Job Title: Manufacturing Associate III- Redmond WA
Dayshift- Wed-Sat 0700-1800
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 whats possible. Were on a mission to create a place where curiosity isnt just encouragedits celebrated.
Are you someone who asks questions seeks answers and isnt afraid to go deeper #BeCureious with us and see where your curiosity can take you!
The Role: / your challenge in our journey
Were looking for a passionate and curious Manufacturing Associate III to join our team. If youre excited by new challenges solving complex problems and learning every step of the way you might just be the perfect this role youll have the opportunity to drive impactful projects collaborate with bright minds and explore uncharted territories.
As a Manufacturing Associate III at Evotec youll have the freedom to ask the hard questions think outside the box and find creative solutions that push us forward. Its a role where your curiosity will fuel both your personal growth and the success of the team.
Manufacturing Associates III are expected to execute process recipes monitor equipment and processes perform basic tasks including sampling and routine maintenance of lab equipment in support of downstream manufacturing operations. The staff member is expected to comply and follow written procedures for safety requirements cGMP Practices Standard Operating Procedures and manufacturing documentation. Manufacturing Associates III may also assist in media and buffer compounding.
What Youll Do:
Perform and monitor critical processes (i.e. column packing capture and polishing chromatography steps viral inactivation viral filtration and UF/DF operations)
Support the introduction of new products and technologies into the facility
Initiate quality records including but not limited to non-conformances (NC) Corrective/Preventative Actions (CAPA) and assisting in investigations.
Draft and revise Manufacturing Procedures and Standard Operating Procedures as necessary
With minimal supervision set up operate and maintain a majority of MFG equipment; collects data and writes/ updates GMP documentation.
With direction from Floor Lead/ Supervisor propose and test solutions to MFG Operational problems. Be able to identify when a deviation has occurred.
Actively participate in departmental teams NPI. May present run data as applicable.
Train Junior level staff
Respond to equipment alarms with help of Floor Lead.
Effectively communicate with Floor Lead/ Supervisor the status of MFG Operations.
Document operational requirements in batch records in accordance with cGMP and company guidelines
Develop an understanding of equipment and operations used to manufacture biotherapeutics in cGMP manner.
Demonstrate situational leadership within MFG and company responsibilities
Perform other duties as assigned
Who You Are:
Masters degree; or
Bachelors degree and 3 years of Manufacturing & Operations experience; or
Associates degree and 5 years of Manufacturing & Operations experience; or
High school diploma / GED and 7 years of Manufacturing & Operations experience
Preferred Requirements:
Single use technology experience
Capacity to develop solutions to technical issues of moderate scope
Train other personnel on equipment operation
Draft and revise SOPs
Proven knowledge of cGMP requirements to ensure compliance
Experience in operations required for the manufacture of biotherapeutics
Focus on quality and attention to detail
Ability to organize analyze/interpret and effectively communicate data and results
Motivated self-starter with strong mechanical aptitude
Good interpersonal team and communication skills
Troubleshooting skills on Manufacturing equipment including single use equipment
Experience with Delta V/MES
Experience with lab equipment/testing
Be open to change and manage emotions during periods of organizational change.
The base pay range for this position at commencement of employment is expected to be $32.56 to $41.46; Base salary offered may vary depending on the individuals 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.
Required Experience:
IC
Evotec is a global biotechnology company committed to advancing drug discovery & development together with our partners for medicines that matter.