2 Opening(s)
0 To 2.0 Year(s)
2.40 LPA TO 3.00 LPA
Post Name- Microbiologist
Industry Type-Food Processing & Manufacturing
Qualification- M. Sc. Microbiology
Experience- 1-2 Year
Gender- Male
Salary- As per company Norm
Language- Hindi & English
Job Profile- Having Knowledge & Experience of;
Microbiological test-Product-FG/Running/RM and Water samples TPC, Y&M, Coliforms, EB, E.Coli, salmonella & other Pathogens
Media Preparation-BPW/Peptone/PCA/VRBA/VRBGA/EMB/MacConkey/XLD/BSA/HEA/GYE/BPA/ & Sterilization/Decontamination/Lab Fumigation/ Calibration/validation.
Microbiological Sampling/FG Sampling/RM Sampling/Air Sampling/Swab Sampling/Environment Monitoring, ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 3.60 LPA
Key Responsibilities:
QC:1. Responsibilities of Quality Control Laboratory including Instrumental Lab, Chemical Lab.2. To ensure the compliance of current Good Laboratory Practices and Standard Operating Procedures in the Q.C. Laboratory.3. To prepare the working standards as per the guidelines and pharmacopoeias.4. Review of QC documents, test protocols and analytical reports.5. To ...
5 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 7.00 LPA
Job Title - QC Officer/Executive
Job Responsibilities and required key skills :
Titration method (Peroxide value, Free fatty Acid, chemicals Standardization)
Equipment Exposure ( HPLC, GC, pH meter)
Safety Compliance
GLP compliance
Good Communication Skills
Major Responsibilities: •On time analysis & release of raw material, in process samples & finished product samples • Ontime Training completion within predefined ...
4 Opening(s)
1.0 Year(s) To 6.0 Year(s)
2.50 LPA TO 3.60 LPA
Role & responsibilities
1. Knowledge of calibration and operation of HPLC with empower software.
2. Sound knowledge of analytical method development and Analytical method validation of OVI, purity, and assay method by HPLC as per pharma guidelines.
3. Knowledge of calibration and operations of all equipment's like balance, ph meter, in analytical operation.
4. ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 3.00 LPA
We are hiring a Quality control chemist in Palanpur.
Post: Quality control chemist
Location: Palanpur
Education: Bsc. in chemistry, Msc. in chemistry.Experience: minimum 1 year in API pharmaceutical industries’.Salary: Up to 25k CTC
Required skills:Minimum 1year of experience in pharmaceutical company.Handling & calibration of instrument like HPLC, GC, KF, UV, melting point/boiling point.Sampling and analysis ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
1.00 LPA TO 4.00 LPA
Responsible for analysis as per existing specification and test method.
Responsible for preparation of relevant documents like reports of analysis, certificate of analysis and approved/ rejected of the products.
Responsible for preparation of media /solutions of standards as per SOP.
Responsible for calibration, Qualification and validation of equipments/instruments and proper documentation.
Responsible for supervision ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 5.00 LPA
Environment/Pathogen Monitoring Program, Sampling & Testing of Pkg. material, raw material, finished goods, EMP sample
preparation and sterilization microbiological media, Tracking, Weekly Biological indicator test for Autoclave, growth promotion test
Should be aware of ISO & USP guideline for Microbiology. Good knowledge of GMP practices
Responsible for Decontamination of Bio-hazard waste generated from ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 4.50 LPA
? HPLC/GC Analysis of In-process, Intermediates, raw material, packing material and FinishProduct samples as per defined test procedure.? Chemical Analysis of In-process, Intermediates, raw material, packing material and FinishProduct samples as and when required.? Sampling of intermediate, finished product and raw material samples as and when required.? To maintain Raw ...
1 Opening(s)
15.0 Year(s) To 17.0 Year(s)
15.00 LPA TO 17.00 LPA
Sr. Manager- Quality Assurance (QA QC)
Job Responsibilities?:-
Planning and execution of daily QA, QC operation activities for production in Injectable section to smooth Functioning work culture.
To prepare and review the SOPs of QA QC departments. Ensure qualification/ validation status of equipment’s
QA, QC of Internal and external Manufacturing as per SOP.
Experience of handling ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 4.50 LPA
? HPLC/GC Analysis of In-process, Intermediates, raw material, packing material and FinishProduct samples as per defined test procedure.? Chemical Analysis of In-process, Intermediates, raw material, packing material and FinishProduct samples as and when required.? Sampling of intermediate, finished product and raw material samples as and when required.? To maintain Raw ...