Saltera Group
Saltera HR is proud to partner with a medical device manufacturing organization operating in a clean, high-precision environment where quality is non‑negotiable. The Quality Inspector plays an essential role in ensuring that every product leaving the facility is safe, compliant, and built to the exact standards required for patient use.
This role is hands‑on and detail focused. It is a strong fit for someone who takes pride in careful work, consistency, and doing things right the first time.
What You Will Do Inspection and Quality Control
Perform visual and dimensional inspections during and after production
Use microscopes, calipers, micrometers, gauges, and precision measurement tools
Identify and document non‑conformances and assist in root cause and corrective action processes
Maintain accurate inspection logs and production records
Manufacturing Support
Operate and monitor production equipment to maintain accuracy and output
Package, label, and prepare finished products to meet regulatory requirements
Partner with Production, Quality, and Engineering on continuous improvement efforts
Compliance and Safety
Follow GMP, CGMP, FDA, ISO 9001/13485, and internal SOPs
Maintain cleanroom standards, including proper gowning and contamination control
Promote and practice safe work habits at all times
What You Bring
Experience in medical device or pharmaceutical manufacturing preferred
Hands‑on familiarity with cleanroom work, quality inspection, and process documentation
Working understanding of FDA, ISO 13485, and GMP compliance standards
High attention to detail, strong communication skills, and comfort following defined procedures
Mechanical aptitude and comfort learning equipment and inspection tools
Basic proficiency in Microsoft Office and data entry systems
What Success Looks Like
Accurate, timely inspections and documentation that maintain regulatory compliance
Consistent product quality with reduced non‑conformance occurrences
Smooth communication between production and quality teams
Active contribution to process and product improvements
Work Environment
Cleanroom setting with gowning requirements and strict hygiene standards
Standing and performing hands‑on work for extended periods
Use of microscopes and small precision instruments
Climate‑controlled, structured production environment
EEO Statement Saltera HR is proud to partner with organizations who value people. We support workplaces grounded in respect, safety, and equal opportunity. All qualified applicants will be considered.
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This role is hands‑on and detail focused. It is a strong fit for someone who takes pride in careful work, consistency, and doing things right the first time.
What You Will Do Inspection and Quality Control
Perform visual and dimensional inspections during and after production
Use microscopes, calipers, micrometers, gauges, and precision measurement tools
Identify and document non‑conformances and assist in root cause and corrective action processes
Maintain accurate inspection logs and production records
Manufacturing Support
Operate and monitor production equipment to maintain accuracy and output
Package, label, and prepare finished products to meet regulatory requirements
Partner with Production, Quality, and Engineering on continuous improvement efforts
Compliance and Safety
Follow GMP, CGMP, FDA, ISO 9001/13485, and internal SOPs
Maintain cleanroom standards, including proper gowning and contamination control
Promote and practice safe work habits at all times
What You Bring
Experience in medical device or pharmaceutical manufacturing preferred
Hands‑on familiarity with cleanroom work, quality inspection, and process documentation
Working understanding of FDA, ISO 13485, and GMP compliance standards
High attention to detail, strong communication skills, and comfort following defined procedures
Mechanical aptitude and comfort learning equipment and inspection tools
Basic proficiency in Microsoft Office and data entry systems
What Success Looks Like
Accurate, timely inspections and documentation that maintain regulatory compliance
Consistent product quality with reduced non‑conformance occurrences
Smooth communication between production and quality teams
Active contribution to process and product improvements
Work Environment
Cleanroom setting with gowning requirements and strict hygiene standards
Standing and performing hands‑on work for extended periods
Use of microscopes and small precision instruments
Climate‑controlled, structured production environment
EEO Statement Saltera HR is proud to partner with organizations who value people. We support workplaces grounded in respect, safety, and equal opportunity. All qualified applicants will be considered.
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