Junior Quality Lab Scientist (m/w/d)

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Job Description"Caring for the world… one person at a time” … inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. This culture of caring is the focus of our corporate philosophy, that are anchored in the internationally applicable CredoJunior Quality Lab Scientist (m/w/d)(24 months fixed-term contract)Position OverviewThe Junior Quality Lab Scientist is responsible for executing and supporting the implementation of business improvement initiatives for Quality Operations Laboratories. He or she contributes to ensure compliance to JNJ and international Standards applicable to area of responsibility and drives forward the state-of-the-art direction and best practices.Tasks & ResponsibilitiesUnder and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Collaborate in Quality Operation Projects to plan, prepare, execute and/or support equipment qualification, test methods validation or computer system validation complying with local and global regulatory requirements as well as J&J standards
• If Applicable responsibility for microbiological test methods and execution
• Support Compliance Projects and implements actions which result from new standards, Non-Conformances, Audits or CAPAs
• Support and initiate Quality Operation Projects including but not limited to: Cost Improvement, System Changes, LEAN, New Software Systems, etc.
• Perform in and support Change Management Processes
• Assist the Quality Lab Scientist Supervisor in establishing the QO Laboratories projects and initiatives
• Support the Quality Lab Scientist Supervisor and other Lab Supervisors in developing, coordinating and implementing projects for improvement of processes
• Implement and Establish Data Integrity for the QO Laboratory Equipment complying with regulatory requirements as well as J&J standards
• Analyze analytical (if applicable microbiological) data for significant quality trends and report conclusions for e.g. risk based decisions or improvement processes
• Presentation of data at DRB and Management Review
• Develop expert level of knowledge for LIMS and use it for implementation or establishment of compliance or business/process improvement
• 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
• University/ Bachelor’s Degree or Equivalent in a Life Science or Engineering
• 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
• Organization for Standardization) regulations is preferred.
• Independent working habit
• Good change Management experience
• Good communication skills and team experience

Responsibility For Others & Internal Interactions

• Reports to Quality Lab Scientist Supervisor
• Regular reporting about project status
• Establishes strong connection and collaboration with business partners at the site, e.g. Quality Operations, Compliance, Manufacturing
• Participates changes in Lab Systems and Certified Operator Program
• Responsible for CAPA and NC actions
• SME for internal and external audits

Physical Working Conditions / RequirementsWhile 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 is occasionally exposed to fumes or airborne particles. The employeeperforms routine office and operations demands including computer operation. Routine office and operations including computer usage are required.LOCATION & TRAVEL REQUIREMENTSThis position may require up to 10% travel and will be based in Ethicon Norderstedt,GermanyEXTERNAL INTERACTIONS

• The position is an SME in Training and will participate in External audits when required both planned and unplanned.
• Communication with suppliers or services partners

Company DisclaimerCompany management reserves the right to add, delete or otherwise alter assigned duties at any time. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The minimum qualifications listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.Primary LocationEurope/Middle East/Africa-Germany-Schleswig Holstein-NorderstedtOrganizationJohnson&Johnson Med GmbH (7930)Job FunctionEngineering (Generalist)Job QualificationsEXPERIENCE AND EDUCATION