Manufacturing Manager - 2nd Shift
DiaSorin - northbrook, IL
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Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world. Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist." Why Join Diasorin? Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world. Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry. Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive. Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward. Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact! Job Scope: We are seeking a dedicated and experienced Manager to oversee the site production, assembly, and facilities operations during the second shift. This role is crucial in ensuring smooth and efficient operations, while maintaining high-quality standards, and fostering a safe and productive work environment. Key Duties and Responsibilities: Operational Oversight : Oversee direction, planning, and execution of site operations (production, assembly, and facilities), while effectively managing key performance indicators. Manage all second shift activities in production, assembly, and facilities. Ensure compliance with safety, quality, and productivity standards. Coordinate with first shift leadership to ensure seamless transition and continuous operations. Team Management : Lead, motivate, and develop second shift staff, fostering a culture of accountability and teamwork. Conduct regular performance evaluations and provide feedback and coaching. Address and resolve personnel issues, including scheduling, attendance, and disciplinary actions. Process and Quality Control : Monitor production and assembly processes to ensure company standards and client specifications are met Implement and maintain quality assurance protocols to minimize defects and rework. Identify and troubleshoot operational issues, implementing corrective actions as needed. Ensure operational compliance with Luminex Quality System including FDA and ISO 13485 requirements as applicable. Ensure effective prioritization, investigation, and resolution of findings impacting Reagent Manufacturing identified through audits, non-conformances, corrective/preventative actions, and customer complaint escalations. Facilities Management : Oversee the maintenance and upkeep of the facility during the second shift. Coordinate with the facilities team to ensure equipment and machinery are in optimal working condition. Address any facilities-related issues promptly to avoid disruptions in operations. Reporting and Documentation : Maintain accurate records of production outputs, staff performance, and any incidents or deviations. Prepare and submit regular reports to senior management on shift performance and any issues. Continuous Improvement : Identify opportunities for process improvements and efficiency gains. Lead or participate in continuous improvement initiatives and projects. Education, Experience, and Qualifications: Bachelor's Degree Business, Operations, Supply Chain, Engineering, Science, or equivalent required with 5+ years or relevant manufacturing operations leadership experience 3+ years of Experience in FDA regulated industry and/or ISO 13485 certified organization Thorough knowledge of ISO 13485:2016 and FDA Quality System requirements Strong knowledge in cleanroom operations Strong knowledge in production automation systems Proven proficiency in promoting safety culture Proficiency in use and optimization of Manufacturing Resource Planning and Manufacturing Execution Systems such as Oracle or SAP Proficiency in the use of Product Lifecycle Management tools, including applied knowledge of Engineering Change Control and BOM construction Applied knowledge of Six Sigma, Lean Manufacturing, and Design for Manufacturability principles Working knowledge of cost accounting/manufacturing finance Proficiency in data analysis tools and technical writing Highly organized with proven time management and prioritization skills Ability to handle the pressure of meeting tight deadlines and adapting to rapidly changing priorities Shift: Position is Tuesday-Friday 2:00pm-12:30am. Please note that in the first 60 days, some training will need to take place on 1st Shift. What We Offer Receive a competitive wages and benefits package as you grow your career at Diasorin. Join our team and discover how your work can impact the lives of people all over the world. Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at or to request an accommodation. The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations. Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations. This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department.
Created: 2024-10-11