Medical Writer Job at Abbott – Build a Career in Clinical Evaluation Reporting
If you are searching for a rewarding medical writer job in the medical device industry, Abbott offers an excellent opportunity to work on Clinical Evaluation Reporting (CER) for innovative healthcare technologies. This role is ideal for professionals seeking long-term growth through Abbott careers, while contributing to high-impact healthcare jobs that improve lives globally.
Job Details:
- Position: Medical Writer II / Clinical Evaluation Reporting (CER) – Medical Devices
- Location:
- Maple Grove, MN
- Plano, TX
- Sylmar, CA
- Atlanta, GA
- Santa Clara, CA
About the Company:
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Its portfolio of life-changing technologies spans diagnostics, medical devices, nutritionals, and branded generic medicines. With more than 114,000 employees serving people in over 160 countries, Abbott is widely recognized among top employers offering impactful healthcare jobs.
Qualifications:
- Bachelor’s degree in Medical Technology or equivalent experience
- Minimum 2 years of relevant professional experience in medical writing, regulatory affairs, clinical research, quality, or R&D
- Strong written and verbal communication skills
- Excellent organizational skills with strong attention to detail
- Ability to manage multiple projects and meet deadlines
Preferred:
- Advanced degree in medicine or related discipline
- 1–4 years of medical writing experience, including CER writing
- Experience in experimental design and data interpretation
- Knowledge of medical devices, quality systems, and regulatory frameworks
- Proficiency in MS Word, Excel, PowerPoint, and Outlook
- Ability to work in a matrixed and fast-paced global environment
Medical Writer Job Description:
In this medical writer job, the professional authors and contribute to Clinical Evaluation Plans and Reports (CEP/CER), SSCPs, regulatory responses, and related documentation. The role involves evaluating and summarizing clinical evidence from literature, clinical investigations, post-market surveillance, and risk management sources.
Collaboration across Regulatory Affairs, Quality Engineering, Clinical Affairs, Medical Affairs, and other teams is a core part of this role within Abbott careers.
Medical Writer Job – Key Responsibilities:
- Write and contribute to Clinical Evaluation Reports, Plans, SSCPs, and regulatory responses
- Evaluate and analyze clinical evidence from multiple data sources
- Support regulatory submissions and responses to notified bodies
- Review IFUs, patient guides, risk management files, and clinical protocols
- Collaborate with cross-functional teams across regulatory, clinical, quality, and engineering functions
- Ensure compliance with ISO, MDR, FDA, and Abbott SOPs
- Maintain high standards of quality, accuracy, and data integrity
