Working Hours: 2:00 PM - 10:00 PM (CET)

This role manages Technical Training team members to ensure the successful alignment and execution of Technical Training strategies, initiatives, and processes.

What You Will Do

• Lead and develop a team responsible for the coordination, deployment, and management of role-based technical training programs.

• EnsureQuality Key Performance Indicators (KPIs),training processes, records, and curriculacomply withregulatory requirements, quality standards, and internal procedures.

• Complete training workflow tasks within the Change Control process to ensureaccuratetraining is planned and assigned in the LMS when new or revised documents are released.

• Develop,maintain, evaluate, and continuously improve training systems, standards, and processes to ensure effective training delivery and overall program effectiveness.

• Partner with functional groups (e.g., Manufacturing, Quality, Regulatory, Compliance, HR) to incorporate functional training requirements into role-based curricula and ensureaccuratetraining assignments.

• Presenttraining performance metrics to leadership during periodic meetings and forums (e.g., Quality Systems Management Review).

• Review, approve, and execute training-related QMSchangecontrol tasks.

• Monitor and respond to changes in LMS data that mayimpactthe reliability and/or automation of training assignments.

• Update training procedures, plans, and supporting documentation asrequired

• Represent Technical Training processes during regulatory audits and inspections, providing training records and qualification evidence as needed.

• Provide support for NC/CAPAs related to training outcomes or training processes.

• Performadditionalduties andprojects asassigned.

What You Will Need

Required

• Bachelor’sdegreein Business, Education, Human Resources, or related discipline.

• Minimum of 5 years of experience in medicaldevice,supporting quality, compliance, manufacturing, operations, or technical training programs.

• Experience managing one or more remote team members.

• Ability towork with repetitive, detail-oriented tasks that require a high degree of accuracy

• Strong understanding of QMS requirements

• Experience ininteracting with regulatory agencies (FDA, MoH, TUV, etc.)

• Fluent in written and oral English – C1 Level (writing documents, meeting minutes, conference calls, etc.)

• Knowledge of Good Manufacturing Practices (GMPs) and ISO 13485 regulations.

• Well versed with MS Office tools such as Word and PowerPoint; highly proficient with Excel spreadsheets.

Preferred

• Experience supporting training programs within manufacturing, supply chain,logistics, procurement, or sales operations environments.

• Knowledge of training needs analysis, instructional design, adult learning principles, training evaluation methods, and eLearning development.

• Demonstrated ability to deliver instructor-led training ata high level

• Demonstrated ability to work well in a fast-paced environment.

• C1German language skills (written and spoken)