Quality Control Technician
- Axelon Services Corporation
- New Kensington, Pennsylvania
- Full Time
Job Title: Quality Control Technician
Location: New Kensington, PA Shift hours: 6:45 AM- 2:45 PM Job Summary:
The Manufacturing Quality Release role is responsible for supporting quality assurance activities within a manufacturing environment. This position involves assisting with quality inspections, identifying and resolving process abnormalities, and ensuring compliance with regulatory standards such as Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). The role offers hands-on training and opportunities for skill development in a dynamic, safety-focused setting.
Key Responsibilities:-
Assist in identifying and resolving issues related to manufacturing process abnormalities and equipment malfunctions.
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Support product quality inspections and ensure all checks are performed in accordance with project requirements.
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Help implement and maintain quality control protocols to ensure compliance with GLP, GMP, and other regulatory standards.
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Participate in the documentation and execution of quality control plans related to medical device manufacturing.
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Assist in the implementation of laboratory chemical hygiene programs and adhere to safety protocols, including proper handling and disposal of hazardous materials.
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Contribute to validation testing and support the rollout of new products and manufacturing processes.
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Perform self-inspections to verify work accuracy and escalate issues to supervisors when needed.
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Engage in continuous learning and on-the-job training to build technical expertise and knowledge of quality systems.
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Participate in planning and prioritization activities within the assigned work area.
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Basic understanding of manufacturing processes and quality assurance practices
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Digital literacy and familiarity with documentation tools
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Attention to detail and commitment to following safety protocols
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Willingness to learn quality systems and regulatory compliance standards
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Strong problem-solving skills and interest in root cause analysis
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Ability to work independently and as part of a team
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Familiarity with Quality Management Systems (QMS) and technical documentation is a plus