1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
13.00 LPA TO 15.00 LPA
Position: Manager Microbiology
Location: Daman
Experience: 5 - 10 YEARS
Industries: Pharma
Responsibilities:
Experience in vaccine and biological (Mabs) manufacturing,
Handled greenfield / brownfield – Microbiology lab, qualification and validation of Microbiology lab and instruments, preparation and review of all Microbiology documents such as SOPs, protocols, reports, etc.,
USFDA and EU ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
12.00 LPA TO 18.00 LPA
Position: QC Manager (Injectable)
Location: Daman
Experience: 5 - 10 YEARS
Industries: Pharma
Responsibilities:
Experience in vaccine and biological (Mabs) manufacturing,
Handled greenfield / brownfield – QC lab, qualification and validation of QC lab and instruments,
Preparation and review of all QC documents such as SOPs, protocols, reports, etc.,
USFDA and EU audit handling exposure, ...
1 Opening(s)
0 To 3.0 Year(s)
1.80 LPA TO 2.40 LPA
1. Position- R&D Chemist/Officer2. Qualification- M. Sc /M. Pharm3. Experience-3-4 yrs.4. Responsibility? Handling of analytical instruments like HPLC, UV, titration, pH meter, Rheometer etc? Carry out the analytical development, analytical method validation or analytical workand prepare the reports for bulk, finish and rawmaterials.? Prepare stability protocols, schedules and carryout the ...
2 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 6.00 LPA
Test to a high, and continuously improving, level of GMP/GLP compliance to ensure patient safety and to minimize risk to the company business
Perform routine testing and basic GMP paperwork review with supervisor direction
Oversee the development and tracking to a plan for day-to-day testing activities to meet the daily manufacturing and ...
3 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 5.00 LPA
RM /PM Sampling, Testing and Relesing.Operation and Calibration of QC Instruments. Chemical and Physical test of Finished Good with protocol and Generate COA.Any Software Knowledge like ERP/SAP.Retain Sample Management with Records.Stability Management with testing and update records as per Schedule.Knowledge of SOP/STP/Format Related QC.All Volumetric Solution Preperation and Standardize as ...
2 Opening(s)
3.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 4.50 LPA
Job Description:? Should have strong communication skill? Handling & Calibration of instruments like HPLC, GC, KF, IR, UV, Viscosity,Tintometer? Sampling and analysis of of raw material as well as finish good? ETP sample analysis – pH, COD, TDS. MLSS , TS , TSS? Good Knowledge of physical as well as ...
2 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 2.64 LPA
A chemist studies substances at the atomic and molecular levels, conducting experiments and analysis to develop new products, processes, and knowledge. Job duties include performing qualitative and quantitative chemical analyses, developing and validating new methods, and performing quality control on products. Key responsibilities also involve writing technical reports, maintaining laboratory equipment, and ensuring ...
2 Opening(s)
0 To 1.0 Year(s)
1.20 LPA TO 1.50 LPA
Job description
Determining team priorities in accordance with the plant s needs, while coordinating with the Departmental Manager.
Sampling and analysis of RM / FG / intermediates/cleaning samples based on requirement and result in an entry in analytical sheet, QA form, and LIMS.
Perform analytical tests according to the monograph and SOP.
Responsible for ...
1 Opening(s)
15.0 Year(s) To 17.0 Year(s)
7.20 LPA TO 8.40 LPA
Preparation of Certificate of Pharmaceutical Product.
Expertise in liaising, coordinating inspections with regulatory agencies (FDA ISO 9000)
Knowledge of Microsoft Office, Microsoft Excel, ERP etc.
Goal Oriented and Results Driven Team Leader.
Expertise in writing, reviewing & approving lab procedures / documentations, Out off Specification reports, batch records, protocols, etc.
Review of QC related ...
4 Opening(s)
1.0 Year(s) To 4.0 Year(s)
2.40 LPA TO 3.60 LPA
Hiring for industrial Automation and Validation services Industry
Position: - PLC/SCADA/CSV Validation Engineer 04
Experience: - Min. 1 to 4 Years (In Pharmaceutical Company)
Qualifications: - BE/Diploma in Instrumentation/Electrical/Electronic Engineering.
Salary: 15K to 30K (depends on experience)
Job Description:
Experience in the development of validation Documents/Protocols like Validation Plan (VP), Requirement specification documents like (URS/FRS/DQ), Risk Assessment (RA), IQ, OQ, ...