Manufacturing Quality Engineering (mfd)

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at

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Job Description:

This position is a 1 year contract with potential to extend (without guarantee). The anticipated base pay range for this position is 51200 - 92000 Euro.

Wage level (Tarifstufe) is equivalent to E11.

The Manufacturing Quality Engineer (m/w/d) is managing changes throughout the Life Cycle for launched products. A MQE ensure compliance with company policies and procedures and recommendation involving the implementation of regulatory requirements. Utilize the Quality technical tools process and system to support appropriate execution of the quality system. And with that the MQE supports risk management activities for product changes and guide for process changes and process deviations

Under general direction and in accordance with all applicable federal state and local laws/regulations and Corporate Johnson & Johnson procedures and guidelines you have following:

Duties & Responsibilities

• Utilize Quality Engineering tools for the effective and efficient development transfer and maintenance of products/processes throughout the product lifecycle

• Utilize quality engineering principles and problem-solving skills to develop and optimize products/processes that are aligned with the overall Quality and Business vision

• Ensure effective risk management to prevent unanticipated failure modes and ensure capability

• Develop implement and maintain the appropriate Process Control Plan in alignment with Quality Plan

• Ensure the development and validation of appropriate test methods for product and process performance process controls and process risk management

• Ensure effective quality strategies for validation

• Lead and/ or support of CAPAs

• Functions as a project member in matters relating to Quality Engineering

• Ensure effective and efficient use of Quality Engineering techniques such as risk analysis test method development statistical data analysis statistical process control and development of sample plans

• Ensure effective change control

• Ensure active and thorough investigation of quality issues and effective corrective and/or preventive action

• Support and maintain a state of inspection readiness

• Utilize the safety and environmental regulations of the facility

• Is responsible for communicating business related issues or opportunities to next management level

• The position will interact with outside organizations such as health authorities (e.g. FDA

• ANVISA etc.) and notified bodies (e.g. BSI)

• Is responsible for ensuring personal and company compliance with all Federal State local and Company regulations policies and procedures

• Performs other duties assigned as needed

Qualification

• At a minimum a bachelors degree or equivalent in Engineering Life Science Pharmacy or Physical Science

• Two years experience in a regulated healthcare industry (pharmaceuticals medical device biologics or equivalent) is desirable

• Professional / Technical Experience in:

• Manufacturing and sterilization environment desirable

• Statistical Skills (Green Belt or comparable) desirable

• Basic knowledge in Quality and Regulatory framework

• Problem Solving skills

• German fluent

• English fluent

We are offering you a diversified position with a variety of responsibilities in a dynamic and complex international environment. If you we have sparked your interest then please send us your complete online application (CV cover letter) in English.

Note for our internal works council:

Internal job posting from November 26 - December 10 2025.

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Preferred Skills: