1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.00 LPA TO 3.00 LPA
Set Up and Operates Fitters Bay Manufacturing.
Perform Routine Maintenance and Troubleshooting
Monitor Process and Parameters to ensure consistent Product Quality.
Support Validation and Qualification of Machine, Process and Product
Maintain Documentation as per GMP and regularity standards.
Basic Knowledge of Capsule fitters, Cambridge Fitters, & In-line Disk Fitters
Immediate Joinners or 1 month Notice
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 7.00 LPA
Team Management of Qas on Transaction Audit for Branch Managers Other Verticals.
Audit Completion on Time
Timely feedback sharing with Stakeholders
Identifying Gaps and share recommendations
Identifying TNI and sharing with Training Teams
Audit the Auditor to maintain accuracy
Individual Role in driving compliance requirements with Branch Managers/Partners
Managing Compliance Case
Working on multiple compliance projects
1 Opening(s)
0 To 3.0 Year(s)
1.00 LPA TO 3.00 LPA
Location :- Bhosari
make it with us Siemens Energy is focused on helping customers navigate
the world's most pressing energy problems. As a world leader in developing
and producing the most advanced engineering technologies, we improve lives and
further human achievements worldwide, while also protecting the climate - all thanks to our employees.
With us, ...
1 Opening(s)
0 To 3.0 Year(s)
1.00 LPA TO 3.00 LPA
Live Our Vision, Values, and Beliefs every dayReports to the Customs Compliance Leader on RH's International Transportation teamTroubleshoot to resolve container holds related to customs exams and other clearance delaysSupport compliance team with HTS classifications and preparing customs paperwork
Communication All of the work we do depends on understanding what our ...
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, ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
2.40 LPA TO 3.00 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, ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: QC Officer
Location: Ahmedabad
Experience: 1 - 3 Years
Industries: Pharma
Responsibilities:
Responsible for Documentation work in QC Department.
Candidate must have knowledge of HPLC.
Shall maintained all records related to manufacturing
Overall looking after the complete filling, packing activities and Procurement of the packing material.
To ensure the compliance of safety Requirement ...
10 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 3.50 LPA
Position: Plant Operator
Location: Silvassa
Experience: 3 - 5 Years
Industries: Chemical
Responsibilities:
To run plant equipment and make sure it is operating safely and efficiently.
You may transport materials , check equipment, monitor production and keep operating record.
To work with shift chemist to fix problems or troubleshoot issues ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: QC Officer
Location: Vapi
Experience: 1 - 3 Years
Industries: Chemical
Responsibilities:
Responsible for Documentation work in QC Department
Candidate must have knowledge of HPLC & GC
Responsible for manufacturing the batch as per MOM or BMR.
Shall maintained all records related to manufacturing
Overall looking after the complete filling, packing activities and ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
1.20 LPA TO 2.16 LPA
Must Have
Environment/Pathogen Monitoring Program, Sampling & Testing of Pkg. material, raw material, finished goods, EMP sample
preparation and sterilization microbiological media, Tracking, Weekly Biological indicator test for Autoclave, growth promotion test
Should be aware of ISO & USP guideline for Microbiology. Good knowledge of GMP practices
Educational & Experience Criteria
B.Sc./M.Sc. In Microbiology