Senior AutomationProcess Controls Engineer – Manufacturing Process Automation Redmond site based
Senior AutomationProcess Controls Engineer – Manufacturing Process Automation Redmond site based
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Job Description
Job Title: Senior Automation/Process Controls Engineer
About Us: this is who we are
At Just Evotec Biologics 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
This role is part of the Automation team in Global MSAT that is responsible for defining the automation (DeltaV) standards for the Manufacturing platform and ensuring alignment across the network as well as provide automation support to Just-Evotecs manufacturing sites. This includes designing and implementing creative solutions to complex technical challenges in helping Just achieve a novel flexible and reconfigurable cGMP manufacturing facility focused on continuous processing. The role will have an advanced proficiency of DeltaV process control automation (SCADA and DCS) used for bioprocessing control as well as at least some experience in other automation platforms (ie Siemens Allen-Bradley Wonderware etc.). Experience working in a GMP environment change control and automation validation in accordance with GAMP5 guidelines is highly preferred.
What Youll Do
Participate in the design and implementation of automation and process control schemes to advance the state of the JPOD continuous manufacturing platform including but not limited to batch tracking establishing process control limits and applying predictive control algorithms.
Maintain global validated DeltaV library and define the governance and global change management for the DeltaV platform to maintain alignment across the manufacturing network
Participate in defining global software development life cycle (SDLC) and global roadmap for DeltaV
Participate in engagement with Site MSAT Automation teams to support global and site objectives
Develop or improve detailed specification qualification (IQ/OQ/PQ) engineering SOP and training documents.
Collaborate with multiple disciplines including manufacturing process engineering process development data scientists utility operations maintenance quality assurance and validation to implement operational improvements
Author and execute test scripts or validation protocols
Lead or contribute to technical root cause analysis incident investigations and troubleshooting of process control issues
Provide technical support to the manufacturing sites as needed specific to process control and automation infrastructure
Provide project oversight or drive progress on PAS implementation projects contracted to 3rd party suppliers/integrators with some guidance from team lead
Who You Are
Education & Experience
Bachelors or Masters degree in Engineering Computer Science or related field with 5 years of relevant experience; OR
Associates degree in a science-related field with 8 years of relevant experience; OR
High school diploma or GED with 10 years of relevant experience.
2 years in pharmaceutical biotech or life sciences industries in a GxP-regulated environment.
Strong control system automation background. Design installation programming and validation of automated processes is essential.
Understanding of FDA CFR 21 Part 11 compliance
Established record of successful project completions employing proven engineering and project management skills
Demonstrated skills coding in DeltaV
Motivated self-starter with strong organizational skills.
Travel & Flexibility
Occasional travel to our JEB Toulouse site (France) for global alignment.
Flexible hours to accommodate collaboration with European teams.
Additional Preferred Qualifications
Previous experience in computer software validation
Participation on global teams Center of Excellence etc.
Leverage expertise using GAMP5 risk-based approach when implementing changes to the validated PAS
Authority inspection or audit support involvement
Experience with single-use technologies and systems
Experience with Siemens Allen Bradley Wonderware automation platforms
Are You Still Curious
If youve read this far then chances are youve got a curious mindjust like us. So what are you waiting for Take the leap and apply today. We cant wait to see where your curiosity leads youand how it will shape the future of Just Evotec Biologics.
Let your curiosity guide your career#BeCurious and explore the endless possibilities at Just Evotec Biologics!
The base pay range for this position at commencement of employment is expected to be $112560 to $154100; 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:
Senior IC
Employment Type
Full-Time
