3 Opening(s)
2.0 Year(s) To 4.0 Year(s)
1.00 LPA TO 3.00 LPA
Basic knowledge of quality control & quality department activities
calibration , temperature control , GC etc
QC documentation
sop formulation
quality analysis methods
QC standard operating procedures
lab analysis
testing , inspecting
measuring instruments
measuring products , rulers clippers, judges micrometers, micrometers
adjustment of assembly, measuring of materials
Audit documentations , appearing in Audit , CAPA
improvement of quality methods
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)
2.0 Year(s) To 6.0 Year(s)
0.00 LPA TO 0.00 LPA
We have an urgent opening for the position of Mechanical Testing Engineer for a reputed manufacturing Industry for their Navi Mumbai location.
Basic Job Description:
Responsible to carry out day-to-day testing as per documented procedure and instruction of the Technical Manager
Responsible for allocating the job to juniors/technicians and evaluating the results generated by them
Identifying the witness requirement ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 4.00 LPA
Qualification: Diploma or BE in Electronic or InstrumentationExperience: 3 to 6 Years in similar Service Field as per JD.Work: Office in Pune, Ready to travel All over India for service purpose.
Job description:Electronics PCB troubleshooting and repairs.Knowledge of Microcontroller is must.Installation and commissioning of field instruments and control Instrumentation.Onsite Troubleshooting, Repairs ...
2 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.40 LPA TO 3.00 LPA
Responsibilities
Responsible for the day-to-day operations of the pilot and main plant laboratory whilst ensuring good laboratory practices are implemented, documented and sustained
Prepare and test samples/conduct routine analysis from all phases of manufacturing with the goal of determining if the material meets the internal/external standards (accept/reject batches accordingly)
Responsible for implementing and ...
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 ...
50 Opening(s)
0 To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
R&D as chemist, sr. chemist, executive, associate research scientist/chemist, lead level R&D,
Qualification: M.sc ( Organic Chemistry )
Experience : 0 to 10 yers
Chemical Industry background is preferable.
Must be able to perform analysis from the following analytical equipment: GC, HPLC, Karl Fischer Titrator, pH Meter etc.
Analysis of raw materials, sampling of raw materials maintenance ...
4 Opening(s)
3.0 Year(s) To 4.0 Year(s)
2.50 LPA TO 3.00 LPA
Must be able to perform analysis from the following analytical equipment: GC, HPLC, Karl Fischer Titrator, pH Meter etc.
Analysis of raw materials, sampling of raw materials maintenance work record, preparation of certificate of analysis, calibration instruments etc.
Maintain all analytical equipment according to the schedule and Standard Operating Procedures (SOP’s).
Complete all ...
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 ...
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, ...