Position Title: Bilingual Quality Trainer
Wage: $24.00-$30.00/hour
Shift: 1st
Hours: 7:00am-4:00pm
We are seeking a hands-on Training Program Specialist to manage and improve a paper-based training system while helping to mature the overall training program within an ISO 13485-regulated manufacturing environment. The immediate priority is maintaining compliant training records, documentation, and metrics to ensure audit readiness. The longer-term focus will include developing a tiered competency model, creating bilingual English/Spanish training materials, and implementing enhanced training delivery methods. This is a temporary assignment of approximately 3 months in Lake Geneva, WI.
Responsibilities
- Maintain a paper-based training system compliant with ISO 13485 requirements, ensuring document control and traceability
- Track training completion, retraining intervals, and training effectiveness
- Maintain training metrics and reports for leadership and audit purposes
- Prepare audit-ready training records and support internal and external audits
- Assist with addressing training-related CAPAs
- Design and implement a tiered training model, including entry-level, qualified, and trainer-level
- Develop competency requirements, skill matrices, and qualification pathways
- Collaborate with Manufacturing, Quality, and HR to align training with processes, SOPs, and system changes
- Develop and administer bilingual English/Spanish training materials
- Coordinate translation and verification of training content
- Introduce and manage modern training methods such as interactive modules, videos, and microlearning while maintaining ISO 13485 document controls
- Evaluate available systems and leverage technology to improve training and qualification processes
- Utilize IQMS, where applicable, to explore integrated training and qualification capabilities
- Support continuous improvement initiatives related to employee training and qualification
Requirements
- 3+ years of experience in training coordination, quality systems, manufacturing operations, or a similar role within a regulated environment
- Working knowledge of ISO 13485 training and documentation requirements or similar quality management system standards
- Strong recordkeeping skills with a high level of attention to detail
- Strong audit-readiness and compliance mindset
- Experience developing skill matrices and competency-based qualification paths
- Strong written and verbal communication skills
- Ability to create clear, practical, and effective training materials
- Proficiency with Microsoft Office applications and comfort working with data tracking and reporting
- Preferred experience with IQMS, particularly training, qualification, or document control modules
- Preferred bilingual English/Spanish skills or experience developing bilingual training materials
- Preferred medical device or life sciences manufacturing experience
- Preferred experience creating interactive, video-based, or digital training content within a controlled/documented environment
- Highly detail-oriented, organized, and compliance-focused
- Strong ability to collaborate across Manufacturing, Quality, and HR
- Excellent communication and stakeholder management skills
- Continuous improvement mindset with the ability to quickly build structure, processes, and tools
- Strong facilitation skills and the ability to work effectively with a diverse, multilingual workforce
- Self-directed and comfortable working in a hands-on manufacturing environment
- Standard PPE is required when entering production areas
- Must follow all site safety, quality, and GMP requirements
- Background check and drug screening may be required based on site requirements
We are proud to be an equal opportunity employer.