent, arrange for their proper storage and maintain stock register. Batch preparation and evaluation, Documentation, product development report
Formulation development. Stability studies, ...
1 Opening(s)
0 To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
To follow good documentation practices & good laboratory practices & encourage subordinate to maintain the same.
To ensure execution of safety precautions in the laboratory.
To perform daily operation & calibration of pH meter & balance.
To maintain hplc & gc column & hplc & gc instrument.
To record daily temperature monitoring of analytical ...
2 Opening(s)
0 To 2.0 Year(s)
1.44 LPA TO 2.20 LPA
Monitors the work of manufacturing technicians and quality technicians, manages record keeping, and prepares reports for management
Works with software or websites to ensure they run properly by performing manual and automated tests during development
Ensures products meet quality standards and industry benchmarks by monitoring processes, inspecting goods and services, and proposing ...
5 Opening(s)
2.0 Year(s) To 10.0 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 ...
2 Opening(s)
2.0 Year(s) To 7.0 Year(s)
3.00 LPA TO 7.00 LPA
Generic
Implement Quality Assurance activities for Pharmaceutical at Ankleshwar adhering to standard operating procedures with optimum utilization of resources to ensure consistent good quality of products to meet with customers’ requirements, living Group’s Values and Code of Ethics.
Specific additions (if needed)
KEY ACCOUNTABILITIES
Quality Management/Continuous Improvement
Line Clearance and shop floor compliance
Assisting in Complaint ...
4 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 5.00 LPA
Good analytical hand
Well experienced in wet chemical analysis
Hands-on experience of GC/HPLC/UV preferred
Aware of Good Manufacturing and Good Laboratory practices
Well versed with documentations related to a pharma laboratory.
Good analytical hand
Well experienced in wet chemical analysis
Hands-on experience of GC/HPLC/UV preferred
Aware of Good Manufacturing and Good Laboratory practices
Well versed with documentations related to ...
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 ...