Your responsibilities

• Coordinating the creation, review and updates of production and QMS documentations
• Collaborating on activities related to cleanroom requalification
• Providing ongoing engineering support to production and R&D teams
• Analyzing and developing technical solutions within the scope of the project
• Participation in internal and external audits

Our requirements

• Min. 2-year experience on the similar position in quality department, in medical device industry
• Very good English is a must
• Teamwork and communication skills
• Independence, responsibility, and resistance to stress
• Ability to think analytically and solve problems

Optional

• Bachelor’s or master’s Degree, preferably in the engineering field
• Knowledge of FDA (QSR part 820), ISO 13485
• Working accurately with attention to details
• Demonstrating problem solving skills
• Creativity and an innovative approach to design
• Openness to change and a willingness to continuously learn

What we offer

• Attractive salary and additional bonus in accordance with company policy.

• Employment based on a work contract (UoP).

• Private medical care and life insurance.

• Co-financing of meals in the company cafeteria.

• Contribution to sports memberships and purchases related to sports and culture.

• Company Social Fund - subsidy for holidays, non-refundable financial assistance.

• Professional development support - possibility of receiving funding for trainings, higher education, or language learning.

• Employee Assistance Program - free and fully confidential psychological, legal, and financial counseling support for employees and their family members.