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1–2 jobs· newest first

Quality Systems CoordinatorNew
PPG · San Juan del Río, Mexico
On-site · Full-time · Mid
GMP Data Review Associate
Eurofins · Columbia, US
Full-time · Entry

+10K new in the last hour

Quality Systems Coordinator

PPG · Posted Nov 4, 2026

San Juan del Río, Querétaro, Mexico
On-site
Full-time · Mid
3+ years

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Ensure the effectiveness of PPG Mexico’s Quality Management System by driving continuous improvement initiatives, maintaining quality certifications and ensuring compliance with customer, regulatory, and business requirements across manufacturing, laboratory, and distribution operations.

Responsibilities

Monitor and update customer portals and scorecards, implementing action plans when necessary.
Maintain follow-up and communication of PPG suppliers’ internal performance scores.
Plan and coordinate internal and external audits, including auditor training and follow-up of findings and nonconformities.
Develop and deploy QMS training programs throughout the organization.
Oversee the implementation and update of tools such as FMEA, Control Plan, and Risk and Opportunity Management.

Requirements

Nice to have: FMEA
Nice to have: Control Plan
Nice to have: Risk and Opportunity Management
Nice to have: Layered Process Audit

Skills

Quality System activities IATF 16949 ISO 9001 VDA Internal Auditor ISO 19011 Advanced English

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GMP Data Review Associate

Eurofins · Posted Nov 5, 2026

Columbia, Missouri, United States
Full-time · Entry

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Ensure scientific data and laboratory reports meet quality and regulatory standards before final release.

Responsibilities

Review laboratory data packages and scientific reports to ensure completeness, accuracy, and compliance with GMP and regulatory requirements.
Verify that reported results are supported by raw data and laboratory documentation.
Identify discrepancies, documentation issues, and potential compliance concerns and collaborate with laboratory personnel to resolve them.
Assist with internal quality audits and quality system activities.
Maintain accurate records and documentation in accordance with established procedures.

Requirements

Bachelor's degree in Chemistry
Bachelor's degree in Biochemistry
Bachelor's degree in Biology
Bachelor's degree in Chemical Engineering
Bachelor's degree in Pharmaceutical Sciences

Skills

laboratory experience attention to detail written communication verbal communication

organizational skills

time‑management

proficiency with computer applications

knowledge of GMP regulations

quality system activities

scientific documentation software

computer applications

Benefits

comprehensive medical coverage
dental coverage
vision coverage
life and disability insurance
401(k) with company match

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