BENEFITS INCLUDE MEDICAL, DENTAL, VISION, AND LIFE INSURANCE

Pay Rate: $20.00 - $23.00/hour - Determined based on experience
Work Schedule: 100% onsite | Local candidates preferred
Note: This is a W2 only role — C2C, C2H, and W2 referrals will not be considered
BEPC is actively seeking a detail-oriented and proactive Process Quality Technician with hands-on experience in a regulated manufacturing environment to support quality assurance processes across production lines and facility areas. The ideal candidate will have a proven ability to collaborate cross-functionally and a strong background in nonconformance investigations, root cause analysis, process monitoring, and corresponding documentation in the Quality System, to ensure compliance with GMP and regulatory standards.

QUALIFICATIONS:

• Bachelor’s degree (preferred) or Technical School certification.
• High School Diploma/GED, required.
• Minimum 1+ years of experience in a GMP-regulated manufacturing environment, preferably in medical devices or pharmaceuticals.
• Proficient in ETQ Reliance, MES, ADAPTIV, Thing Worx Navigate, and other quality data systems.
• Strong understanding of quality principles, including nonconformance handling, CAPA, audit readiness, and compliance standards.
• Excellent written and verbal communication skills; able to document findings and communicate across teams.
• Demonstrated ability to work effectively in cross-functional teams and fast-paced environments.

PREFERRED QUALIFICATIONS:

• Experience supporting FDA or ISO audits.
• Working knowledge of Lean Manufacturing and process improvement techniques.
• Familiarity with training content development and e-learning systems (e.g., Compliance Wire).

• Investigate and document nonconformances (NCAs) and manage product dispositions (PDs) using electronic Quality Management Systems such as ETQ Reliance.
• Conduct root cause analyses (RCA) and implement corrective and preventive actions (CAPAs) to address quality issues and drive continuous improvement.
• Support internal and external audits and inspections, including documentation preparation, area readiness, response to observations, and execution of action plans (APs).
• Collaborate with facilities, engineering, quality assurance, and production teams to resolve process deviations and ensure adherence to GMP, ISO, and company quality standards.
• Utilize digital tools such as ADAPTIV, MES, Thing Worx Navigate, and Central Data Repository to track process parameters, maintain records, and analyze production data.
• Monitor and troubleshoot manufacturing and facilities processes to proactively identify risks and quality concerns.
• Support compliance training by creating and delivering materials (e.g., PowerPoint presentations) via Compliance Wire or similar platforms.
• Contribute to lean manufacturing and continuous improvement initiatives and promote a culture of quality and accountability in the production and facilities areas.