1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
7.00 LPA TO 8.00 LPA
Position: Executive/ Sr. Executive - QA (Qualification And Validation)
Location: Sarigam Near by Vapi.
Experience: 8 to 10 Years
Industries: Pharma
Responsibilities:
Led the qualification and validation of HVAC systems to ensure compliance with regulatory standards and maintain optimal environmental conditions for pharmaceutical manufacturing.
Monitor the qualification process for water systems ...
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)
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 ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.50 LPA TO 4.50 LPA
Position: Incoming Quality Engineer
Location: Sanjan Nearby Vapi
Experience: 2 - 5 Years
Industries: Engineering
Responsibilities:
Overseeing all the Quality validation documents/parameters/criteria and verifying it for the assigned department.
Overseeing all the QA activities within the assigned department, identifying areas of improvement and improving the processes wherever necessary.
Adhere to the ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
6.00 LPA TO 7.00 LPA
Position: Quality Engineer (QMS)- Line Quality
Location: Sanjan Nearby Vapi
Experience: 2 - 3 Years
Industries: Engineering
Responsibilities:
Overseeing all the Quality validation documents/parameters/criteria and verifying it for the assigned department.
Overseeing all the QA activities within the assigned department, identifying areas of improvement and improving the processes wherever necessary.
Adhere ...
2 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.50 LPA
Position: QA - Officer
Location: Silvassa
Experience: 2 – 5 Year
Industries: Pharma
Responsibilities:
Line clearance prior to Dispensing, Manufacturing, and Packaging and Validation activity.
In process check during batch manufacturing and packing as per the instructions and frequency given in the ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.50 LPA TO 4.50 LPA
Position: Jr. Officer/Officer - Microbiologist
Location: Bhopal
Experience: 3 - 5 Years
Industries: Pharma
Responsibilities:
Good Knowledge OF micro
Water validation
Area monitoring
Routine analysis of sample.
Validation of micro and preparation of protocol
Required Skills
Logical thinking.
Organizing.
Good in communication.
Required Qualification: - B.Sc/M.Sc - Microbiology
Salary :- Upto 4.50 ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 3.60 LPA
Position: QA Chemist
Location: Mehsana
Experience: 1- 3 Years
Industries: Pharma- API
Responsibilities:
Review and approve batch records, laboratory data, and other relevant documents related to the manufacturing process.
Ensure all operations comply with GMP guidelines and internal quality standards.
Conduct internal audits to assess adherence to ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: Officer/Sr. Officer - QA
Location: Vadodara
Experience: 1- 3 Years
Industries: Pharma- API
Responsibilities:
Review and approve batch records, laboratory data, and other relevant documents related to the manufacturing process.
Ensure all operations comply with GMP guidelines and internal quality standards.
Conduct internal audits to assess adherence to ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 10.00 LPA
Position: QA Manager
Location: Vapi
Experience: 8- 10 Years
Industries: Pharma
Responsibilities:
ISO/GMP Systems: Maintenance and continuous improvements in procedures and documentation, certification and compliance.
Customer registrations, Handling customer audits and complaints, CAPAs and closures.
FG/RM/PM specifications, Test plans and Customer order review
Vendor qualifications, audits and ratings.
USFDA, ...