Pharmaceutical Lab Technician

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 the global leader shaping the future of PET imaging.

At Siemens Healthineers, we operate the world’s largest PET radiopharmaceutical network — delivering over 1 million doses annually with a >99% fulfillment rate and supporting more than 2,800 imaging centers worldwide.

Important: This is a primarily overnight role. Candidates must be willing to work overnight and have the flexibility to rotate into alternative shifts as business needs evolve.

Why You’ll Love Working Here

• Industry‑leading 5‑week paid training program (in‑person + virtual).
• Competitive benefits: medical/dental/vision, 5% bonus, 100% 401(k) match.
• 20 days PTO + 5 floating holidays.
• Meaningful work that supports patient care and advanced medical imaging.

You are responsible for the synthesis, quality control, packaging, logistics, and strict regulatory compliance of radiopharmaceuticals used in diagnostic imaging and treatment of diseases. Your role supports manufacturing through regular preventive maintenance, calibration, and troubleshooting of analytical equipment used in operations. You also communicate regularly with couriers and customers to ensure the accurate and timely delivery of biomarkers. In addition, you assist with facility housekeeping, maintenance of laboratory inventory levels, creation of quality control documentation as needed, and adherence to strict safety protocols and regulations related to the production and transport of radioactive materials.

Essential Job Functions and Responsibilities

• Operate chemistry instruments (HPLC, GC, TLC, and chemistry modules) and advanced systems (cyclotron) for the routine manufacturing and quality control of radiopharmaceuticals.
• Author and maintain precise documentation for manufacturing, quality control, preventive maintenance, customer support, laboratory investigations, deviations, and out-of-specification events.
• Perform preventive maintenance, inspections, and troubleshooting of critical equipment.
• Prepare products for shipment, coordinate courier logistics, and provide customer support.
• Maintain aseptic environments (cleanroom) to create sterile consumables and prevent contamination during the production of injectable materials.
• Conduct environmental monitoring on a regular and defined basis.
• Maintain compliance with strict safety, sterile environment, and regulatory standards.

Minimum Qualifications

• High school diploma or equivalent required. Specialized skill training or certification may be required.
• Physical Demands: Applicants should be comfortable working in a fast-paced laboratory environment and able to lift up to 100 lbs.
• Willingness to work overtime as needed.
• Detail-oriented with strong critical thinking skills.
• Ability to work independently.
• Basic computer skills such as spreadsheet, word processing, and email.
• Effective verbal and written communication skills.

Preferred Qualifications

• Previous experience in a Pharmacy environment or equivalent
• Understanding of current Good Manufacturing Practices and Good Documentation Practices.
• Previous work experience in a laboratory environment or related role.
• Previous experience with analytical laboratory equipment and laboratory software systems.
• Familiarity with radiation safety or ALARA principles.

Knowledge, Skills, and Abilities

• Excellent communication and interpersonal skills.
• Strong command of Good Documentation Practices (GDP) to ensure data integrity and audit readiness.
• Excellent problem-solving and analytical skills, as well as critical thinking ability.
• Excellent organizational skills and attention to detail.
• Ability to treat confidential information with sensitivity.
• Ability to meet deadlines and work in a fast-paced, multi-priority environment.
• Ability to plan and organize job responsibilities and priorities.
• Ability to apply standard operating procedures (SOPs) in a production environment.
• Demonstrated ability to maintain a sterile environment.
• Ability to understand, prioritize, and implement laboratory safety protocols.

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:

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.

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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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