Chromatography Senior Supervisor

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. The Chromatography Manufacturing (Antibody Purification, Biotinylated Conjugates, and Lite Reagent Concentrates) Senior Supervisor position supervises 13 direct reports, manages weekend coverage of the work center, maintains cGMP compliance and adherence to site SOP's, works cross-functionally, and represents Chromatography Manufacturing in cross-functional team meetings. This position includes the handling of all types of materials, including biohazardous, hazardous, and DEA (Drug Enforcement Agency) controlled materials. A Chromatography Manufacturing Senior Supervisor is responsible for : Supervising Chromatography Operators, Technicians, and Biochemists. Purification, conjugation, and labeling of antibodies/antigens Maintaining cGMP compliance and adherences to site SOP's Supporting and providing technical guidance to employees Driving improvements in manufacturing processes Developing/coaching employees Auditing manufacturing documentation including but not limited to Manufacturing Batch Records, Bills of Materials, Routings, Process Documents, and SOP's Working with Biochemists to coordinate and monitor day to day assignments of the group Support training/training development of manufacturing processes Reviewing and approving employee Timecards and PTO requests to ensure adequate staffing to meet scheduled demands. Representing Chromatography Manufacturing in cross functional meetings including but not limited to element teams, planning and scheduling, and product troubleshooting. Supporting and implementing Change Control Projects as appropriate Authoring, Reviewing, and Approving Quality System documentation including but not limited to Quality Notifications (QN's), Temporary Manufacturing Deviations (TMDs). Corrective and Preventive Actions (CAPA's), and Change Impact Assessment (CIA's) Providing training to employees for quality system documentation Back-filling on the manufacturing floor to meet work center demands Fostering a diverse and inclusive environment as part of world class team Required Knowledge/Skills, Education, and Experience Bachelor's Degree in Life Science discipline. (Biology, Chemistry, Engineering, or other applicable Science Degree) 3-5 years chromatography work experience. 5-7 years' experience working in a similar supervisory or leadership role in the medical diagnostic/ medical device industry Strong understanding of cGMP manufacturing in a controlled environment, as well as an understanding of ISO requirements. Solid understanding of the use of laboratory equipment used in manufacturing and witnessing manufacturing batch records. Experience executing troubleshooting and investigation work, as well as associated outcomes. Effective communication skills, both verbal and in written form. The ability to communicate is critical to the successful delivery of information to customers and the team, with regards to priorities and expectations. Excellent time management skills Ability to meet multiple commitments, for both the daily manufacturing deliverables, as well as the mid to long term projects. Ability to present information in technical or scientific writing format. Ability to provide guidance and leadership Must pass a Drug Enforcement Agency (DEA) background check. Preferred Knowledge/Skills, Education, and Experience Experience with AKTAs A solid technical background in manufacturing processes A background with program development/modification Experience working with automated manufacturing equipment. Prior experience manufacturing commercialized automated immunoassays and/or ELISA and chemiluminescent products Working knowledge of Lean and other Continuous Improvement philosophies and techniques Proficiency with Microsoft Office applications Prior knowledge and use of SAP or similar MRP/ERP system Experience in presenting data in table and graphic charts in Excel. Who we are : We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.

How we work:

When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual's potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world's most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably. To find out more about Siemens Healthineers businesses, please visit our company page here . The base pay range for this position is: $95,770 - $131,681 Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance. The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan. life insurance, long-term and short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time.

Equal Employment Opportunity Statement:

Siemens Healthineers is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law. EEO is the

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