Senior Automation Engineer - PLC Thousand Oaks, California Category: Manufacturing Engineering

BioLife Plasmazentrum
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Senior Automation Engineer - PLC

Thousand Oaks, California Apply Now Save job Job ID R0185964 Category Manufacturing Engineering Subcategory Manufacturing & Supply Business Unit Global Manufacturing & Supply Job Type Full time

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Job Description

Aboutthe role

The Senior Automation Engineer - PLC provides day-to-day automation engineering support for Formulation, Filling, Packaging, and Utilities operations at the Thousand Oaks site. This role supports automation systems, executes automation projects of varying complexity and scope, and helpsmaintainreliable, compliant, and efficient manufacturing operations.

You will serve as a technical resource for PLC, HMI, SCADA, instrumentation, and control system lifecycle activities in a regulated pharmaceutical environment. The role requires strong hands-on troubleshooting, system administration, project execution, and cross-functional partnership to support production needs and continuous improvement.

The successful candidate will apply sound engineering judgment to resolve complex automation issues,leador support automation projects from concept through finaldesign, andhelp develop robust control strategies aligned with local and global practices.

Howyou will contribute

  • Provide automation engineering support for Formulation, Filling, Packaging, Utilities, and related manufacturing operations.

  • Create control system layouts and integrate PLCs with HMIs, sensors, actuators, instrumentation, and other automation components.

  • Write, debug, test, andmaintainPLC code, including Ladder Logic and related control logic, to support precise, reliable process control.

  • Troubleshoot PLC-based systems and resolve automation faults to minimize downtime and support operational continuity.

  • Administer,maintain, and improve automation platforms used at the Thousand Oaks site, including Allen-Bradley PLC, Siemens SIMATIC WinCC, Siemens PLC S7, andIntellution/ProficyiFixSCADA.

  • Develop improved and robust control system strategies for manufacturing processes using local and global practices.

  • Draft, update, and routinely verify system specifications, SOPs, training materials, and related automation system documentation.

  • Lead or support control system lifecycle activities in a regulated environment, including pharmaceutical change control standards and policies.

  • Train users on control system functionality and provide guidance on programmable logic controllers, process control, control networks, and instrumentation.

  • Serve as a subject matter expert by leading, training, and mentoring automation engineers and technicians as requested.

  • Plan and execute automation projects, or defined portions of larger projects, with minimal guidance, including schedules, cost estimates, business case justifications, and cross-functional coordination.

  • Contribute to costestimating formajor capital budget items, approved project spending, financial planning, and analysis to justify project approval.

  • Investigatecustomer-serviceand manufacturing support issues, analyze root causes, and recommend design or process improvements.

  • Manage small routine projects with complex features and coordinate contractors, technicians, and cross-functional teams as needed.

  • Provide automation support through on-call coverage during off-hours as part of a 24/7 operation.

  • May perform other duties as assigned.

Whatyou bring to Takeda

  • Bachelor’s degree inan engineering field.

  • Minimum of 7 years of PLC automation orcontrolsexperience in a GMP pharmaceutical or similar regulated environment.

  • Experience with automation system instrumentation and field device technology.

  • Experience with control systems, including Allen-Bradley PLC andIntellution/iFixSCADA.

  • Strong understanding of basic engineering principles across multiple engineering disciplines.

  • Ability to troubleshoot and solve routine design, process, and automation engineering problems independently.

  • Ability to prioritize multiple tasks from multiple customers and elevate issues whenappropriate.

  • Strong verbal and written communication skills, including the ability to discuss technical issues clearly and present technical or project management updates.

  • Ability to work collaboratively and effectively lead, train, or support less experienced engineers, technicians, contractors, and cross-functional teams with minimal guidance.

  • Demonstrated ability to adapt in a fast-paced and constantly evolving environment.

Preferred capabilities

  • Knowledge ofcGxPmanufacturing and processes.

  • Knowledge of pharmaceutical production equipment, including critical utilities, autoclaves, parts washers,lyophilizers, process tanks, filling machines, and CIP/SIP systems.

  • DeltaVexperience.

  • Ability todemonstratecreativity and innovation when supporting divisional, cross-functional, or business-unit responsibilities.

