1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 6.00 LPA
Position: IPQA Officer
Location: Sarigam near by Vapi
Experience: 2 -5 Years
Industries: Pharma
Responsibilities:
USFDA, MHRM AND WHO GENEVA Audits Handling.
Handling & Monitoring of all IPQA activity
Handling & Monitor of day to day dispatch related activity
Review & Monitor ongoing validation activity
Review of EIMR & Cleaning ...
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)
6.0 Year(s) To 8.0 Year(s)
4.20 LPA TO 6.00 LPA
Position: Sr. Executive/Asst. Manager - QA
Location: Panoli - Ankleshwar
Experience: 6 - 8 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 ...
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)
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 ...
2 Opening(s)
5.0 Year(s) To 10.0 Year(s)
7.00 LPA TO 9.00 LPA
Position: Executive/Sr. Executive - QC
Location: Daman
Experience: 5 - 10Years
Industries: Pharma
Responsibilities:
Individually handling department & manpower.
Strong leadership skills to guide, supervise work activities, and help team members develop their skills.
Work allocation / Planning and Review of documents.
Preparation of SOP, Specification, Standard Test Procedures ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
15.00 LPA TO 18.00 LPA
Position: Sr. Manager/AGM - Finance
Location: Jodhpur
Experience: 15 - 20 Years
Industries: Chemical
Responsibilities:
Budgeting and Cost Control:
Prepare departmental budgets categorized by cost centers, including plant and HO budgets.
Monitor expenses, analyze variances, and initiate cost-control measures.
Develop a 5-year financial plan and ...
1 Opening(s)
12.0 Year(s) To 15.0 Year(s)
15.00 LPA TO 20.00 LPA
Position: Manager - Engineering
Location: Kheda- Ahmedabad
Experience: 12 - 15 Years
Industries: Pharma
Responsibilities:
Availability of production lines:
Monitor availability of all Machines for production.
Ensure team attends to breakdown issues on time and study MTTR (Mean time to repair) and MTBF (Mean time between failures).
As a part ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: Maintenance Manager
Location: Panoli - Ankleshwar
Experience: 8 - 10 Years
Industries: Pharma - API
Responsibilities:
To plan the efficient operation and process for technical services department and ensure their maximum uptime.
To review all the preventive maintenance plans with respect to manpower & time (planned by maintenance/Hardware/instrumentation Managers) activities for ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: RA Officer
Location: Daman
Experience: 0- 3 Years
Industries: Pharma
Responsibilities:
Preparation of the dossier as per the current prescribed guidelines of the respective regulatory authorities
Coordinate with various departments to collect the complete set of documents.
Review of the quality and analytical data as per the pharmacopoeia, ...