1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 2.50 LPA
Job Description• To perform IPQA activities at shop floor in each and every stage of sterile manufacturing and packing.• QA overview for clean room behavior and aseptic activity.• Review of batch processing records.• Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release.• Review ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 2.40 LPA
Job description:
Responsible for overseeing manual production methods to make sure that the desired product yield is achieved.
Responsible to maintain and improve housekeeping in all areas within the department.
Ensure final product meets quality and customer specifications.
Ensure that all products are manufactured with utmost efficiency and quality, according to planned protocols using ...
4 Opening(s)
3.0 Year(s) To 8.0 Year(s)
2.50 LPA TO 5.00 LPA
Job description:
Responsible for overseeing manual production methods to make sure that the desired product yield is achieved.
Responsible to maintain and improve housekeeping in all areas within the department.
Ensure final product meets quality and customer specifications.
Ensure that all products are manufactured with utmost efficiency and quality, according to planned protocols using ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 15.00 LPA
Responsible for manufacturing operations & new compound developments in plant
Undertaking feasibility studies for improvement in production methods/equipment for better quality, safety & economy.
Responsible for execution of installation, commissioning, validation activity of formulating equipment with coordination with internal & external agencies.
Designing manufacturing layout and managing erection and commissioning activities of instruments, ...
1 Opening(s)
3.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 15.00 LPA
Analyze and interpret test results.
Conduct chemical, biological and physical tests.
Effectively collect samples and specimens.
Conduct mathematical calculations.
Maintain laboratory equipment.
Use computers and a variety of computer software programs.
Prepare clear, concise and technical reports.
Lead, organize and review the work of lower level staff.
Respond to emergency situations.
Communicate clearly and concisely, both orally and in ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 3.00 LPA
1.Quality Control functions in Pharmaceutical manufacturing facility.
2.Testing and analysis of various raw materials and finished products.
3.Must be versatile with documentation as per GMP (Good Manufacturing Practice) including preparation of BMR, Analytical documents and other relevant statutory procedures.
4. Should have hands-on experience with statutory compliances, analytical instruments, with good knowledge of ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
2.10 LPA TO 3.60 LPA
Receiving Monthly & daily Production plan from Production Manager.
Manufacturing of batch as per MBR.
Temperature & Relative Humidity monitoring in manufacturing area.
Maintaining logbooks(General cleaning logbook,Equipment calibration & cleaning logbook,).
Preparation of daily production & manpower Record.
Online the Batch Manufacturing Record (BMR).
In process checks of all stages of manufacturing & packing of Tablet, ...
5 Opening(s)
0 To 4.0 Year(s)
1.20 LPA TO 1.80 LPA
Post: Lab Chemist
Qualification: BSc Chemistry and above
Company Profile: Gradually the company expanded its customer base to include Electrical Switchgear industries.
It was in the year 2004, that the company expanded its product range to include electrical enclosures like MCB distribution boxes, Concealed metal boxes and main switches.
Today, after 25 years the company has grown to a full-fledged manufacturing ...
1 Opening(s)
6.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 6.00 LPA
Post: Quality Lab Chemist
Education: Bsc / Msc Chemistry
Experience: Min 5 Years in Steel Industry / Rolling Mill
Job Assignment in Lab :
• Checking the specification percentage in the coolant, measuring the oil concentration, Checking the Cl, Fe Percentage in mill Process, Inspection the Final Rolling On Mill Process.
•Checking the CGL Line Zink Bath Testing
•Daily Reporting Process Control, Reporting The SOP Process
•Working In 5 ‘S’ Process
Job Assignment in CGL line:
•Checking the steel sheet, Checking Hardness HRB & VPN, Bend testing, LFQ (long farming testing), measuring the thickness & width, Defects on Sheet, Checking the Zinc Coating, Checking The I Value.
•Clearing the Quality CGL Line in SAP
•Reporting the SOP Process
Job Assignment In CRM Line:-
•Checking the steel sheet, Checking Defects on Sheet, Measuring the thickness & width.
•Clearing the Quality CRM Line in SAP.
•Reporting the SOP Process.
Water Test: PH, Alkalinity Hardness, Conductivity, Chloride, HCN, Total NH3, Phenol, C.O.D., B.O.D.,D.O, Oil & Grease, Mlss, Mlvss, TDS, SS, Sulphaide, Phosphate.
By Product: Tar Moisture, Tar Dust & Tar Fog, TI, and BI.
Gas Analysis orsat apparatus CO2, CmHn, O2, CO, CH4, and H2.
Estimation of NH3, H2S, Naphtha.
Coke & Coal Ash: Estimation of Coke & coal ash:
SiO2, Al2O3, CaO, MgO.
Job Location: Chitegaon MIDC, Aurangabad Maharashtra
for more details call on 7249840333 / 9765567506
1 Opening(s)
Not Mentioned To 1.0 Year(s)
1.44 LPA TO 1.80 LPA
Lab Assistant:
B.Sc. Chemistry.
Exp. 0 – 1 yr
Salary up to 10 – 12 K
Excellent spoken/verbal English is required.
Morning and afternoon shifts
Any one day in week is off
B.Sc. Chemistry.
Exp. 0 – 1 yr
Salary up to 10 – 12 K
Excellent spoken/verbal English is required.
Morning and afternoon shifts
Any one day in week is off