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Quality Assurance Incoming Inspector Jobs in Utah

Hrmango

QUALITY ASSURANCE MANAGER

Salt Lake City, UT · On-site

QUALITY ASSURANCE MANAGER Salt Lake City area food processing facility is looking for a Quality ... Prepare for, handle, and oversee all audits (3rd party, internal) and inspections. Experience or ...

HRmango

QUALITY ASSURANCE MANAGER

Salt Lake City, UT · On-site

QUALITY ASSURANCE MANAGER Salt Lake City area food processing facility is looking for a Quality ... Prepare for, handle, and oversee all audits (3rd party, internal) and inspections. Experience or ...

Biomerics

Manager of Quality Assurance

Salt Lake City, UT · On-site

This position leads Quality Engineering and Inspection activities, oversees CAPA and nonconformance ... Partner with Supplier Quality and Purchasing to address supplier nonconformances, incoming quality ...

New

Vector

Incoming Quality Control Technician

Bluffdale, UT · On-site

$18 - $23.25/hr

... assurance. You'll work alongside experienced quality and manufacturing professionals while ... What You'll Do * Inspect incoming electronic components, printed circuit boards (PCBs), cable ...

Mars

QA Technician

Salt Lake City, UT · On-site

Quality Assurance Food Technician Day Shift -6a-6:30p SUMMARY Monitors all quality assurance/food ... Quality analysis of incoming dry goods for production. Verification of specifications before ...

Mars, Incorporated

QA Technician

Salt Lake City, UT · On-site

Quality Assurance Food Technician Day Shift -6a-6:30p SUMMARY Monitors all quality assurance/food ... Quality analysis of incoming dry goods for production. Verification of specifications before ...

Vector

Incoming Quality Control Technician

Bluffdale, UT · On-site

$18 - $23.25/hr

... assurance. You'll work alongside experienced quality and manufacturing professionals while ... Complete inspection records and maintain accurate quality documentation.Perform basic soldering ...

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Quality Assurance Incoming Inspector information

What does a quality assurance incoming inspector do?

A Quality Assurance Incoming Inspector is responsible for inspecting and verifying the quality of raw materials, components, or products as they arrive from suppliers before they are used in the manufacturing process. They check for defects, compliance with specifications, and adherence to quality standards. Their role helps ensure that only materials that meet company criteria are used, which helps prevent production issues and maintains product quality. Inspectors typically use measuring tools, review documentation, and may create reports on their findings.

What are the key skills and qualifications needed to thrive as a quality assurance incoming inspector?

To thrive as a Quality Assurance Incoming Inspector, you need strong attention to detail, knowledge of quality control standards, and often a background in manufacturing or a related technical field. Familiarity with measurement tools (calipers, micrometers), inspection software, and sometimes certifications such as ASQ Certified Quality Inspector are typically required. Excellent documentation skills, problem-solving abilities, and clear communication are essential soft skills in this role. These skills and qualifications ensure accurate verification of incoming materials, support compliance with quality standards, and help prevent defects in the manufacturing process.

What are some typical challenges faced by quality assurance incoming inspectors when evaluating new materials or components?

Quality Assurance Incoming Inspectors often encounter challenges such as identifying subtle defects in large batches, understanding complex technical specifications, and keeping up with evolving quality standards. They must work closely with suppliers and internal teams to resolve discrepancies and ensure that all incoming materials meet strict requirements. Managing time effectively to inspect high volumes without sacrificing accuracy is also a critical aspect of the role.

What is the difference between Quality Assurance Incoming Inspector vs Quality Control Inspector?

AspectQuality Assurance Incoming InspectorQuality Control Inspector
Primary FocusPrevent defects by inspecting incoming materialsIdentify defects in finished products or during production
Work EnvironmentReceiving areas, supplier sites, warehousesProduction lines, testing labs, final inspection areas
CertificationsISO 9001, ASQ certifications often preferredQuality control certifications, sometimes ASQ Certified Quality Inspector
Employer & Industry UsageManufacturing, aerospace, automotive, electronicsManufacturing, consumer goods, electronics, automotive

While both roles focus on quality, the Quality Assurance Incoming Inspector emphasizes preventing defects by inspecting incoming materials, whereas the Quality Control Inspector concentrates on identifying defects during or after production. Understanding these differences helps employers and job seekers target the right skills and certifications for each position.

What are popular job titles related to Quality Assurance Incoming Inspector jobs in Utah?

For Quality Assurance Incoming Inspector jobs in Utah, the most frequently searched job titles are:

What job categories do people searching Quality Assurance Incoming Inspector jobs in Utah look for?

The top searched job categories for Quality Assurance Incoming Inspector jobs in Utah are:

Quality Assurance Incoming Inspector jobs near you

Supervisor, Quality Assurance

DISCGENICS INC

Salt Lake City, UT • On-site

Full-time

Posted 17 days ago

Key responsibilities

  • Manage and maintain the company's Quality Management System (QMS) in compliance with cGMP.

  • Provide QA oversight for manufacturing, laboratory, packaging, and warehouse operations, including review and approval of GMP documentation.

  • Lead investigations related to deviations, OOS, OOT, and customer complaints, and manage CAPA processes.

Job description

Welcome to DiscGenics, a pioneering, late-clinical stage biopharmaceutical company dedicated to advancing regenerative cell-based therapies for patients suffering from degenerative diseases of the spine. Privately held and passionately driven, our mission is to enhance lives by alleviating pain and restoring function through innovative treatment.

