Senior Director, Manufacturing Operations - Site Based, Redmond, WA
About Us
At Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what’s possible. We're on a mission to create a place where curiosity isn't just encouraged—it’s celebrated.
About the Role
The focus of this job is to lead a group of manufacturing staff in the execution of late-stage clinical and commercial biologics manufacturing operations, including cell culture, purification, and media/solutions preparation. This position requires significant on-the-floor presence and leadership, focused specifically on day-to-day operations using disposable-based manufacturing technologies and ensuring cGMP compliance.
- Troubleshoot and/or provide technical expertise
- Finite scheduling
- Ensure staff training compliance
- Execute against approved written procedures
- Participate in commissioning and validation activities
- Maintain required cGMP compliant systems
- Provide support for regulatory and site inspections
Requirements
- Bachelor’s degree in biological or engineering science
- 15+ years relevant experience
- Technical mastery of cell culture, purification, and solution preparation operations using disposable-based manufacturing technologies
- Proven knowledge of cGMP requirements to ensure compliance
- Previous experience managing the activities of both individuals and large groups of staff
- In-depth knowledge of equipment, operations, and engineering principles
- Strong focus on quality and attention to detail
- Effective task/time management and organizational skills
- Motivated, self-starter with strong mechanical aptitude
- Good interpersonal, team, and communication skills
- Excellent oral and written communication skills
Preferred Qualifications
- Strong understanding of process automation (e.g. DeltaV) and BAS systems
- Commissioning and validation experience, including risk assessments, user requirement specifications, execution of DQ, IQ, OQ, and PQ activities, and validation summary reports
- Applies knowledge and expertise to solve complex technical problems
- Significant contributor to multi-disciplinary teams at the functional level
- Mentors and provides technical advice to individuals within the team
- Thorough working knowledge of US FDA CFRs and European EMA, including ICH regulations
Benefits
- Discretionary annual bonus
- Comprehensive benefits to include Medical, Dental, and Vision
- Short-term and long-term disability
- Company paid basic life insurance
- 401k company match
- Flexible work options (this is a site-based role)
- Generous paid time off and paid holidays
- Wellness and transportation benefits
Growth Opportunities: We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow.
Inclusive Culture: We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.
Innovative Projects: You’ll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.
Pay
The base pay range for this exempt, salaried position at commencement of employment is expected to be $190,000 to $225,000. Base salary offered may vary depending on the individual’s skills, experience, and competitive market value.