Quality Control Technician at Finish Line Staffing Services
Burlington, MA 01803, USA -
Full Time


Start Date

Immediate

Expiry Date

07 Nov, 25

Salary

25.0

Posted On

08 Aug, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Manufacturing Processes, Continuous Improvement, Excel, Corrective Actions, Materials

Industry

Pharmaceuticals

Description

SUMMARY

As a Quality Control Technician, you will be essential in maintaining high standards of quality assurance and control within our manufacturing processes. Reporting to the Quality Manager, your core responsibilities will include conducting quality audits, inspections, and analyses to ensure compliance with CGMP and FDA regulations. Your expertise in quality management systems and relevant skills with precision measuring instruments will enable you to identify defects and implement corrective actions. Join our team to contribute to the continuous improvement of our products and uphold our commitment to excellence in quality.

  • Understand the objectives, responsibilities, and mission of the Sterility & Lot Release department and work towards those goals.
  • Prioritize and plan work activities; adapt for changing conditions.
  • Review labels for accuracy and precision.
  • Review of Device History Records to perform release of sub-assemblies and finished goods.
  • Inspect finished parts, and materials for conformance to quality control standards.
  • Initiate and participate in resolution of non-conforming materials.
  • Responsible for final product release sign-off.
  • Experience in a FDA regulated environment
  • Proficient in Word & Excel
  • Knowledge of cGMP and GDP
Responsibilities
  • Understand the objectives, responsibilities, and mission of the Sterility & Lot Release department and work towards those goals.
  • Prioritize and plan work activities; adapt for changing conditions.
  • Review labels for accuracy and precision.
  • Review of Device History Records to perform release of sub-assemblies and finished goods.
  • Inspect finished parts, and materials for conformance to quality control standards.
  • Initiate and participate in resolution of non-conforming materials.
  • Responsible for final product release sign-off.
  • Experience in a FDA regulated environment
  • Proficient in Word & Excel
  • Knowledge of cGMP and GD
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