SUPERVISOR, Quality, Inspection, Test,physical labs, temporary 24 months

Johnson & Johnson; Norderstedt; Vor Ort; EUR 65.000 - 85.000; Vollzeit

Zusammenfassung

A leading healthcare company in Germany is seeking a Quality Lab Scientist Supervisor to manage and improve laboratory operations. The role involves leading a team of technicians, ensuring compliance with international standards, and implementing best practices in quality control. The ideal candidate should have a Bachelor’s degree, significant experience in a GxP regulated environment, and fluent German and English language skills. This position may require up to 10% travel.

Qualifikationen

• Knowledge of regulatory requirements (MPG, MDD, 21CFR820, ISO 13485).
• Experience in GxP regulated industry.
• Advanced computer skills and use of software applications.

Aufgaben

• Implement business improvement initiatives for Quality operations Laboratories.
• Define opportunities, analyze data with partners, and implement improvements.
• Lead the physical labs for RMQA, SFG, and FGQA.

Kenntnisse

Project management abilities

Strong communication skills

Analytical and methodical problem solving

Fluent in German

Fluent in English

Ausbildung

University/Bachelor’s Degree or Equivalent

Tools

Microsoft Office

Jobbeschreibung

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.

Job Function: Quality

Job Sub Function: Quality Control

Job Category: People Leader

All Job Posting Locations: Norderstedt, Schleswig-Holstein, Germany

Job Description:

Note for the local works council: Internal job posting from 11.12- 12.01.2026

JOB SUMMARY

The Quality Lab Scientist Supervisor - physical Labs is responsible for implementing business improvement initiatives for Quality operations Laboratories. He or she defines opportunities, analyzes data with cross functional partners and implements improvements. Ensures compliance to JNJ and international Standards applicable to area of responsibility and drives forward the state of the art direction and best practices.

The person leads the physical labs for RMQA, SFG and FGQA with two lab coordinators and around 25 lab technicians.

DUTIES & RESPONSIBILITIES

Under and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Contributes and provides project and routine leadership within the Quality laboratories
• Govern and provide all testing and release activities for the physical testing portfolio on site
• Main SME for physical test methods and execution
• Management of the lab capacity, cycle time and test result delivery
• Identifies new areas of testing techniques and software solutions that are consistent with the company’s strategic direction.
• Participates in the delivery of new lab testing efforts by using both, existing and new procedures or processes to independently interpret data and identify and correct issues.
• Proposes ideas and next steps to QO Manager and exchanges information effectively in order to reach agreement in ambiguous or sensitive situations.
• Depending on the seniority and area of the Scientist he or she leads technical groups to implement QO activities for Laborites, Certified Operator program software or microbiological solutions and solve complex problems, while complying with local and global regulatory requirements as well as J&J standards.
• 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

• University/Bachelor’s Degree or Equivalent
• Analytical and methodical problem solving
• Knowledge of regulatory requirements (MPG, MDD, 21CFR820, ISO 13485)
• Experience in GxP regulated industry
• Advanced computer skills and use of software applications

REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS

• German, fluent, native language preferred. English, fluent
• Demonstrated project management abilities
• Proficient in Microsoft Office —Word, Excel, and PowerPoint
• A thorough understanding of GMP (Good Manufacturing Practices)/ISO (International Standards)
• Independent working habit
• Advanced change Management experience
• Strong communication skills and team experience

RESPONSIBILITY FOR OTHERS & INTERNAL INTERACTIONS

• Reports to Quality Operations Manager Inspection & Test
• Regular reporting about project status
• Establishes strong connection and collaboration with business partners at the site, e.g., Quality Operations, Compliance, Manufacturing
• Acting as main point of contact for changes in Lab Systems and Certified Operator Program
• SME for internal audits
• QO specialists, lab scientists, quality specialists software application and QA project engineers report to Quality Lab Scientist Supervisor

PHYSICAL WORKING CONDITIONS / REQUIREMENTS

While performing the duties of this job, the employee occasionally is required to work in a regulated controlled manufacturing environment using company provided garments and safety equipment. The employee occasionally exposed to fumes or airborne particles. The employee performs routine office and operations demands including computer operation. Routine office and operations including computer usage are required.

LOCATION & TRAVEL REQUIREMENTS

• This position may require up to 10% travel and will be based in Ethicon Norderstedt, Germany

EXTERNAL INTERACTIONS

• Communication with suppliers or services partners