On the Global Manufacturing and Supply (GMS) team at Takeda, you'll be part of a rapidly transforming industry that's applying technology and data in new ways. Within our agile, innovative, people-centric organization, your work will matter every day as you use your skills to help us manufacture therapies for patients on our four platforms:

• Small Molecules
• Biologics
• Plasma
• Cell and Gene

As part of the GMS team, you'll have the opportunity to pursue unique experiences and build new skills, and you'll know that the work you do every day makes an impact - on our patients, our people, our planet, and on yourself.

Job ID R Date posted 06/13/2024 Location Thousand Oaks, California

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description About the role: Under the direction of the Head of Process Engineering, you will provide support for operations and projects for manufacturing at the Rancho and Lawrence Manufacturing Facilities. You will report to the Head of Process Engineering.

How you will contribute:

• Demonstrate engineering practices that support operations while improving functionality.
• Apply engineering principles to the design and implementation of major system modifications, process and capital projects.
• Build engineering tasks, make design recommendations with the area leader and assess results for validity and specifications.
• Support manufacturing issues, investigations, and improvements as it relates to process engineering.
• Provide technical expertise for troubleshooting manufacturing process and equipment problems.
• Determine basic causes, develop recommendations for corrective action, and follow-up to ensure completion of corrective action.
• Responsible for all manufacturing equipment life cycle.
• Recommend techniques to improve existing products/processes to improve production efficiency and to reduce cycle time.
• Investigate new sources for raw materials or processes, analyze customer service problems and design improvement suggestions.
• Lead process improvement projects through implementation, training on new processes and measure systems.
• Run projects, qualify equipment, coordinate contractors, and direct the activities of technicians.
• Report project costs, estimate impacts of design/policy changes, and recommend capital expenditures and production methods with the area leader.
• Organize and present technical and project management overviews.
• Use engineering tools to solve straightforward problems (e.g., FMEA, Process Modeling, Design of Experiments, software development).
• Provide solutions that reflect understanding our goals and cost possible effects.
• Analyze how process changes will affect overall production and the product.
• Ensure CGMPs, SOPs, Company Procedures, and Good Engineering Practices are integrated in all activities.
• Through understanding on Packaging Machines and Aseptic processes, Single- Use Equipment, Filling Machines (Isolator and RAB technology), Capping Machines, Parts Washers, Autoclaves, Lyophilizers, CIP/SIP Systems.
• General knowledge of basic principles in different engineering disciplines.
• Knowledge of cGMP manufacturing and GEP.
• Technical writing skills.

What you bring to Takeda:

• B.S. in Engineering is required - Chemical or Mechanical Engineering.
• Minimum 5 years of related experience (in-house, co-op or acquired outside) in a GMP pharmaceutical environment.

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 the quality of the product. You may:

• Able to lift, push, pull and carry up to 25 lbs.
• Combination of sedentary work and walking around observing conditions in the facility.
• May work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas.
• Will need to remove all make-up, jewelry, contact lenses, nail polish and artificial fingernails while in the manufacturing environment.
• May work in a cold, hot or wet environment.
• May work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.
• Can work more than 8 hours a day or 40 hours a workweek.
• May participate in process engineering on-call program.
• May require availability outside regular business hours.

More about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and the best patient support programs. Takeda is a patient-focused company to 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.

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 By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description About the role: Under the direction of the Head of Process Engineering, you will provide support for operations and projects for manufacturing at the Rancho and Lawrence Manufacturing Facilities. You will report to the Head of Process Engineering.

How you will contribute:

• Demonstrate engineering practices that support operations while improving functionality.
• Apply engineering principles to the design and implementation of major system modifications, process and capital projects.
• Build engineering tasks, make design recommendations with the area leader and assess results for validity and specifications.
• Support manufacturing issues, investigations, and improvements as it relates to process engineering.
• Provide technical expertise for troubleshooting manufacturing process and equipment problems.
• Determine basic causes, develop recommendations for corrective action, and follow-up to ensure completion of corrective action.
• Responsible for all manufacturing equipment life cycle.
• Recommend techniques to improve existing products/processes to improve production efficiency and to reduce cycle time.
• Investigate new sources for raw materials or processes, analyze customer service problems and design improvement suggestions.
• Lead process improvement projects through implementation, training on new processes and measure systems.
• Run projects, qualify equipment, coordinate contractors, and direct the activities of technicians.
• Report project costs, estimate impacts of design/policy changes, and recommend capital expenditures and production methods with the area leader.
• Organize and present technical and project management overviews.
• Use engineering tools to solve straightforward problems (e.g., FMEA, Process Modeling, Design of Experiments, software development).
• Provide solutions that reflect understanding our goals and cost possible effects.
• Analyze how process changes will affect overall production and the product.
• Ensure CGMPs, SOPs, Company Procedures, and Good Engineering Practices are integrated in all activities.
• Through understanding on Packaging Machines and Aseptic processes, Single- Use Equipment, Filling Machines (Isolator and RAB technology), Capping Machines, Parts Washers, Autoclaves, Lyophilizers, CIP/SIP Systems.
• General knowledge of basic principles in different engineering disciplines.
• Knowledge of cGMP manufacturing and GEP.
• Technical writing skills.

What you bring to Takeda:

• B.S. in Engineering is required - Chemical or Mechanical Engineering.
• Minimum 5 years of related experience (in-house, co-op or acquired outside) in a GMP pharmaceutical environment.

Important Considerations 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 the quality of the product. You may:

• Able to lift, push, pull and carry up to 25 lbs.
• Combination of sedentary work and walking around observing conditions in the facility.
• May work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas.
• Will need to remove all make-up, jewelry, contact lenses . click apply for full job details