Quality Control Inspector I

Scorpion Therapeutics; Hopkinton (MA); On-site; USD 42,000 - 65,000; Full time

Job summary

Repligen seeks a QC Inspector I to perform in-process and final inspections of single-use assembly parts at our Hopkinton, MA facility. You will inspect visually and with measurement tools, verify labeling, document results, and flag non-conformities to uphold quality standards in a regulated environment.

Responsibilities include supporting root cause investigations and contributing to continuous improvement efforts. On-site work emphasizes safety, organization, and adherence to company policies.

Qualifications

• High School diploma or technical degree preferred.
• 0-2 years QA experience in ISO 9001 environment.
• Familiar with medical device or bioprocessing inspection standards.
• Proficient with inspection tools and basic Microsoft Office applications.

Responsibilities

• Conduct inspections using visual techniques and measurement tools.
• Verify labeling and documentation of inspection results.
• Identify and report non-conformities in a timely manner.
• Support root cause investigations for quality issues.
• Contribute to continuous improvement initiatives in QA processes.
• Collaborate with multiple departments to maintain quality standards.

Skills

QA experience in ISO 9001 environment

Education

High School diploma or technical degree preferred

Tools

Inspection tools

Microsoft Office

Job description

Role: QC Inspector I

responsible for inspection, auditing, and reporting on in-process and final inspection of single-use assembly parts at Repligen's Hopkinton, MA facility, ensuring conformance to quality standards within ISO 9001.

Responsibilities: conduct inspections using visual techniques and measurement tools, verify labeling, document results, identify non-conformities, support root cause investigations, and contribute to continuous improvement.

Qualifications: High School diploma or technical degree preferred; 0-2 years' QA experience in ISO 9001 environment; familiarity with medical device or bioprocessing inspection standards; proficient with inspection tools and basic Microsoft Office applications.

HighValue: experience with bioprocessing equipment, medical devices, or aerospace inspection practices; understanding of Good Documentation Practices; familiarity with sampling plans; work in a regulated, GxP environment.

Collaboration: liaises with multiple departments, communicates non-conformities, and supports quality improvement initiatives.

WorkSetup: on-site in Hopkinton, MA, with a focus on maintaining safety, organization, and adherence to safety and personnel policies.