3 Opening(s)
1.0 Year(s) To 5.0 Year(s)
1.00 LPA TO 3.00 LPA
Knowledge of good Laboratory practices & STD sampling procedures.
Knowledge of ink / paints, various testing procedures & RM / FG testing methods.
Operational knowledge of lab instruments, Spectrophotometer, GLC, Karl fisher, Viscometer etc.
Awareness of safety, MSDS.
Systematic approach and Planning abilities
Exposure to ISO-(QMS, EMS, OHSAS) & TPM
Working experience of SAP modules.
3 Opening(s)
0 To 2.0 Year(s)
0.00 LPA TO 1.20 LPA
Conducting experiments using proper lab equipment
Preparing and testing solutions
Analyzing and reporting on test results
Laboratory work is a plus
Hands-on experience with spectrometer and chromatography instruments and techniques
Good knowledge of laboratory health and safety standards
Excellent analytical and research skills
Attention to detail
BSc in Chemistry
Customize formulas and use different reagents to test chemical reactions
Write ...
4 Opening(s)
1.0 Year(s) To 5.0 Year(s)
1.00 LPA TO 4.00 LPA
Knowledge of Chemical Analysis, HPLC, GC, UV, IR, AAS, FTIR & other Lab Instruments.Able to perform routine analysis, Method Development in HPLC, GC, also perform Validations.Aware of Regulatory requirements, Basic knowledge of Documentation Audit
Having an experience 3-5 year in pharma industries / GLC, HPLC exp, audit handling local as well ...
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, ...