Quality Assurance Engineer
GForce Life Sciences
Portage, MI0–2 yrs3m agovia LinkedIn
This job at a glance
- Who can apply
- New grads and up to 2 years · Bachelor's degree
- Must know
- OperationsAuditingLean / Six SigmaExcelMicrosoft Office
- Nice to have
- Statistics
- Work
- On-site in Portage
- Pay
- Not stated by the employer.
- Skill demand
- Auditing46%Operations38%Lean / Six Sigma36%Excel25%of 99 similar entry-level jobs posted in the US this week
- Listed
- Nov 12, 2026 · still open
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About the Role
GForce Life Sciences has engaged a client to provide a Quality Assurance Engineer for a 12-month contract, onsite in Portage, MI. This role will support quality assurance, quality control, and preventive activities to ensure compliance with applicable regulations and standards.
Key Responsibilities
- Partner with Operations and business functions to support product and process quality performance.
- Collaborate cross-functionally (internal/external) to investigate and resolve quality issues.
- Own/manage internal and supplier nonconformances (NCs), including investigation and timely closure.
- Support/own CAPAs from root cause analysis through closure.
- Support disposition of nonconforming product through MRB; issue NCs as appropriate.
- Communicate with suppliers on NCs; escalate SCARs as needed.
- Support change management activities (internal and supplier) and continuous improvement of manufacturing processes.
- Create and/or review new or revised procedures.
- Maintain/analyze KPIs to monitor quality; identify trends and implement corrective actions.
- Support manufacturing complaints and product field action execution/analysis.
- Apply statistical methods for process analysis and control.
- Provide QA support during internal and external audits.
- Support process/equipment validation, qualification, and MSA activities.
- Execute quality deliverables for engineering changes, manufacturing transfers, and supplier changes.
- Support product holds and containment plans; assist with quality acceptance tests (QATs).
- Support risk management practices/tools and Lean principles (standardization, waste elimination).
- Manage supplier relationships related to performance, communications, and nonconformities.
Requirements & Tech Stack
- Bachelor’s degree.
- 0–2 years of experience in a Quality or Regulatory Affairs role.
- Familiarity with ISO 13485, GDP, and GMP concepts.
- Solid understanding of quality/engineering principles, including Risk Management, CAPA, Audits, and Statistics.
- Proficiency with Microsoft Word, Excel, and PowerPoint.
- Excellent written and spoken English.
- Willingness to work as part of a multi-site team; some travel required.
Qualifications (Nice to Have)
- Prior industry experience (desirable).
- Knowledge of risk-based thinking and statistical concepts (a plus).