1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
9.00 LPA TO 11.00 LPA
Position: Asst. Manager – QA (Qualification & Validation)
Location: Sarigam
Experience: 10 - 12 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 (e.g., ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 4.20 LPA
Position: Executive/Asst. Manager - QA
Location: Silvassa
Experience: 2 - 10 Years
Industries: Pharma
Responsibilities:
Ensure compliance with GMP, regulatory guidelines, and quality standards in pharmaceutical formulation manufacturing.
Manage quality systems, audits, documentation, validations, and batch release while leading the QA team.
Implement and maintain Quality Management ...
1 Opening(s)
12.0 Year(s) To 15.0 Year(s)
25.00 LPA TO 30.00 LPA
Position: QA Manager
Location: Ahmedabad
Experience: 12 - 15 Years
Industries: Pharma
Responsibilities:
Ensure compliance with GMP, regulatory guidelines, and quality standards in pharmaceutical formulation manufacturing.
Manage quality systems, audits, documentation, validations, and batch release while leading the QA team.
Implement and maintain Quality Management Systems (QMS) as per USFDA, WHO-GMP, ...
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)
4.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: QC Officer
Location: Daman
Experience: 4 - 5 Years
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 (STP), ...
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)
2.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 4.00 LPA
Position: Officer - Design & Development
Location: Daman
Experience: 2 - 3 Years
Industries: Pharma
Responsibilities:
Minimum experience of extrusion should be 3 years.
Handling hot melt extrusion machine and management of manufacturing through extrusion process in core plastic products.
Planning the feature development.
Working closely with the engineering team ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: IPQA Officer.
Location: Daman
Experience: 1 - 2 Years
Industries: Pharma
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 GMP, standard operating procedures ...
1 Opening(s)
12.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Design & Development Head
Location: Daman
Experience: 12 - 15 Years
Industries: Pharma
Responsibilities:-
Create and maintain Product requirements
By speaking with the stakeholders like business owners, sales teams, and support teams regularly.
On the direction of the product owner.
By analyzing usage, complaints and market indicators.
Delivery of features
By ...
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, ...