Stellenbeschreibung:

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through 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 humanity. Learn more at https://www.jnj.com



Job Function

Technology Enterprise Strategy & Security



Job Sub Function

Data Architecture



Job Category

Scientific/Technology



All Job Posting Locations:

Norderstedt, Schleswig-Holstein, Germany



Job Description

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.




Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech




We are searching for the best talent for a Process Quality Engineer (m/w/d) to be in Norderstedt.




This position is a fixed-term contract with a duration of one year.




Internal Job Posting: 22.09. - 06.10.2025.




The Process Quality Engineer provides technical knowledge towards the identification of the causes for non-conformances and process failures, and for the implementation of the immediate, corrective and preventive actions thus compliance with all applicable regulatory requirements and company policies for the entire Business Unit manufacturing process.



Duties & Responsibilities
Under and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
• Reviews and analyses quality trends with the manufacturing team. Considering the quality trends, recommends actions for process, equipment and system improvement.
• Provides guidance to manufacturing supervisors to ensure that effective in-depth investigations are performed.
• Provides guidance within cross functional, multilevel technical teams to assure causes of non-conformance are identified and that sound corrective/ preventive actions are implemented.
• Review and actively use process and documentation Key Performance Indicators to identify improvement opportunities and drive or support activities to increase performance.
• Evaluation of the implemented corrective and preventive actions against trends to assess effectiveness of the same.
• Analysis of data and based on the trends recommends actions for process, equipment and system improvement.
• Responsible and accountable as leader of project management (e.g. CAPA lead, internal Observations lead) including managing internal and external resources
• Applies the J&J Quality procedures and Six Sigma principles
• Applies the standards of the J&J related Change Management principles
• Ensures safe working conditions and practices in the department as well as providing support on the plant safety training requirements.
• Responsible for communicating business related issues or opportunities to next management level
• For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
• Performs other duties assigned as needed


Experience And Education

At a minimum, Bachelor’s degree (Engineering or equivalent in a Life Science, Engineering, or Physical Science field). Master’s degree preferred.Experience in the QSR/ISO-regulated medical device operation preferred



REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES And AFFILIATIONS
• Distinct communication skills
• Distinct analytical thinking capabilities, prudent risk taking
• Six Sigma and/or Lean education and/or other sound statistical knowledge
• Thorough knowledge in QSR, GMP, ISO, knowledge in applied statistics and failure mode analysis techniques
• Proficient in the preparation to technical reports and presentations
• Good MS Office knowledge
• Sound knowledge about technical standards and legal requirements
• German, fluent speaking and the ability to describe complex technical topics understandable
• English, fluent speaking and the ability to describe complex technical topics understandable



At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.


Here’s What You Can Expect

• Application review: We’ll carefully review your CV to see how your skills and experience align with the role.
• Getting to know you: If there’s a good match, you’ll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.
• Staying informed: We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.
• Final steps: For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these.




Finally, at the end of the process, we’ll invite you to share feedback in a short survey — your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We’re excited to learn more about you and wish you the best of luck in the process! #RPOAMS

NOTE / HINWEIS:

EN: Please refer to Fuchsjobs for the source of your application

DE: Bitte erwähne Fuchsjobs, als Quelle Deiner Bewerbung