At DiscGenics, we are committed to improving the quality of life for individuals debilitated by degenerative diseases of the spine. Our focus lies in developing cutting-edge therapies that offer hope and tangible results, fostering a future where patients can regain mobility and comfort.

Our team is characterized by a relentless pursuit of excellence and a nimble approach to addressing challenges. Our core values of Integrity, Innovation, Accuracy, Teamwork, and Stewardship guide everything we do.

Join us at DiscGenics and be part of a transformative journey where your contributions have the potential to impact the lives of millions. Together we innovate with purpose and compassion, striving towards a future where pain and limitations of degenerative spine diseases are a thing of the past.

Discover more about us at discgenics.com and see how you can contribute to revolutionizing patient care through regenerative therapies.

Job Summary:  

The Quality Assurance (QA) Supervisor is responsible for leading and maintaining the Quality Management System (QMS) to ensure compliance with FDA, EMA, ICH, and other global regulatory requirements applicable to biopharmaceutical development, manufacturing, testing, packaging, and distribution. This role provides quality oversight of GMP operations, manages quality systems, supports regulatory inspections, and promotes a culture of quality and continuous improvement across the organization.

The QA Supervisor partners closely with Manufacturing, Quality Control, Regulatory Affairs, Validation, Supply Chain, and Technical Operations to ensure products are manufactured and released in compliance with applicable regulations, company procedures, and quality standards.

This role interacts with all levels of the organization in a collaborative and positive way with colleagues to facilitate department and organizational initiatives for cultural cohesion aligned to the DiscGenics Values. 

Essential Duties and Responsibilities:

Quality Management System

  • Manage and maintain the company’s Quality Management System (QMS) in compliance with current Good Manufacturing Practices (cGMP).
  • Oversee quality systems including:
    • Deviations
    • CAPAs (Corrective and Preventive Actions)
    • Change Control
    • Complaints
    • Internal Audits
    • Document Control
    • Supplier Quality Management
    • Training Compliance
  • Monitor quality metrics and identify opportunities for continuous improvement.

GMP Compliance and Quality Oversight

  • Provide QA oversight for manufacturing, laboratory, packaging, and warehouse operations.
  • Ensure compliance with FDA and other applicable regulatory requirements.
  • Review and approve GMP documentation, including batch records, protocols, reports, specifications, and SOPs.
  • Assess quality risks and ensure appropriate mitigation strategies are implemented.

Investigations and CAPA Management

  • Lead and approve investigations related to deviations, out-of-specification (OOS) results, out-of-trend (OOT) results, and customer complaints.
  • Ensure timely completion of root cause analyses and effective CAPA implementation.
  • Evaluate CAPA effectiveness and monitor closure activities.

Audits and Regulatory Inspections

  • Plan, conduct, and manage internal quality audits.
  • Support supplier qualifications and vendor audits.
  • Prepare the organization for regulatory inspections.
  • Act as the primary QA representative during inspections and coordinate responses to audit findings.

Product Release and Documentation

  • Ensure proper review and approval of batch production and testing records.
  • Support product disposition and release activities in accordance with established procedures.
  • Verify the completeness, accuracy, and compliance of GMP documentation.

Leadership and Team Development

  • Lead, coach, and develop QA personnel.
  • Establish performance goals and development plans for team members.
  • Foster a quality-focused culture emphasizing compliance, accountability, and operational excellence.
  • Collaboration cross-functionally to drive quality initiatives and business objectives.

Continuous Improvement

  • Identify and implement process improvements that enhance quality, efficiency, and regulatory compliance.
  • Analyze quality trends and recommend corrective actions to prevent recurring issues.
  • Support quality risk management initiatives and inspection readiness programs.

 

Job Requirements:

  • Strong knowledge of:
  • FDA 21 CFR Parts 210, 211, and applicable regulations
  • IHC guidelines
  • GMP requirements
  • Data Integrity principles (ALCOA+)
  • Quality Risk Management 
  • Excellent problem-solving and root cause analysis skills.
  • Strong written and verbal communication skills.
  • Ability to influence and collaborate across functional teams.
  • Experience with electronic quality management systems (eQMS) preferred.
  • Experience with biologics, cell and gene therapy, monoclonal antibodies, vaccines, or aseptic manufacturing preferred.
  • Experience with computerized systems validation and data integrity programs preferred.
  • Prior experience in a commercial-stage biopharmaceutical manufacturing environment preferred.

Education and Experience:

  • Bachelor’s Degree in the Biology, Microbiology, Chemistry, Biochemistry, Pharmaceutical Sciences, Engineering, or related scientific field. 
  • A minimum of 7 years of experience in Quality Assurance within the pharmaceutical, biotechnology, or biopharmaceutical industry.
  • 3+ years of leadership or supervisory experience.
  • Experience working in GMP-regulated manufacturing environment
  • Experience supporting regulatory inspections and interactions with health authorities.


Working Conditions: 

Position requires qualified individuals to see, hear and speak (verbally and audibly). Required to ascend and descend stairs; sit, stand, lift, bend, stoop, crawl and kneel. The employee must also use hands to finger, handle or feel. Occasionally reaching with hands and arms, climbing or balancing are required. May be asked to drive or travel by car, air, or other transportation for business purposes. 

Must be able to lift and carry up to 20 pounds. 

Must be able to function effectively with noise in a lab environment. Natural and regular stressors occur on the job. 

Disclaimer: 

Please note: DiscGenics reserves the right to change, modify, suspend, interpret, or cancel in whole, or in part, any of the duties outlined above, at any time, and without advance notice to the employee.