31 Job openings found

3 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 3.00 LPA
 Position:          Production Chemist (DCS) Location:          Mehsana Experience:       1 - 3 Years Industries:        Pharma    Responsibilities:         Knowledge of BMR Specification, GMP compliance, Area Clearance, process check and batch result, troubleshooting, Co-ordination with QC/QA & other dept. Responsible for manpower work distribution in shift ...
4 Opening(s)
Not Mentioned To 1.0 Year(s)
1.00 LPA TO 1.50 LPA
Qualification: Bsc / Msc in chemistry with 0 to 2 yrs experience in micro chemist profile. Ready to work at Boiser location in Maharashtra Professional Skills : Self confident and hard working. Ability to work independently as well as part of team. Willingness and ability to pick up new technical skills. Ability to adapt any work ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
1.44 LPA TO 1.54 LPA
Job description Packing Chemist Officer Female 1 1 to 2 12th/BA Salary : 12000 to 13000 Location : Dadra & Nagar Haveli Required Candidate profile packing officer / supervisor having experience Perks and benefits As per industry Role Production & Manufacturing - Other Industry Type Pharmaceutical & Life Sciences Functional Area Quality Assurance Employment Type Full Time, Permanent Role Category Production & Manufacturing Education :  12th/BA UG :Graduation Not Required, Any Graduate
15 Opening(s)
2.0 Year(s) To 15.0 Year(s)
2.00 LPA TO 10.00 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 ...
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 ...
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, ...
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 ...

Drop Your CV

We will consider your Profile for future Jobs

Submit Profile