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Evotec

Quality Risk Manager, QTR - site based, Redmond, WA

Evotec, Redmond, Washington, United States, 98052

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Overview

Quality Risk Manager, QTR - site based, Redmond, WA — Evotec Job Title: Quality Risk Manager, QTR Location: Redmond, WA with travel to Seattle, WA site Shifts: Days, Monday to Friday Department: Quality Reports To: Sr. Manager QEV At Just Evotec Biologics, we believe that curiosity is the spark that drives innovation and success. We’re a forward-thinking team that challenges the status quo, learns from each other, and pushes the boundaries of what’s possible. We’re on a mission to create a place where curiosity is celebrated. The Site Quality Risk Manager (Redmond/Seattle) provides quality oversight of the Seattle and Redmond Risk program, ensuring compliance with the Just Pharmaceutical Quality System (PQS) and regulations. This role partners to build, guide, facilitate and develop solutions to identify and reduce risks at the site level. The Site Quality Risk Manager, Redmond and Seattle sites, reports to the Sr. Manager of the Quality Technical and Risk (QTR) department.

What You’ll Do Facilitate and coordinate formal Risk Assessments with cross functional groups to identify risks.

Work with process owners and subject matter experts to identify required mitigations and drive risk down to acceptable levels.

Manage the site risk register for both the Seattle and Redmond facilities.

Communicate major risks and associated mitigation plans to senior management.

Continue the development and improvement of Just-Evotec Risk Management program.

Mentor and train functional groups in the area of Risk Management to increase risk intelligence within the broader organization.

Partner with internal/external collaborators, vendors, and regulatory agencies to anticipate and resolve risk and maintain GxP compliance.

This position is field based and requires onsite support at Redmond or the Seattle facility depending on site needs.

Who You Are A curious problem-solver with a passion for learning and growing in a dynamic environment.

Aim to continuously improve, adapt, and innovate.

Natural collaborator who loves sharing ideas and learning from others.

Comfortable with ambiguity and thrives in environments that encourage curiosity and experimentation.

Excellent communicator, both verbally and in writing.

Self-starter who takes initiative and owns projects.

Bachelor’s degree in biological sciences, chemistry, biochemistry, engineering, computer science or related life science field.

4+ years of relevant experience in Risk Management; experience in biopharmaceutical cGMP manufacturing preferred.

Ability to work independently and in teams; strong problem-solving, partner/customer focus, and ability to work with complex systems.

Knowledge of Risk Management, Data Integrity, Industry guidelines, US & EU regulatory requirements.

Knowledge of risk analysis methodologies and tools (e.g., HACCP, HAZOP, FMEA, RRF).

Why Join Us Growth Opportunities: ongoing learning, mentorship, and new projects.

Flexible Work Environment: onsite role with flexible work options to balance life and work.

Inclusive Culture: diverse and inclusive environment where curiosity is valued.

Innovative Projects: work on groundbreaking initiatives and cutting-edge technology.

A Place for Big Ideas: we welcome new ideas and outside-the-box thinking.

Note: Base pay range at commencement of employment is expected to be $92,400 to $126,500, with potential discretionary bonuses and comprehensive benefits including medical, dental, vision, disability, life insurance, 401k match, PTO, holidays, wellness, and transportation benefits. Sponsorships are not available for this role. Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

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