1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
1.80 LPA TO 3.60 LPA
Maintain and upgrade quality level of products and services by Effective implementation of Quality management system and related approvals such as API 6D, ASME, OHAS, and other approvals Ensure product is meeting customer requirements by converting order specific customer requirements by implementing robust system
Devises sampling procedures and designs and develops ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: Executive/Sr. Executive - QA
Location: Vapi
Experience: 2 - 4 Years
Industries: Pharma - Formulation
Responsibilities:
Responsible for document and data control activities
To prepare and update all master document list as per requirement.
To initiate change control/document amendment for any change or improvement in the ...
2 Opening(s)
10.0 Year(s) To 20.0 Year(s)
Not Disclosed by Recruiter
Position Summary:
Performs cost estimating, analysis, and control activities, as directed
Reports to and receive technical and operational supervision from designated supervisory personnel.
Provides technical direction to assigned personnel, when delegated.
Maintains relationships with project personnel, particularly with individual discipline group leaders and engineers.
Basic Qualifications:
Knowledge in capital cost and services cost.
Knowledge of scope change ...
2 Opening(s)
4.0 Year(s) To 10.0 Year(s)
Not Disclosed by Recruiter
Position Summary:
Performs cost estimating, analysis, and control activities, as directed
Reports to and receive technical and operational supervision from designated supervisory personnel.
Provides technical direction to assigned personnel, when delegated.
Maintains relationships with project personnel, particularly with individual discipline group leaders and engineers.
Basic Qualifications
Knowledge in capital cost and services cost.
Knowledge of scope change ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
4.00 LPA TO 6.00 LPA
Quality Assurance Specialist Responsibilities:
Ensure product quality and conformity to regulatory standards, including Medical Device Regulation (MDR) and Quality Management System (QMS).
Conduct internal quality audits and participate in management review meetings.
Handle investigations of complaints and implement corrective and preventive actions.
Maintain and update quality manuals, formats, and standard operating procedures (SOPs) in ...