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The Sales Manager is responsible for driving revenue growth and managing sales in Czech Republic and Slovakia by developing market strategies, leading a sales team, and maintaining relationships with key stakeholders.

The role involves expertise in MES, including management, project implementation, user training, and ensuring compliance in manufacturing operations.

As a Senior Quality Engineer, you will ensure compliance across the Quality Management System and products, improve processes, support audits, and provide training to stakeholders in the regulated medical device environment.

The Senior System Analyst will analyze, design, and oversee business application solutions, focusing on quality management while driving improvements and efficiency.

The PLM Lead drives product lifecycle management across the portfolio, ensuring demand alignment, facilitating stakeholder consensus, and training team members for effective supply chain execution.

The Prior Authorization Specialist verifies insurance eligibility and coverage, calculates out of pocket estimates, submits documentation, and communicates effectively with customers and insurance payors to ensure reimbursement for hearing devices.

The Technical Communications Coordinator manages labelling and documentation for regulatory submissions and product launches, ensuring accuracy and compliance in collaboration with cross-functional teams.

The Technical Writer will create and maintain product labeling for hearing implant devices, ensuring compliance with international standards and collaboration with cross-functional teams.