Manufacturing Manager - Nights, Site Based, Redmond, WA

Evotec SE; Redmond (WA); On-site; USD 100,000 - 150,000; Full time

Benefits offered by this job

Medical, Dental, Vision

401(k) matching

Paid time off

Job summary

Evotec SE in Redmond, WA is seeking a Manager of Manufacturing Operations - Purification to supervise a 24/7 shift and provide technical leadership on purification processes for biotherapeutics.

The role requires strong cGMP knowledge, hands-on floor presence, and collaboration with cross-functional teams to ensure quality, documentation, and successful start-up, validation, and technology transfer activities.

Qualifications

• Knowledge of cGMP requirements to ensure compliance.
• Significant experience in purification operations required for the manufacture of biotherapeutics.
• Strong focus on quality and attention to detail.
• Excellent communication with senior leadership.
• Ability to organize, analyze data and communicate results.
• Motivated, self-starter with strong mechanical aptitude.
• Good interpersonal, team, and communication skills are a must.
• May lead cross-functional teams within and external to Just.
• Responds to equipment alarms.
• Excellent oral and written communication skills.

Responsibilities

• Supervise a shift to cover 24/7 operation.
• Generate and maintain cGMP manufacturing and technical documentation.
• Troubleshoot and provide technical expertise for investigations.
• Ensure staff training and compliance with cGMP.
• Execute plant start-up, commissioning and validation activities.
• Support technology and process transfer; assist capital budgeting.
• Respond to equipment alarms and lead cross-functional projects.

Skills

cGMP knowledge

Purification operations

Quality focus

Technical troubleshooting

Cross-functional leadership

Data interpretation

Effective communication

Education

Master’s degree + 3 years experience

Bachelor’s degree + 5 years experience

Tools

DeltaV

Job description

Manager, Manufacturing Operations - Purification | Redmond, WA

This position will responsible for supervising a shift to cover 24/7 operation and requires significant on-the-floor presence, as well as technical subject matter expertise in purification operations. Additional job responsibilities will include generation and maintenance of cGMP manufacturing and technical documentation, troubleshooting and/or providing technical expertise to perform troubleshooting efforts or lead investigations, ensuring staff training and compliance, execution of plant start-up commissioning and validation activities, and implement and maintain required cGMP compliant systems. The manager may also participate in finite scheduling, aspects of technology and/or process transfer, identify process gaps and technology issues, determine solutions and remediation plans, provide support for regulatory and site inspections, and provide input to department capital and expense budgets.

Educational Requirements:

• Master’s degree and 3 years of Manufacturing or Operations experience; or
• Bachelor’s degree and 5 years of Manufacturing or Operations experience

Qualification Requirements:

• Knowledge of cGMP requirements to ensure compliance
• Significant experience in purification operations required for the manufacture of biotherapeutics
• Candidate must possess strong focus on quality and attention to detail
• Execute downstream technology strategies from bioreactor recovery, chromatography column purification, impurity removal, viral inactivation and filtration, UF/DF, and sterile filtration
• Excellent communication with senior leadership
• Possess effective task/time management organizational skills
• Capacity to develop solutions to technical issues of moderate scope
• Ability to organize, analyze/interpret, and effectively communicate data and results
• Motivated, self-starter with strong mechanical aptitude
• Good interpersonal, team, and communication skills are a must
• May lead cross-functional teams within and external to Just. May be a core department lead in NPI.
• Responds to equipment alarms.
• Excellent oral and written communication skills

Additional Preferred Qualifications:

• Proven record of accomplishment managing, supervising and developing staff
• In-depth knowledge of purification equipment, operations, and engineering principles
• Recognized technical mastery of disposable manufacturing technologies at commercial scale
• Participation in client and regulatory agency audits
• Uses technical depth and breadth to develop solutions to deviation investigations, leads CAPA projects, or coordinates more in depth troubleshooting issues where vendors may be involved.
• Fundamental understanding and basic operation of process automation (DeltaV)
• Experienced in technology and/or process transfer for late stage clinical manufacturing or commercial qualification campaigns; commercial campaign support
• Application of knowledge and expertise to solve complex technical problems; may apply novel approach that provides significant technology advancement
• Active participation/lead technical projects with collaborators and vendors
• Experience with finite scheduling tools and allocation of resources and equipment

The base pay range for this position at commencement of employment is expected to be $100,000 to $150,000; Base salary offered may vary depending on 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.