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. Join our team now at Siemens Healthineers as a Biochemist I - Standards Lab - Weekend Coverage. Tuesday- Saturday shift The Biochemist I - Standards position plays a key role for the Standards Manufacturing team at the Siemens East Walpole facility. This position will cover Laboratory Diagnostic Manufacturing in the Standards and Controls Manufacturing Work Center. This role will provide weekend coverage, Tuesday - Saturday with training occurring on Monday - Friday. Reporting to the Senior Manager of Manufacturing-Bulk Formulation, the primary functions of the Biochemist I position are to; Formulate, Tests, and Release, all Control System materials for Centaur and Atellica assays produced in Walpole Manufacturing Facility, maintain cGMP compliance and adherence to site SOP's, provide technical guidance to Manufacturing Technicians, and to represent Standards Manufacturing as a Subject Matter Expert (SME) in cross-functional team meetings. This position includes the handling of all types of materials, including hazardous and DEA (Drug Enforcement Agency) controlled materials. The successful candidate must pass a DEA background check. Your role: * You will manufacture Siemens Control System materials using established Manufacturing protocols and procedures * You will run and interpret In-Process testing on Control System materials using established Quality Control protocols and procedures. * You will demonstrate proficiency in running and maintaining Testing Equipment within the Standards Manufacturing Lab. * You will audit manufacturing documentation including Manufacturing Batch Records, Bills of Materials, Routings, Process Documents and SOP's * You will help provide training to qualify technicians for manufacturing activities * You will Identify and initiate continuous improvement activities in line within the Healthineers Performance System (HPS) framework * You will represent Standards Manufacturing in cross functional meetings including design element teams, planning and scheduling, and product troubleshooting projects May be asked to temporarily assume Biochemist II responsibilities on a limited basis with direct support from Senior Manager of Manufacturing Your expertise: * BS/BA in related discipline, or advanced degree, where required, or equivalent combination of education and experience * 1-3 years' experience working in a similar role in the medical diagnostic/ medical device industry * Solid working knowledge of cGMP requirements * Excellent organization and time management skills * Excellent laboratory technique * High attention to detail and commitment to accuracy * Excellent communication skills both verbal and written * Ability to lift up to 50 pounds * Prior experience manufacturing commercialized automated immunoassays and/or ELISA and chemiluminescent products * Proficiency with Microsoft Office applications * Prior knowledge and use of SAP or similar MRP/ERP system Who we are: We are a team of more than 71,000 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. 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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. 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 by clicking on this link Accommodation for disability form If you're unable to complete the form, you can reach out to our AskHR team for support at 1-866-743-6367. 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