(Senior) Process Engineer (m/w/d) Product Transfers - befristet auf 24 Monate

Overview

This role is a hybrid position, based out of our site in Freiburg, Germany.

• Talents we are looking for
• Goal-oriented orchestrators: People who can effectively coordinate and focus the work of peers toward an important goal, prioritizing the right activities that lead to success.
• Effective communicators: People who can interpret information clearly and accurately to concisely communicate results and recommendations to stakeholders, senior management, and their teams.
• Network builders: People who build connections with other teams and divisions and coordinate cross‑functional collaboration.

What you will do

• Provide engineering support for product transfers ensuring that all activities are completed and documented in accordance with the latest Stryker procedures.
• Determine the technical objectives of engineering assignments and make decisions regarding the direction and the results of the assignment.
• Monitor and control progress of work ensuring sound application of engineering principles and the appropriate use of policies and procedures.
• Analyze equipment to establish operating data, conduct experimental testing and result analysis.
• Mentor or be a mentee for/with others on functionally related topics.
• Ensure quality of process and product as defined in the appropriate operation and material specifications.
• Select components and equipment based on analysis of specifications, reliability and regulatory requirements.
• Work with quality engineers to develop component specific processes, testing and inspection protocols.
• Participate in PFMEA, Control Plan, SOP, PPAP and other Stryker internal process qualification generation associated with product transfers.
• Ensure adherence to GMP and safety procedures.
• Review and approve validation documentation.
• All other duties as assigned.
• Minimum Qualifications, Knowledge, Skills (Required)
• Bachelor’s degree in an engineering discipline preferred with already gained experience in a manufacturing or project environment.
• Proven track record of working in a team‑based environment.
• Excellent interpersonal skills – able to express ideas and collaborate effectively with multidisciplinary teams.
• Open‑minded with the ability to recognize good ideas.
• Innovative thinker who can envision new and better ways of doing things.
• Experience in executing complex problem‑solving techniques related to manufacturing/design technical issues.
• Good instincts and sound judgment for mechanical and structural design.
• Ability to read and interpret complex engineering drawings and understand geometrical dimensioning and tolerancing.
• Preferred Qualifications (Desired)
• Experience in the medical device industry.
• Experience in an FDA regulated or regulated industry.
• Experience of process/product validations, statistical methods, process mapping, continuous improvement and project/process improvement related experience.
• Green or Black Belt Six Sigma qualifications.
• Travel Percentage

Travel: 10%.

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