4 Opening(s)
2.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 8.00 LPA
Hiring for Research Scientist
Designation: Research Scientist
Qualification: B.Sc. / M.Sc chemistry
Experience: Minimum 2 years in must-have experience in ADL Department.
Salary:-No bar for the right candidates.
The candidate should have experience in Method Development & Method Validation.
Job Profile:
Performs routine scientific research tasks requiring the application of standard techniques, procedures, and criteria.
Uses prescribed methods to ...
1 Opening(s)
6.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: Sr. Officer/Executive - QC
Location: Daman
Experience: 6 -8 Years
Industries: Pharma
Responsibilities:
Individually handling department & manpower.
Strong leadership skills to guide, supervise work activities, and help team members develop their skills.
Work allocation / Planning and Review of documents.
Preparation of SOP, Specification, Standard Test Procedures (STP), Raw Data ...
1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
4.00 LPA TO 10.00 LPA
1 Sampling and testing of raw materials, intermediates and finished products using currentspecification and standard test procedure for chemical testing and instrumental techniques(HPLC, IR, UV), as appropriate
2 Preparing Quality reports, including analytical reports (for raw materials and finishedproducts), Certificates of Analysis (CoA) (for finished products) and stability reports
3 Creating and ...
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)
15.0 Year(s) To 20.0 Year(s)
18.00 LPA TO 20.00 LPA
Position: Sr. Manager - QC
Location: Ahmedabad
Experience: 15 - 20 Years
Industries: Pharma Formulation
Responsibilities:
Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards.
To approve or reject, as he sees fit, raw materials, packing materials, semi finished product and finished products as per agreed/approved Specification.
To review and ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
15.00 LPA TO 20.00 LPA
Position: QC Manager
Location: Daman
Experience: 15 - 20 Years
Industries: Pharma - Formulation Responsibilities:
Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards.
To approve or reject, as he sees fit, raw materials, packing materials, semi-finished product and finished products ...
3 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 4.00 LPA
Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards.
To approve or reject, as he sees fit, raw materials, packing materials, semi finished product and finished products as per agreed/approved Specification.
To review and approve analytical reports, validation protocols, calibration reports, environmental monitoring planner and other documents of ...
2 Opening(s)
2.0 Year(s) To 12.0 Year(s)
2.00 LPA TO 12.00 LPA
Roles and Responsibilities Analytical Development lab, HPLC, LCMS, GC
Desired Candidate Profile HPLC, Analytical Skills
ADL
Roles and Responsibilities Analytical Development lab, HPLC, LCMS, GC
Analytical Method Validation as per ICH guideline.
Method development.
SOP preparation.
Stability Studies.
Method transfer.
Desired Candidate Profile HPLC, Analytical Skills
Roles and Responsibilities Analytical Development lab, HPLC, LCMS, GC
Desired Candidate Profile HPLC, Analytical Skills
1 Opening(s)
12.0 Year(s) To 15.0 Year(s)
12.00 LPA TO 15.00 LPA
Quality Control department functions for assuring the quality of all the batches manufactured,at every stage of manufacturing/processing excipients and drug products. Sampling, inspection & testing as per specifications of Raw material for release or rejection& its documentation. Sampling, inspection & testing as per specifications of packaging material for release ...