1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
Title: QC ExecutiveReporting to: Head QA
Location Turbhe, Navi MumbaiWorking Pattern - 5 Days
Responsible for: Quality control oversees of all aspects of an organization’s quality Control function. Ensures product meet corporate standards as well as all applicable government regulations.Supervises: Individual contributorWorkplace Health Safety: All Managers and Supervisors are accountable and responsible ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
4.00 LPA TO 7.50 LPA
Supervise day-to-day operations in the [lab/production/QC] department.
Ensure proper implementation of SOPs (Standard Operating Procedures).
Manage and monitor staff/workers assigned under the respective unit.
Conduct sample analysis and ensure accurate documentation of test results.
Maintain records of equipment calibration, sample logs, and QC/QA reports.
Ensure compliance with safety guidelines and company standards.
Coordinate with internal departments ...
2 Opening(s)
1.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 3.60 LPA
Responsibilities:
Adhere to Good Laboratory Practices (GLP) to ensure quality and accuracy.
Perform daily checks and calibration of lab instruments to maintain precision.
Conduct testing of veterinary products (both raw materials and finished products).
Prepare and standardize chemical solutions according to protocols.
Utilize and maintain lab instruments including UV Spectroscopy, Gas Chromatography (GC), pH Meter, ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: QA Executive
Location: Daman
Experience: 3 - 4 Years
Industries: Packaging
Responsibilities:
Perform online quality checks: Monitor the quality of Flexible packaging and Plastics Processing PET extrusion and Thermoforming product during the production process, conduct tests, analyse data, and provide feedback to the production team.
Conduct inspections ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
5.00 LPA TO 7.00 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 ...