Engineer, Supplier Quality II

🔥 2 hours ago

🇨🇿 Czechia – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👷🏻‍♀️ Engineer

👻 Ghost score 12%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Biotechnology • Pharmaceuticals • Healthcare

Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.

📋 Description

• Support Supplier Quality operations for manufacturing sites and business units • Partner with Procurement, Quality, Operations, Engineering, and suppliers to resolve supplier quality issues • Support supplier evaluations and maintain compliant supplier quality records • Apply quality tools, supplier performance data, and risk-based thinking to improve supplier performance and protect product quality • Support and conduct supplier audits, desk audits, supplier evaluations, audit agendas, pre-meetings, and post-audit follow-up • Support NPI due diligence and supplier part qualification through PPAP requirements and supplier documentation review • Monitor supplier performance, communicate results, and drive actions to improve responsiveness and reduce risk • Engage suppliers on nonconformance, deviation, complaint, SCAR, and record-keeping activities • Support supplier problem-solving and root-cause analysis to eliminate recurrence of nonconformances • Facilitate resolution of supplier issues across suppliers, purchasing, manufacturing, Quality, and internal subject-matter experts • Document procedures, audit reports, supplier change notifications, metrics, and supplier performance reports • Collect and analyze supplier scorecards and KPIs to support improvement actions • Support Quality Agreements and PPAP documentation for supplier qualification activities

🎯 Requirements

• Bachelor's degree in Engineering, Manufacturing, Operations Management, Biological Sciences, Chemistry, Business, or equivalent combination of education and experience required for professional, management, and leadership roles • Associate degree or equivalent technical experience may be acceptable for associate roles • Quality auditor training preferred for bands 4–6; quality lead auditor training preferred or required for advanced professional roles depending on business need • Supplier audit, supplier qualification, PPAP/part qualification, supplier issue management, and corrective action experience preferred • 2–5 years of experience in Supplier Quality, Quality, Manufacturing, Operations, Engineering, Business Process, or related functions • Equivalent combinations of education, experience, and demonstrated capability may be considered based on business needs • Working knowledge of ISO 9001 and applicable industry standards • Experience with ISO 13485, 21 CFR Part 820, 21 CFR Part 210/211, ISO 14971, MDSAP, or other applicable requirements preferred based on business context • Strong written and oral communication skills • Ability to collaborate across functions and build effective relationships with suppliers, internal customers, and stakeholders • Ability to analyze data, summarize results, generate metrics, identify risks, and drive improvement actions • Detail-oriented, organized, accurate, self-motivated, adaptable, and able to prioritize work to meet business objectives • Ability to sit or stand for long periods and walk between buildings or to production, laboratory, warehouse, or office areas • Close vision needed to read documents, quality records, and computer screens • May lift up to 15–20 lbs. as business needs require • Ability to travel by air, train, or car as required; supplier-facing and leadership roles may require up to approximately 30% travel • Adherence to all Good Manufacturing Practices (GMP) safety standards

🏖️ Benefits

• Fully remote work arrangement • Standard Monday–Friday work schedule • Global work with Thermo Fisher Scientific • Potential professional development through quality auditor and lead auditor training, where applicable

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume