4 Opening(s)
1.0 Year(s) To 5.0 Year(s)
1.00 LPA TO 4.00 LPA
Knowledge of Chemical Analysis, HPLC, GC, UV, IR, AAS, FTIR & other Lab Instruments.Able to perform routine analysis, Method Development in HPLC, GC, also perform Validations.Aware of Regulatory requirements, Basic knowledge of Documentation Audit
Having an experience 3-5 year in pharma industries / GLC, HPLC exp, audit handling local as well ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
1.20 LPA TO 3.60 LPA
Role Description:This is a full-time on-site role for a Quality Control Officer located in Vagra. The QualityControl Officer will be responsible for ensuring the consistently high quality of the company'sproducts and will be involved in the testing, analysis, and documentation of productsthroughout their development.
Must have skill:• Instrument Handling of GC, ...
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 ...
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 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 ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
1.20 LPA TO 1.80 LPA
HPLC (Operation and Troubleshooting)
stability study as per ICH Guideline.
Dissolution apparatus operation and method development.
AMV analytical method validation
analyze the Raw materials, In-process and intermediates finished product and stability samples as per respective test procedures.
To perform the daily calibration of Instruments/Equipments.
To review raw materials, in process, intermediate, finished products, packing material, stability, ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
2.40 LPA TO 3.00 LPA
HPLC (Operation and Troubleshooting)
stability study as per ICH Guideline.
Dissolution apparatus operation and method development.
AMV analytical method validation
analyze the Raw materials, In-process and intermediates finished product and stability samples as per respective test procedures.
To perform the daily calibration of Instruments/Equipments.
To review raw materials, in process, intermediate, finished products, packing material, stability, ...
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 ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: QC Analyst
Location: Daman
Experience: 3-4 yrs.
Industries: Pharma
Responsibilities:
Sampling and testing of in-process and finished product.
Responsible for analysis of FG, RM and PM as prescribed specification.
Handling instruments like HPLC, GC, ICP-MS, UV, FTIR, pH Meter, etc.
Ensure all the work is performed and document accurately & complies as internal ...
1 Opening(s)
6.0 Year(s) To 7.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: AM/Dy. Manager -QC (Reviewer)
Location: Vapi
Experience: 6- 7 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 ...