Biochemist 1

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.

This Biochemist I position impacts people’s health, and well-being all around the world, while working on a new and exciting automation platform; the Siemens Atellica. Position supports Manufacturing personnel via technical expertise and guidance, as they build/test diagnostic reagents and materials that will be used by clinical labs on Atellica, Centaur, and Centaur CP automation platforms. Position reports to Manager of Technical Operations within the Manufacturing sector.  Assay portfolio focus includes Hepatitis and Allergy although work on additional assays/portfolios may be required.

This position includes the handling of all types of materials, including hazardous and DEA (Drug Enforcement Agency) controlled materials.

This is a role well suited to an ambitious professional looking for the next step in their career. As a Biochemist 1, you will be responsible for:

• Leading projects throughout the project life cycle
• Coordinating with other departments and Siemens Healthineers sites in support of product design and process changes
• Coordinating and carrying out root cause investigations and implementing corrective and preventive actions (CAPA)
• Create and participate in the design of experiments (DOE) as part of validation and verification activities
• Writing compliance documentation associated with technical investigations, data analyses, and experimental conclusions
• Working in the laboratory running Atellica, Centaur, and CP instrumentation with serum and other biological fluids of human and animal origin

Required Knowledge/Skills, Education, and Experience

• BS in Medical Technology, Biology, Chemistry, Biochemistry
• 1 + years job related experience
• Experience working on CAPA investigations and implementations
• Experience working on design and/or process change projects
• Strong work ethic, excellent written and communication skills
• Must be flexible and demonstrate the ability to switch priorities to meet business needs
• Proficiency with Microsoft Office

Qualified Applicants must be legally authorized for employment in the United States.

At Siemens Healthineers, we value those who dedicate their energy and passion to a greater cause. Our people make us unique as an employer in the med-tech industry. What unites and motivates our global team is the inspiration of our common purpose:  To innovate for healthcare, building on our remarkable legacy of pioneering ideas that translate into even better healthcare products and services. We recognize that taking ownership of our work allows both us and the company to grow. We offer you a flexible and dynamic environment and the space to move beyond your comfort zone to grow both personally and professionally. 

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:

$82,150 - $112,959

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.

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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.

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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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