1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: QC Manager
Location: Vapi
Experience: 8-10 YEARS
Industries: Pharma
Responsibilities:
Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards.
To approve or reject, as he sees fit, raw materials, packing materials, semi finished product and finished products as per agreed/approved ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 7.00 LPA
JD For icpms
l Perform chemical analysis using ICP-MS and AAS for a diversity of applications.
Familiarity with GLP and ISO 17025 quality system standards.
l Expert in sample Preparation for metal analysis..
Having Good Experience in metal analysis in food and water.
l Develop and validate ICP-MS methods in support of API and/or drug ...
4 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 5.00 LPA
Good analytical hand
Well experienced in wet chemical analysis
Hands-on experience of GC/HPLC/UV preferred
Aware of Good Manufacturing and Good Laboratory practices
Well versed with documentations related to a pharma laboratory.
Good analytical hand
Well experienced in wet chemical analysis
Hands-on experience of GC/HPLC/UV preferred
Aware of Good Manufacturing and Good Laboratory practices
Well versed with documentations related to ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
5.00 LPA TO 6.50 LPA
Position: Executive - QA (QMS)
Location: Ahemdabad
Experience: 4 to 5 year
Industries: Pharma
Responsibilities:
Conduct quality assessments and audits of processes, products, and systems.
Ensure compliance with GMP, GLP, and regulatory requirements within the pharmaceutical sector.
Implement and maintain digital quality assurance processes and tools.
Collaborate with ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
1.80 LPA TO 4.50 LPA
We have urgent opening for QC Officer.
Location - Bharuch
Experience - Minimum 2 yr
Job Description -
QUALITY CONTROL OFFICER
1) No. of Person – 01
2) Role Description: This is a full-time on-site role for a Quality Control Officer located in Vagra. The Quality Control Officer will be responsible for ensuring the consistently high ...
1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 20.00 LPA
Position: QC Manager
Location: Ahmedabad
Experience: 10 - 12 Years
Industries: Pharma - Formulation Responsibilities:
Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards.
To approve or reject, as he sees fit, raw materials, packing materials, semi-finished product and finished products ...
2 Opening(s)
1.0 Year(s) To 4.0 Year(s)
2.00 LPA TO 3.00 LPA
Good analytical hand
Well experienced in wet chemical analysis
Hands-on experience of GC/HPLC/UV preferred
Aware of Good Manufacturing and Good Laboratory practices
Well versed with documentations related to a pharma laboratory.
Good analytical hand
Well experienced in wet chemical analysis
Hands-on experience of GC/HPLC/UV preferred
Aware of Good Manufacturing and Good Laboratory practices
Well versed with documentations related to ...
2 Opening(s)
1.0 Year(s) To 4.0 Year(s)
2.00 LPA TO 3.00 LPA
Good analytical hand
Well experienced in wet chemical analysis
Hands-on experience of GC/HPLC/UV preferred
Aware of Good Manufacturing and Good Laboratory practices
Well versed with documentations related to a pharma laboratory.
Good analytical hand
Well experienced in wet chemical analysis
Hands-on experience of GC/HPLC/UV preferred
Aware of Good Manufacturing and Good Laboratory practices
Well versed with documentations related to ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Job Title: ElectricianLocation: AhmedabadSalary: Best in Industry (It will be on Talisman HR Solutions Payroll)Working Days: 26 days/monthShift: FlexibleQualification: ITI Electrical / Diploma in ElectricalExperience: 3-5 yearsFacilities: Double OT & transportation within Ahmedabad
Key Responsibilities:
Perform preventive and breakdown maintenance of electrical equipment.
Maintain OSD equipment (RMG, Coating, Compression, FBD, etc.).
Adhere to GxP ...
1 Opening(s)
3.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
Former experience in the following:
Working in Medical Device: Initiate, monitor, and verify the effective implementation of the Quality Management System in all areas of company activities
Regulatory submissions: Regulations requirements of the ISO 13485; FDA; CE (MDD/MDR) and MEDDEV
Composing and maintaining quality manual procedures (i.e., SOP’s), Follow the requirements of GLP/GMP.
Internal ...