Siemens Healthineers
Technical Writer
– Siemens Healthineers
Join us in pioneering breakthroughs in healthcare. We encourage stepping beyond comfort zones, providing resources and flexibility for professional growth while valuing diversity and individuality.
This full‑time role is within the Package Engineering and Product Labeling organization, focused on developing product labeling for immunoassay and clinical chemistry in vitro diagnostics products. The position collaborates with cross‑functional teams and operates in an agile Scrum framework.
Responsibilities
Create high‑quality instructions and software messaging for laboratory diagnostics professionals, ensuring consistency and compliance with regulatory and company guidelines.
Develop new content and revise existing operator guides, online help, software user interface messages, and other documentation, with a strong focus on content reuse and single‑sourcing.
Collaborate with Product Line Leads, other Technical Writers, SMEs, and engineering teams to produce customer‑facing instructions.
Analyze and interpret engineering and scientific specifications to convey clear customer‑facing information.
Anticipate issues and develop critical solutions proactively.
Work independently within an agile environment, managing documentation in an electronic content management system.
Maintain document control processes (check‑in, check‑out, version control, review, approval, release) in accordance with end‑to‑end document management protocols.
Ensure compliance with Good Documentation Practices and data protection regulations.
Qualifications
Excellent English writing skills with an understanding of localization and proven technical writing experience in Life Sciences, Software, or a similar industry.
Strong technical writing skills and familiarity with XML content management (preferred) or other authoring tools such as Adobe FrameMaker or InDesign.
Experience with XML‑based content management systems and intermediate proficiency in Adobe FrameMaker.
Knowledge of medical device regulations and international standards (preferred).
Experience in engineering, software, or medical technology is a plus.
Highly organized, able to prioritize tasks, and collaborate effectively in a virtual environment.
Education
Technical Writing Certification (preferred) or equivalent.
Bachelor’s degree in technical writing, business, science, engineering, software, or related field.
Experience
Minimum 5 years of direct technical writing experience in a medical device manufacturing company or similar.
Expert skill level using current versions of standard authoring tools.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Marketing, Public Relations, and Writing/Editing
Industries Hospitals and Health Care
Locations Oak Ridge, TN • 1 day ago Knoxville, TN • 1 day ago
Base Pay Range Min $87,620 – Max $131,440
Benefits Medical, dental, vision insurance; 401(k); 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… (the full EEO statement continues with details about race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, disability, parity, military status, etc.). All qualified applicants will receive consideration for employment without regard to any protected category.
EEO is the Law Applicants and employees are protected under Federal law from discrimination. To learn more, view the EEO policy.
Reasonable Accommodations Siemens Healthineers is committed to equal employment opportunity. Persons with disabilities will be provided reasonable accommodations in the application and selection process. Contact the HR People Connect People Contact Center for support.
California Privacy Notice California residents have the right to receive additional notices about their personal information. To learn more, view the privacy notice.
Export Control Successful candidates must comply with U.S. export control law, including the Export Administration Regulations (EAR), International Traffic in Arms Regulations (ITAR), and other relevant regulations. Siemens Healthineers follows U.S. export control laws and regulations.
Data Privacy We take data privacy seriously and comply with GDPR and related legislation. Resumes should be submitted via the talent community profile, not by email.
Beware of Job Scams Be cautious of fraudulent job postings or recruiters. Verify postings on the Siemens Healthineers career site.
Recruitment Agencies Siemens Healthineers does not accept agency resumes. Do not forward resumes to our jobs alias or employees. Siemens Healthineers is not responsible for unsolicited resume fees.
#J-18808-Ljbffr
– Siemens Healthineers
Join us in pioneering breakthroughs in healthcare. We encourage stepping beyond comfort zones, providing resources and flexibility for professional growth while valuing diversity and individuality.
This full‑time role is within the Package Engineering and Product Labeling organization, focused on developing product labeling for immunoassay and clinical chemistry in vitro diagnostics products. The position collaborates with cross‑functional teams and operates in an agile Scrum framework.
Responsibilities
Create high‑quality instructions and software messaging for laboratory diagnostics professionals, ensuring consistency and compliance with regulatory and company guidelines.
Develop new content and revise existing operator guides, online help, software user interface messages, and other documentation, with a strong focus on content reuse and single‑sourcing.
Collaborate with Product Line Leads, other Technical Writers, SMEs, and engineering teams to produce customer‑facing instructions.
Analyze and interpret engineering and scientific specifications to convey clear customer‑facing information.
Anticipate issues and develop critical solutions proactively.
Work independently within an agile environment, managing documentation in an electronic content management system.
Maintain document control processes (check‑in, check‑out, version control, review, approval, release) in accordance with end‑to‑end document management protocols.
Ensure compliance with Good Documentation Practices and data protection regulations.
Qualifications
Excellent English writing skills with an understanding of localization and proven technical writing experience in Life Sciences, Software, or a similar industry.
Strong technical writing skills and familiarity with XML content management (preferred) or other authoring tools such as Adobe FrameMaker or InDesign.
Experience with XML‑based content management systems and intermediate proficiency in Adobe FrameMaker.
Knowledge of medical device regulations and international standards (preferred).
Experience in engineering, software, or medical technology is a plus.
Highly organized, able to prioritize tasks, and collaborate effectively in a virtual environment.
Education
Technical Writing Certification (preferred) or equivalent.
Bachelor’s degree in technical writing, business, science, engineering, software, or related field.
Experience
Minimum 5 years of direct technical writing experience in a medical device manufacturing company or similar.
Expert skill level using current versions of standard authoring tools.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Marketing, Public Relations, and Writing/Editing
Industries Hospitals and Health Care
Locations Oak Ridge, TN • 1 day ago Knoxville, TN • 1 day ago
Base Pay Range Min $87,620 – Max $131,440
Benefits Medical, dental, vision insurance; 401(k); 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… (the full EEO statement continues with details about race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, disability, parity, military status, etc.). All qualified applicants will receive consideration for employment without regard to any protected category.
EEO is the Law Applicants and employees are protected under Federal law from discrimination. To learn more, view the EEO policy.
Reasonable Accommodations Siemens Healthineers is committed to equal employment opportunity. Persons with disabilities will be provided reasonable accommodations in the application and selection process. Contact the HR People Connect People Contact Center for support.
California Privacy Notice California residents have the right to receive additional notices about their personal information. To learn more, view the privacy notice.
Export Control Successful candidates must comply with U.S. export control law, including the Export Administration Regulations (EAR), International Traffic in Arms Regulations (ITAR), and other relevant regulations. Siemens Healthineers follows U.S. export control laws and regulations.
Data Privacy We take data privacy seriously and comply with GDPR and related legislation. Resumes should be submitted via the talent community profile, not by email.
Beware of Job Scams Be cautious of fraudulent job postings or recruiters. Verify postings on the Siemens Healthineers career site.
Recruitment Agencies Siemens Healthineers does not accept agency resumes. Do not forward resumes to our jobs alias or employees. Siemens Healthineers is not responsible for unsolicited resume fees.
#J-18808-Ljbffr