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/antigensMaintaining cGMP compliance and adherences to site SOP’sSupporting and providing technical guidance to employees  Driving improvements in manufacturing processesDeveloping/coaching employeesAuditing manufacturing documentation including but not limited to  Manufacturing Batch Records, Bills of Materials, Routings, Process Documents, and SOP’sWorking with Biochemists to coordinate and monitor day to day assignments of the groupSupport training/training development of manufacturing processesReviewing 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 appropriateAuthoring, 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 demandsFostering 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 industryStrong 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 leadershipMust pass a Drug Enforcement Agency (DEA) background check.

Preferred Knowledge/Skills, Education, and Experience

Experience with AKTAsA solid technical background in manufacturing processesA background with program development/modificationExperience working with automated manufacturing equipment. Prior experience manufacturing commercialized automated immunoassays and/or ELISA and chemiluminescent productsWorking knowledge of Lean and other Continuous Improvement philosophies and techniquesProficiency with Microsoft Office applicationsPrior knowledge and use of SAP or similar MRP/ERP systemExperience in presenting data in table and graphic charts in Excel.

Who we are: We are a team of more than 73,000 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 annual base pay for this position is:

Min $93,000 - Max $139,500

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 Law: Applicants and employees are protected under Federal law from discrimination.

Reasonable Accommodations: Siemens Healthineers is committed to equal employment opportunity. As part of this commitment, we will ensure that persons with disabilities are provided reasonable accommodations.

If you require a reasonable accommodation in completing a job application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form here. If you’re unable to complete the form, you can reach out to our HR People Connect People Contact Center for support at peopleconnectvendorsnam.func@siemens-healthineers.com. Please note HR People Connect People Contact Center will not have visibility of your application or interview status.

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Export Control: “A successful candidate must be able to work with controlled technology in accordance with US export control law.” “It is Siemens Healthineers’ policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.”

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