Director Automation Biotechnology & Pharmaceuticals - Redmond, OR at Geebo

Director Automation

Director Automation- Global MSATThe Director Automation is responsible for leading the Automation Team in Global MSAT.
This role is responsible for defining the process control automation system and manufacturing execution system standards for the J.
POD Manufacturing platform, ensure alignment across the J.
POD network, as well as provide process automation support to Just-Evotec s biologics manufacturing sites.
This individual is expected to have an advanced proficiency and leadership in DeltaV process control automation (SCADA and DCS) as well as PAS-X MES deployment, configuration, and integration to other automation systems.
Experience working in a GMP environment, change control, and automation validation in accordance with GAMP5 guidelines is expected.
Responsibilities:
Report to the VP of Global MSAT and leads the Global Automation Team.
Responsible for recruitment and employee development in the automation organization.
Lead the design and implementation of new process digital systems, automation and process control schemes to advance the state of the J.
POD continuous manufacturing platformDefine global software development life cycle (SDLC) and global roadmap for DeltaV, MES, and other process digital systemsPartner with Site MSAT Automation teams to lead or support global and site objectivesDefine strategy for the development or improvement of detailed specification, qualification (IQ/OQ/PQ), engineering, SOP, and training documentsCollaborate with multiple disciplines, including manufacturing, process engineering, process development, data scientists, utility operations, maintenance, quality assurance, and validation to lead implementation of operational improvementsProvide digital systems project oversight or lead complex implementation projects contracted to 3rd party suppliers/integratorsPosition Requirements:
B.
S or M.
S.
in Electrical Engineering or Computer Science, Chemical Engineering, Biotech Engineering, or related life science engineering15
years relevant experience in pharmaceutical, biotech, or life sciencesStrong process automation background and experience in design, installation, programming, and validation of automated processesUnderstand FDA CFR 21 Part 11 complianceEstablished record of leading successful project completions employing proven engineering and project management skillsDemonstrated leader of automation teamsCandidate must possess strong focus on quality and attention to detailMotivated, self-starter with strong organizational skillsGood interpersonal, team, leadership, and communication skills are a mustPrevious experience in computer software validationAdditional Preferred
Qualifications:
Lead roles on Global teams, Center of Excellence, etc.
Previous roles as a digital system Business Process OwnerLeverage expertise using GAMP5 risk-based approach when implementing changes to the validated PASAuthority inspection or audit support involvementExperience with DeltaV and PAS-XWorking knowledge of biomanufacturing upstream and downstream process operations and process control strategies.
The base pay range for this position at commencement of employment is expected to be $127,050 - $235,950; 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.
SummaryLocation:
RedmondType:
Full time.
Estimated Salary: $20 to $28 per hour based on qualifications.

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