2 Opening(s)
3.0 Year(s) To 7.0 Year(s)
3.00 LPA TO 6.00 LPA
B R AGROTECH LTD, PANOLI
Department :- Quality Control
Designation- CHEMIST, SR. CHEMIST
Min. Qualification- B.sc/M.sc (Chemistry)
JOB RESPONSIBILITY
Key Criteria: Candidate should minimum 3 years of Experience in Agrochemical / Pesticides (Herbicide, Insecticide, Fungicide) products and their Formulations. Must be Knowledge of Kinds of Formulations in Pesticides. Also should be Knowledge of Principles ,Guidelines ,Limitations ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 6.00 LPA
Sr.No. Job Description1. Registration and analysis of GP&T Lab samples.2. Documentation and analytical result reporting in LIMS.3. Daily calibration of GP&T lab instruments and documentation as per standardoperation procedure (Balance / Halogen moisture analyzer / pH meter / KF).4. Periodic calibration of PD lab instrument and documentation as per standardoperation ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
12.00 LPA TO 16.00 LPA
Must be m.sc/ M.pharma with 15-20 Year experience in commercial Lab Pharmaceuticals products Testing
Responsible for ensuring the execution of all types of analytical activities
(related to LC-MS/MS, GC-MS/MS, HPLC, GC, ICP-MS, Wet analysis, Microbiology) including planning, work allotment, analysis, trouble shooting and reporting of the performed work.
Responsible for ensuring the optimum ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 2.50 LPA
Job Profile:-
1) Development and Stability profiling of Leachable check study.
2) Complete extractable check study of Container Closure System & leachable check study of finished product by HPLC and GCMS method.
3) Identification of unknown impurities and evaluation through toxicological assessment.
4) Performed schedule calibration of HPLC and GCMS
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: QC Manager
Location: Vapi
Experience: 8-10 YEARS
Industries: Pharma
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 ...
1 Opening(s)
0 To 1.0 Year(s)
1.00 LPA TO 1.80 LPA
Position: Trainee QC
Location: Daman
Experience: 0 - 1 Year
Industries: Pharma
Responsibilities:
Responsible for Documentation work in QC Department
Responsible for manufacturing the batch as per MOM or BMR.
Shall maintained all records related to manufacturing
Overall looking after the complete filling, packing activities and Procurement ...
3 Opening(s)
3.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 6.00 LPA
Job Description
Sampling and testing of raw materials, intermediates and finished products using current specification and standard test procedure for chemical testing and instrumental techniques (HPLC, IR, UV), as appropriate
Preparing Quality reports, including analytical reports (for raw materials and finished products), Certificates of Analysis (CoA) (for finished products) and stability reports
Prepare ...
3 Opening(s)
0 To 2.0 Year(s)
0.00 LPA TO 2.00 LPA
Internal Job Description
Education / Experience
M.Sc. Analytical/Organic Chemistry/Inorganic Chemistry
Min. 5 years’ Experience in a Quality Control/Analysis laboratory in a cGMP/ISO environment, with exposure to method development and validation activities
Technical skills &
Competencies / Language
Technical competence.
Leadership skills.
Analytical ability.
Planning ability.
Communication skills.
Problem solving.
Team building.
KEY ACCOUNTABILITIES
Analysis and approval
Sampling, analysis and ascertaining quality of raw materials, packaging ...
3 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 5.00 LPA
Analysis of Inprocess, Intermediate, Raw Material, Stability and Finished product samples as per approved specification/Test method/Protocol and recording of analytical data in to analytical data sheet.
Prepare and standardize the volumetric solution and reagent as per SOP by following the Good Laboratory practices, Good documentation practices during the analysis.
To prepare QC ...
1 Opening(s)
6.0 Year(s) To 9.0 Year(s)
7.20 LPA TO 8.00 LPA
Position: Executive/Sr. Executive - QC
Location: Vapi
Experience: 6 - 9 Years
Industries: Pharma
Responsibilities:
To maintain system compliance with respect to Good Laboratory Practice, Good Manufacturing practices and Laboratory safety Guidelines in QC department.
Responsible for planning for analysis of Finish product/Raw material/intermediates/in-process samples in ...