Quality Inspector

Beacon-Biosignals; Cleveland (OH); On-site; USD 38,572 - 44,083; Full time

Job summary

Beacon Biosignals in Cleveland is seeking a detail-oriented Quality Inspector to join our team. This hands-on role ensures accurate documentation, performs incoming and final inspections of components, and maintains Device History Records in line with GDP and quality system requirements.

You'll report to Quality Engineering, support audits and investigations, and help drive continuous improvement while working on-site five days a week.

Qualifications

• GDP familiarity and quality system requirements (e.g., 21 CFR 820, ISO 13485) apply to inspection and record-keeping.
• Strong attention to detail and accuracy in documentation and data recording.
• Comfortable working under established procedures and escalating issues.
• Good communication skills and ability to work well within a team.
• 1-2 years of experience performing quality inspection in a medical device or regulated manufacturing environment.

Responsibilities

• Perform incoming and final inspection of components, subassemblies, and finished devices against drawings, specifications, and work instructions.
• Record inspection results and maintain accurate records (including Device History Records) in GDP-compliant systems.
• Identify nonconforming material and escalate findings to Quality Engineering per nonconformance procedures.
• Perform monthly quality inspections of manufacturing areas to ensure SOP and work instruction compliance.
• Support Quality Engineering with document control, audits, and complaint investigations as directed.
• Assist with equipment upkeep, including flagging equipment due for calibration.
• Stay current on applicable work instructions, SOPs, and quality system requirements relevant to inspection.
• Participate in continuous improvement and quality initiatives under Quality Engineering.

Skills

Quality inspection

GDP

Attention to detail

Teamwork

Education

High school diploma or equivalent

Associate's degree in technical or scientific field preferred

Tools

21 CFR 820 familiarity

ISO 13485 familiarity

Job description

Beacon Biosignals is transforming precision medicine for the brain, from clinical development to clinical care. For Life Sciences partners, we offer the leading at-home EEG platform for clinical development of novel therapeutics for neurological, psychiatric, and sleep disorders. Our Diagnostics business is building the most comprehensive at-home platform for precision diagnostics, combining EEG and cardiopulmonary signals to deliver reimbursable assessments for sleep and central nervous system disorders. Together, we're changing the way patients are diagnosed and treated for any disorder that affects brain physiology.

What you will be doing:

We are looking for a detail-oriented, quality-focused Quality Inspector to join our Cleveland team. This role is a critical checkpoint in the manufacturing process, maintaining accurate documentation in accordance with Good Documentation Practices, and flagging nonconformances early. You'll report to Quality Engineering, supporting audits, complaint investigations, and equipment upkeep, while helping drive continuous improvement across the quality system.

This is a hands-on, in-person role ideal for someone who takes pride in precision, stays disciplined about process and documentation, and genuinely cares about product quality and patient safety.

This role is a contract role required to work from the Cleveland office 5 days a week.

$28.00 - $32.00/hour

What success looks like:

• Performing incoming and final inspection of components, subassemblies, and finished devices against drawings, specifications, and work instructions
• Recording inspection results and maintaining accurate, complete records (including Device History Records) in accordance with Good Documentation Practices (GDP)
• Identifying nonconforming material and escalating findings to Quality Engineering per established nonconformance procedures
• Performing monthly quality inspections of the manufacturing areas to ensure compliance with SOPs and work instructions
• Supporting Quality Engineering with document control, audits, and complaint investigations, as directed
• Assisting with equipment upkeep, including flagging equipment due for calibration
• Staying current on assigned work instructions, SOPs, and applicable quality system requirements relevant to the inspection role
• Participating in continuous improvement and quality initiatives under the direction of Quality Engineering

What you will bring:

• 1-2 years of experience performing quality inspection in a medical device or other regulated manufacturing environment
• High school diploma or equivalent required; Associate's degree in a technical or scientific field preferred
• Working knowledge of Good Documentation Practices (GDP) and familiarity with quality system requirements (e.g., 21 CFR 820, ISO 13485) as they apply to inspection and record-keeping
• Strong attention to detail and accuracy, particularly in documentation and data recording
• Comfortable working under established procedures and escalating issues
• Good communication skills and ability to work well within a team, taking direction from Quality Engineering

At Beacon, we've found that cultural and scientific impact is driven most by those that lead by example. As such, we're always seeking new contributors whose work demonstrates an avid curiosity, a bias towards simplicity, an eye for composability, a self-service mindset, and - most of all - a deep empathy towards colleagues, stakeholders, users, and patients. We believe a diverse team builds more robust systems and achieves higher impact.

As set forth in Beacon Biosignals’s Equal Employment Opportunity policy,we do not discriminate on the basis of any protected group status under any applicable law.

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