Importantconsiderations

At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering product quality. In this role, you maybe requiredto follow site-specific safety, gowning, andcontrolled-environmentexpectations.

This role may involve field work around robotic systems, control instrumentation, wiring, and control panels. The role isgenerally sedentarybut may require lifting, pushing, pulling, or carrying up to 25 lbs.

The working environment may include controlled areas requiring special gowning, loud areas requiring hearing protection, and areas with chemicals such as alcohol, acids, buffers, and celite that may require respiratory protection.

This role may require work beyond standard business hours, including weekends and holidays, and may require availability outside of business hours to support 24/7 operations.

Moreabout us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best-in-class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Empoweringour people to shine:

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

For Location:

USA - CA - Thousand Oaks - Rancho Conejo

U.S. Base Salary Range:

$89,900.00 - $141,240.00

The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. 

U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. 

EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

LocationsUSA - CA - Thousand Oaks - Rancho Conejo

Worker TypeEmployee

Worker Sub-TypeRegular

Time TypeFull time

Job Exempt

Yes

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Hauptstandort

BioLife Plasmazentrum

Industriestraße 67
1221 Wien
Österreich

BioLife Plasmazentrum - image

BioLife Plasmazentrum

Wien

Rund 30.000 Menschen spenden jedes Jahr bei BioLife in Österreich Blutplasma. Daraus entstehen Medikamente, die sich nicht künstlich herstellen lassen und Patientinnen und Patienten mit angeborenen oder erworbenen Erkrankungen oft ein Leben lang begleiten. Vierzehn Zentren betreibt BioLife dafür im Land, von Wien bis Villach. Hinter der Marke steht Takeda.

Der japanische Biopharma-Konzern führt die österreichischen Zentren über die Takeda Manufacturing Austria AG mit Sitz in Wien-Donaustadt und beschäftigt in Österreich rund 4.500 Menschen, von der Forschung über die Plasmaaufbringung bis zur Produktion in Wien und Linz. Österreich ist damit der größte Standort im weltweiten Takeda-Netzwerk. Das gespendete Plasma bleibt großteils im Land: In Wien wird es zu Arzneimitteln weiterverarbeitet, im Qualitätskontrolllabor in Orth an der Donau geprüft. Wer in einem Zentrum arbeitet, steht also am Anfang einer Wertschöpfungskette, die im selben Land endet.

Die Tradition ist älter, als der Markenname vermuten lässt. Das erste Plasmazentrum Europas öffnete 1964 in Wien. Sein 60-jähriges Bestehen feierte BioLife im Juni 2024 mit der Eröffnung des vierzehnten österreichischen Zentrums in der Villacher Postgasse, wo auf 500 Quadratmetern bis zu 22 Personen gleichzeitig spenden können. Ein Jahr davor war in Linz das dreizehnte Zentrum entstanden, das erste weltweit, das sich emissionsfrei betreiben lässt. Es brachte 25 neue Arbeitsplätze in die Stadt, in der Takeda ohnehin schon rund 700 Menschen beschäftigt.

Die Arbeit im Zentrum ist nah am Menschen. Ärztinnen und Ärzte aus der Allgemeinmedizin, der Transfusionsmedizin oder der Inneren Medizin beurteilen die Spendetauglichkeit und betreuen die Spendenden medizinisch, Pflegefachkräfte punktieren und begleiten die Plasmapherese, medizinische Assistenzkräfte führen durch Anmeldung und Dokumentation. Ausgeschrieben werden solche Stellen laufend in Graz, Klagenfurt und Wien. Ein Argument für viele im Gesundheitsbereich: Die Zentren haben feste Öffnungszeiten, und laut Arbeitgeberprofil auf karriere.at fallen weder Nacht- noch Wochenenddienste an, dazu kommen Essens- und Öffi-Zuschuss sowie Weiterbildung und Mentoring. Rund 500 geschulte Mitarbeitende sind es in den vierzehn Zentren zusammen.

Klicke hier,
um mit der Karte zu interagieren.

Hauptstandort

BioLife Plasmazentrum

Industriestraße 67
1221 Wien
Österreich