Laboratory Technician-3

Siemens Healthineers AG; Schönhausen (Elbe); Vor Ort; EUR 50.000 - 68.000; Vollzeit

Benefits dieser Stelle

Medical insurance

Dental insurance

Vision insurance

401(k) retirement plan

Life insurance

Long-term disability insurance

Short-term disability insurance

Paid parking/public transportation

Paid time off

Paid sick and safe time

Zusammenfassung

Siemens Healthineers AG is seeking an R&D Lab Technician to join our Interventional Oncology (IO) development team, working on embolics and implantable microsphere devices. You will assist with testing, analysis, process development, and lab management to support new and existing products.

The ideal candidate holds an Associate or 4-year degree and at least 2 years in a regulated lab, with experience in microscopy, FTIR, HPLC, and microsphere analysis; familiarity with FDA/QSR and ISO 13485 is

Qualifikationen

• Associate or 4-year degree preferred in biology, chemistry, or physics.
• 2+ years of laboratory experience in a medical device or regulated industry preferred.
• Knowledge of techniques such as microscopy, FTIR, HPLC, and microsphere analysis preferred.
• Experience with laboratory equipment management is preferred.
• Familiarity with FDA/Regulatory and ISO quality issues is preferred.

Aufgaben

• Apply basic scientific principles and laboratory procedures to test method execution.
• Operate laboratory instruments, observe, calculate, and record results.
• Characterize microsphere-based devices for structural and chemical properties.
• QA testing of implantable devices to ensure design conformance.
• Plan and conduct R&D activities for implantable microsphere devices.
• Assist in development of prototype implantable devices to demonstrate feasibility.
• Contribute to new product development and cost-reduction activities.
• Write technical documentation including process descriptions and test methods.
• Manage laboratory equipment, tools, and materials.
• Coordinate installation of new laboratory equipment with vendors and per Varian quality requirements.
• Contribute to DHF maintenance and FDA/ISO quality compliance.
• Execute process improvements related to FDA 510(k), QSR and ISO 13485.
• Participate in complaint investigations and failure analysis.
• Provide root cause analysis and drive CAPA implementation.
• Perform other duties as assigned.

Kenntnisse

Microscopy

FTIR

HPLC

Microsphere analysis

Lab equipment management

Lab software

Regulatory awareness

Ausbildung

Associate or 4-year degree in biology/chemistry/physics

Tools

Laboratory software

Jobbeschreibung

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.

Siemens Healthineers is seeking an R&D Lab Technician to join our Interventional Oncology (IO) development team. The individual will be a member of our growing embolics team that is focused on treating cancers by delivery internal chemical/radiation therapy and occluding the blood supply to tumors. The individual would contribute by assisting with testing, analysis, process development, equipment management, and lab management related to new and existing microsphere products. The ideal candidate would be a self-driven individual with a passion for implantable therapies and a desire to work on products that change people’s lives.

Responsibilities

• Apply basic scientific principles and laboratory procedures to test method execution

• Operate laboratory instruments, make observations, calculate, and record results

• Characterize microsphere-based devices for structural and chemical properties

• Quality assurance testing of implantable devices to ensure conformance to design specifications

• Plan and conduct R&D activities to define and develop implantable microsphere devices, including test execution and basic research

• Assist in development of prototype implantable devices to demonstrate technical feasibility

• Assist in new product development projects and cost-reduction design activities

• Write technical documentation including process descriptions and test methods

• Manage laboratory equipment, tools, and materials

• Manage installation of new laboratory equipment with vendors and through Varian quality requirements

• Contribute to and maintain FDA compliant Design History Files (DHF)

• Execute process improvements as they relate to quality system compliance with FDA 510(k), QSR and ISO 13485

• Participate in complaint investigations, and failure analysis of products

• Provide root cause analysis support and drive the implementation of corrective action for process-related issues

• Performs other duties as assigned or required

Qualifications & Experience

• Associate or 4-year degree preferred in biology, chemistry, or physics

• 2+ years of laboratory experience with preference for experience in medical device or other regulated industry

• Equivalent combinations of education and experience may be considered

• Knowledge of laboratory techniques such as microscopy, FTIR, HPLC, and general chemical and microsphere analysis methods is preferred

• Experience with laboratory equipment management is preferred

• Experience with laboratory software is preferred

• Familiarity with the medical device Regulatory (FDA & MDD) and Quality (QSR & ISO 13485) issues or similarly regulated industry is preferred

• Experience working within a company’s Quality System is preferred

• Experience in the development of regulatedmedical devicesor combination products is preferred

• Experience with design verification & validation is preferred

• Able to define and develop test procedures and to perform design verification

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:

$56,550 - $77,759

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 Aff… 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 [e-mail]. 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.”