QC Incoming Inspector I, 2nd Shift

Anika; Bedford (MA); On-site; USD 40,000 - 60,000; Full time

Job summary

A leading company in the life sciences industry is looking for a QC Incoming Inspector for the 2nd shift. The role involves inspecting raw materials and overseeing quality assurance processes to ensure compliance with regulations. The ideal candidate will have a relevant degree and a keen eye for detail, contributing to the maintenance of product quality standards.

Qualifications

• Associates degree in life sciences or relevant experience.
• 0-1 year of experience in a cGMP facility or QA/QC role.

Responsibilities

• Perform quality line clears and in-process inspections per SOP.
• Issue lot numbers and control labels for incoming raw materials.
• Release approved raw materials for manufacturing.

Skills

Communication

Documentation

Education

Associates degree in life sciences

Bachelor’s degree preferred

Tools

Microsoft Office

ERP systems

Job description

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Summary of Primary Responsibilities:

The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture on the second shift. The position also performs inspection activities during in-process manufacturing for second shift.

Specific Responsibilities:

• Perform quality line clears and in-process inspections according to SOP requirements.
• Issue lot numbers and control labels for incoming raw materials; perform inspections per procedures.
• Release approved raw materials for manufacturing, including documentation and relabeling.
• Review MPS of other inspectors for approval and release.
• Monitor and perform annual retain inspections; coordinate retesting and document.
• Investigate OOS and participate in MRB for rejected materials.
• Serve as SME and train new employees and contractors.
• Perform biennial reviews of procedures and MPS as needed.
• Author and complete DCRs; document work activities per Good Documentation Practices.
• Maintain current training on procedures and participate in projects.

Job Complexity:

Routine assignments with detailed instructions.

Supervisory Responsibilities:

None.

Required Qualifications:

• Associates degree in life sciences or relevant experience.
• 0-1 year of experience in a cGMP facility or QA/QC role; internships considered.
• Experience with Microsoft Office or ERP systems.

Desired Skills and Knowledge:

• Bachelor’s degree preferred.
• Experience in a clean room environment.
• Strong communication and documentation skills.