1 Opening(s)
15.0 Year(s) To 18.0 Year(s)
15.00 LPA TO 18.00 LPA
Responsible for all over Quality control and Quality Assurance department.
Reporting to MD, General administration also man power handling with safety rules & Rules & regulation & maintaining of QC logbooks and files as per ISO norms.
Work planning & distribution. Responsible for the Preventive maintenance & calibration
Laboratory instruments.
Responsible for Analysis and ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
8.00 LPA TO 12.00 LPA
Head/ Manager - Quality Assurance - Wine/Beverages/Liquor (10+yrs experience)
Salary offered: Best among the industry
JOB TITLE: Head - Quality Assurance / Manager - Quality Assurance
DEPARTMENT: Quality Assurance
REPORTS TO: Functional Reporting: Director (s)
Work experience: 10 yrs plus experience
Education: B.Sc - Wine Technology / M.Sc-Food Technology / PG Diploma - Food Technology ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
1.80 LPA TO 2.16 LPA
Job description
Roles and Responsibilities
Perform calibration on Energy Meters and CTs, PTs and Combined CTPTs ( Electro-Technical ) in NABL accredited lab to ensure adherence to established standards of accuracy.
To maintain the laboratory workflow with Quality management system procedure in accordance with NABL 17025 Quality system
Perform Calibration at Sites all over ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
1.22 LPA TO 1.44 LPA
Job Description
Sample receipt
Recording the sample type, condition and client information
Storage of the samples appropriately
Release of sample acknowledgement email to the client
Handing over the samples to designated technicians for further processing based on the
project management plan
Sample inventory maintenance and disposal of expired samples
Daily recording of laboratory temperature/humidity logs
Qualification: Bachelors in any ...
3 Opening(s)
3.0 Year(s) To 4.0 Year(s)
2.50 LPA TO 3.00 LPA
Bulk & Finished Products analysis by UV-VIS Spectrophotometer.
Prepare Analysis Report of Bulk Products.
Prepare COA of Finished Products.
Raw Material analysis.
Calibration of Ultraviolet
Calibration of pH meter.
Operate HPLC.
Calibration of HPLC.
Responsible For all Activity of Q.C Department ,cGLP as per 21(CFR)part 11,DRA documents for export,
Ensure and review,Approval of R.M Finished Products and Stability of ...
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)
9.00 LPA TO 13.00 LPA
Requirement:
Minimum 3-5 years’ experience in a Hydro-metallurgy plant.
Must have working experience at Congo.
Should know at least one of the Congo Local Language (French/ Swahili/ Lingala/ Tshiluba).
Available to join immediately.
Managing the On Site Gold Mining Laboratory. Roles & Responsibilities are but not Limited to...Underground Mine Sample AnalysisMill Sample AnalysisWet Chemical Standards ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
1.00 LPA TO 3.00 LPA
We have an opening for a BioScience Professor in Teaching Faculty For reputed Institute in Kalyani ( West Bengal) Location
Roles & Responsibilities
Plan, evaluate, and revise curricula, course content, and course materials and methods of instruction.
Prepare materials for laboratory activities and course materials, such as syllabi, homework assignments, and handouts.
Prepare and deliver lectures to Students
Desired ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
6.00 LPA TO 8.00 LPA
Provide leadership planning and work assignment.
Drug licence application and renewable of licence in State Drug Authority for different type of Formulation.
Monitoring & Maintaining Quality Systems in the plant to meet State GMP requirements.
To organize inspection & testing of Raw Material, In-Process & Finished Products.
Planning and carrying out self-inspection of all ...
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 ...