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

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About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https: //www.jnj.com/innovative-medicine

We are searching for the best talent for Supervisor Optische Inspektion to be in Schaffhausen.

Purpose: Supervises experienced business enablers and/or entry individual contributors. Coordinates processes and assignments for the Manufacturing Product & Packaging Operations team and supports organizational objectives and business goals. Implements project terms to meet objectives and goals of the Manufacturing Product & Packaging Operations area. Ensures compliance with established processes for strategic plans and serves as a primary point of contact for junior team members.

You will be responsible for:
• Comply with GMP, EHS and SOX requirements and guidelines associated with the respective function
• People Management 20+ and further development of the subordinate shift operators and team coordinators.
• Support production planning (together with planning, considering resources and priorities) with a focus on the fully and semi-automated inspection systems
• Support allocation of orders and teams to the corresponding production areas
• Daily Production tours and review of the tier 1 boards, initiating measures if necessary
• Monitoring the absences of subordinate shift operators and initiate measures
• Creating, processing, monitoring and closing non-conformances (quality investigations), corrections, CPAs and change controls
• Creation of performance trends from shift data, taking into account resources and priorities and definition and implementation of countermeasures.

Qualifications

Education:
• Minimum of a Bachelor's/University or equivalent degree required; focused degree in Natural Sciences, Engineering, Information Technology, or Industrial Automation (Technical, Data Analytics or Statistical degrees) or equivalent is preferred.

Experience and Skills:
• Proven years of relevant work experience
• Experience in Operations, Engineering, Quality Assurance, MSAT or Planning
• Excellent verbal and written communication and presentation skills, with the ability to influence without direct authority, across functional teams and different levels of organization leadership
• Handling of non-conformances and contact persons regarding investigations as well as the definition of effective CAPAs

Preferred:
• Experience leading change in a Pharmaceutical and/or other cGMP manufacturing environment
• Experience in Visual Inspection

Other:
• Requires fluency in German and English (written and oral)
• Good problem-solving skills and a “can do” mentality

• Willing and able to work in 3-shift rotation.

We look forward to hearing from you!#RPOAMS