Manufacturing Biochemist I

Siemens Healthineers

About The Position

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 CLS Manufacturing Biochemist I. This is a role well suited to an ambitious professional, looking for the next step in their career. As a Manufacturing Biochemist I, you will: Execute, as well as provide expert guidance on SAP transactions/reports, equipment implementation/use, and manufacturing processes. Take part in product release responsibilities, including equipment and software commissioning/validation, review of bill of materials and routings, and product transfer/qualification/validation support. Assist in meeting product demand requirements, driving systemic improvement in manufacturing. This position includes the handling of various types of materials, including hazardous and DEA (Drug Enforcement Agency) controlled materials. This position may suit you well if: You are versed in software applications and comfortable investigating and testing digital and automated solutions to replace manual systems. Experience with SAP and automated manufacturing systems (e.g. MES) is a plus. You have experience in equipment and/or software validation. You have a robust manufacturing process background, a solid understanding of the use and calibration of laboratory equipment during formulation and can demonstrate a strong understanding of GMP in a controlled environment. You have exceptional attention to detail and can provide verification and approval for quality records. The expectation would be to provide leadership and direction, within the department. Identify and initiate continuous improvement activities in line within the Healthineers Performance System (HPS) framework The ability to communicate effectively both written and verbally You have an ability to effectively manage multiple operations in parallel, within defined time ranges. Occasional off-shift work may be required. Required skills to have for the success of this role Associates or Bachelor’s degree in Life Science, Chemistry, or related field of study, or equivalent work experience of >10 years in a related industry or field. Minimum of 5-8 years of manufacturing experience; including experience in a controlled environment Strong mathematical and computer application skills Legible handwriting Must pass a Drug Enforcement Agency (DEA) background check. 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: $79,800 - $109,725 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. To learn more, click here. 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 [email protected]. Please note HR People Connect People Contact Center will not have visibility of your application or interview status. California Privacy Notice: California residents have the right to receive additional notices about their personal information. To learn more, click here. 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.” Data Privacy: We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. We ask instead that you create a profile in our talent community where you can upload your CV. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you an alert when relevant positions become open. Register here to get started. Beware of Job Scams: Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as Siemens Healthineers recruiters/employees. These scammers may attempt to collect your confidential personal or financial information. If you are concerned that an offer of employment with Siemens Healthineers might be a scam or that the recruiter is not legitimate, please verify by searching for the posting on the Siemens Healthineers career site. To all recruitment agencies: Siemens Healthineers does not accept agency resumes. Please do not forward resumes to our jobs alias, employees, or any other company location. Siemens Healthineers is not responsible for any fees related to unsolicited resumes. We are a team of 72,000 highly dedicated employees across more than 70 countries passionately pushing the boundaries of what’s possible in healthcare to help improve people’s lives around the world. As a leader in the industry, we aspire to create better outcomes and experiences for patients no matter where they live or what health issues they are facing. Our portfolio, spanning from in-vitro and in-vivo diagnostics to image-guided therapy and innovative cancer care, is crucial for clinical decision-making and treatment pathways. Our culture: We are part of an incredible community of scientists, clinicians, developers, researchers, professionals, and skilled specialists pushing the boundaries of what’s possible, to improve people’s lives around the world. We embrace a culture of inclusivity in which the power and potential of every individual can be unleashed. We spark ideas that lead to positive impact and continued success.

Requirements

Associates or Bachelor’s degree in Life Science, Chemistry, or related field of study, or equivalent work experience of >10 years in a related industry or field.
Minimum of 5-8 years of manufacturing experience; including experience in a controlled environment
Strong mathematical and computer application skills
Legible handwriting
Must pass a Drug Enforcement Agency (DEA) background check.

Nice To Haves

You are versed in software applications and comfortable investigating and testing digital and automated solutions to replace manual systems. Experience with SAP and automated manufacturing systems (e.g. MES) is a plus.
You have experience in equipment and/or software validation.
You have a robust manufacturing process background, a solid understanding of the use and calibration of laboratory equipment during formulation and can demonstrate a strong understanding of GMP in a controlled environment.
You have exceptional attention to detail and can provide verification and approval for quality records.
The expectation would be to provide leadership and direction, within the department.

Responsibilities

Execute, as well as provide expert guidance on SAP transactions/reports, equipment implementation/use, and manufacturing processes.
Take part in product release responsibilities, including equipment and software commissioning/validation, review of bill of materials and routings, and product transfer/qualification/validation support.
Assist in meeting product demand requirements, driving systemic improvement in manufacturing.
This position includes the handling of various types of materials, including hazardous and DEA (Drug Enforcement Agency) controlled materials.
Identify and initiate continuous improvement activities in line within the Healthineers Performance System (HPS) framework
The ability to communicate effectively both written and verbally
You have an ability to effectively manage multiple operations in parallel, within defined time ranges.
Occasional off-shift work may be required.