Supervisor QC Equipment Lifecycle Management

<p><span>At Johnson &amp; 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</span></p><p></p><p></p><p><b><span><span>Job Function: </span></span></b></p>Quality<p></p><p></p><p><b><span><span>Job Sub </span></span><span><span>Function: </span></span></b></p>Quality Systems<p></p><p></p><p><b>Job Category:</b></p>People Leader<p></p><p></p><p><b>All Job Posting Locations:</b></p>Leiden, South Holland, Netherlands<p></p><p></p><p><b>Job Description:</b></p><p><br/><b>THE OPPORTUNITY</b><br/><br/><span>Janssen Biologics is currently recruiting a </span><b>Supervisor QC ELM </b><span>within our Quality Control (QC), which has a key role in supporting the testing teams by maintaining and introducing the required automation tools, laboratory systems and equipment. The whole automation team consists of approximately 9 FTE’s direct reports as part of the <b>Qc Lab Services department.</b></span></p><p></p><p><b>About the Company:</b></p><p></p><p><b>Janssen Biologics B.V</b>. is one of the Janssen Pharmaceutical Companies of Johnson &amp; Johnson, and is passionate about the development, production and marketing of vaccines and antibodies to prevent and combat infectious diseases. At the <b>Leiden Site</b>, <span>dedicated and multi-scaled people are working in a dynamic culture in which innovation and a 'can do' state of mind are key.</span></p><p>The<b> Janssen Supply Chain</b> include the Leiden <b>QC large molecule laboratory</b>, which is divided into various testing laboratories and supporting departments based on specific techniques and expertise. One of the unique features of Leiden QC is its role as global HUB for stability testing. The test labs receive support from the Lab Services Team, which provides a wide range of services.</p><p><b>As a QC ELM Supervisor, you will be responsible for the following tasks:</b></p><p></p><p><b><span>Technical and job specific</span></b></p><ul><li>Supervise the ELM team and ensure that all departmental activities are carried out in accordance with company policies, procedures, and regulations.</li><li>Manage the ELM activities and projects, including system installation, validation, and maintenance, to ensure that all work is completed on schedule and within budget.</li><li>Participate in cross-functional teams to support process improvements, product transfers, and investigations related to automated systems.</li><li>Collaborate with other departments, such as Quality Control, Quality Assurance, Manufacturing, and Engineering, to ensure that automation systems are integrated and aligned with business objectives.</li><li>Ensure the team is subject matter expert in equipment validations and has a leading role during the GMP inspections.</li><li><span>Oversee communication between internal and external parties during the analytical equipment implementation process.</span></li><li><span>Take the lead in ELM improvement initiatives and projects, in cooperation with the global organization and in alignment with business needs. </span></li></ul><p></p><p><b><span>Managerial</span></b></p><ul><li><span>Mentors, coaches, trains, and develops the personnel on the team, evaluates performance, and provides opportunities for growth. </span></li><li><span>Manages the planning and resource allocation of the team. Prioritize, escalate, and ensure the stakeholders are aware of the deliverables and timelines.</span></li><li><span>Create a team environment that fosters continuous improvement and critical and creative thinking.</span></li></ul><p><span>Finally, you will also be responsible for ensuring compliance with relevant regulations and guidelines related to safety, health, environmental procedures, data generation and maintenance in accordance with current regulatory requirements.</span><br/><br/> </p><p><b>We would love to hear from YOU, if you have the following essential requirements: </b></p><ul><li>Master’s degree in Life Sciences / Chemistry / Biotechnology or highly experienced in a similar position.</li><li>Planning skills, ability to prioritize multiple commitments</li><li>Minimal 4-6 years of work experience in Pharma with GMP and automation or engineering experience</li><li>Project Management or people management experience</li><li>Laboratory Experience is considered as a plus.</li><li>Ability to engage with personnel at all levels within the organization, to build and maintain fruitful relationships</li><li>Written and oral communication skills in English. Dutch is desirable</li><li>Pro-active, works independently