Senior Director, Manufacturing Operations - Site Based, Redmond, WA

Evotec; Redmond; On-site; AUD 272,000 - 322,000; Full time

Benefits offered by this job

Growth opportunities

Flexible on-site work

Inclusive culture

Cutting-edge projects

Big ideas culture

Job summary

Evotec is seeking a Senior Manufacturing Leader to oversee a team performing late-stage clinical and commercial biologics manufacturing, including cell culture, purification, and media preparation. This role requires strong on-the-floor presence, leadership, and adherence to cGMP in daily operations.

Candidates should have deep expertise in disposable-based manufacturing technologies and participate in commissioning, validation, and regulatory support activities while mentoring staff and

Qualifications

• Bachelor’s degree in biological or engineering science and 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.

Responsibilities

• Lead a group of manufacturing staff in late-stage biologics operations.
• Ensure on-the-floor execution and cGMP compliance in day-to-day activities.
• Troubleshoot and provide technical expertise; support commissioning and validation activities.
• Maintain staff training compliance and write/adhere to procedures.

Skills

Cell culture operations

Purification operations

Solution preparation

Staff leadership

cGMP compliance

Technical troubleshooting

Equipment knowledge

Quality focus

Time management

Interpersonal communication

Education

Bachelor’s degree in biological or engineering science

Tools

DeltaV process automation

BAS systems

Job description

About Us: this is who we are

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.

Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? Be Curious with us and see where your curiosity can take you!

The Role: / your challenge, …in our journey

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. Additional job responsibilities may include troubleshooting and/or providing technical expertise, finite scheduling, ensuring staff training compliance, executing against approved written procedures, participating in commissioning and validation activities, maintaining required cGMP compliant systems, and providing support for regulatory and site inspections.

Education And Qualification 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
• Candidate must possess strong focus on quality and attention to detail
• Possess effective task/time management organizational skills
• Motivated, self-starter with strong mechanical aptitude
• Good interpersonal, team, and communication skills are a must Excellent oral and written communication skills

Additional 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.

Why Join Us

• 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.
• Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. This is a site based role.
• 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.
• A Place for Big Ideas: We don’t just talk about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them.

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. Additional total rewards include 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, generous paid time off and paid holiday, wellness and transportation benefits.

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.