Technical Writer III

QuidelOrtho • Rochester, NY

2d • $89,000 - $115,000

About The Position

The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most – home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. The Role As we continue to grow as QuidelOrtho, we are seeking a Technical Writer III. The Technical Writer III will manage all aspects of the change process for externally supplied products and components, including timelines to ensure all deliverables associated with the change are completed on time. This position is in Rochester, NY.

Requirements

• Associate Degree and a minimum of 5 years experience.
• Experience with Word / Excel/ Outlook/ Teams.
• Experience with Adobe Professional.
• Windchill Experience.
• FDA Industry Experience.
• Able to communicate in a team environment.
• Excellent communication skills.
• Ability to accomplish tasks with little supervision.
• Self-motivated Team Member.

Nice To Haves

• Bachelors Degree.
• Technical Background.

Responsibilities

• Coordinate with Engineering, relationship/sourcing/business managers, buyer/planners, Regulatory Affairs, Quality, and other functional areas to develop and complete change orders.
• Use detailed knowledge of business systems and processes to shepherd changes through the change control process.
• Use computer skills (Word, Excel, Adobe Acrobat) to revise documents and drawings.
• Complete all changes and related activities to GMP/ISO compliance.
• Assist colleagues with changes, the change process, and document/drawing revisions as needed.
• Interact with suppliers and vendors as needed regarding changes.
• Identify and implement improvements in the change process.

Benefits

• QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time) and paid Holidays.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree