Senior Technical Writer – Medical Devices

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

     

JOB DESCRIPTION:

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:

• Career development with an international company where you can grow the career you dream of.
• Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
• An excellent retirement savings plan with high employer contribution
• Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks.

The Opportunity

We currently have an opportunity for a Senior Technical Writer to join our Abbott Medical Device team.  This individual researches, writes, and edits User Manuals to support new and sustaining projects as well as collaborate with project teams to gather information for User Manuals. Additionally, will work with Technical Publications peers to follow internal processes and procedures and understand and comply with medical device regulatory requirements related to labeling (User Manuals).

What You’ll Work On

• Working within the confines of the Abbott Quality Assurance policy as well as domestic and international regulatory requirements, writes, edits, and formats a wide variety of assigned product manuals.
• Collaborates with development engineering, marketing, regulatory affairs, and clinical engineering personnel, among others, to ensure accuracy and completeness. 
• Recommends overall organization and layout, mode of presentation, publication methods, and related matters. 
• Develops publication concepts for the best communication of subject matter. 
• Coordinates with graphic design, translation, and production personnel to meet publication schedules.  Coordinates publication with outside sources and vendors.
• Leads projects to implement new technology for use by Technical Publications.
• Leads projects to improve departmental processes that require cooperation from other functional groups.
• Troubleshoots existing processes and technologies. 
• Remains current on developments in and knowledge of the company's products, markets, policies, and objectives, including regulatory requirements and restrictions.
• Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
• Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.  Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

Required Qualifications

• Bachelor’s Degree in Science, Medical Technology or a relevant technical discipline OR an equivalent combination of education and experience
• Minimum 3 years relevant experience in a related area such as R&D, T