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Job Description
About the role:
The Manufacturing Tech IV helps implement processes in production while strictly following cGMP, environmental health and safety guidelines and any other related regulations which could apply. You will participate in both departmental projects and any quality working teams which may be applicable. Under the direction of the Supervisor and Manufacturing Lead, this position shall aid in the leadership and execution of activities in the production area. When the Manufacturing Lead is absent, the Manufacturing Tech IV may be their delegate. You will use DMAIC methodology, implement Preventive Maintenance and manage the assembly and disassembly of the centrifuges, Mechanical Troubleshooting and repair. In addition to the manufacturing responsibilities described in this job description, they may be asked to problem solve in other areas. You will understand the regulations and may make recommendations according to their interpretations. They will have technical and administrative knowledge to perform complex troubleshooting tasks on manual and automated equipment and assist during the transfer of new processes/methodologies into the manufacturing area. Manufacturing Tech IV will set the example for other Takeda employees as their team members observe the behavior of their leadership and interpret that behavior as acceptable. You will always promote Takeda's focus on Patient, Trust, Reputation, and Business.
How you will contribute:
Responsible for the assembly and disassembly of the centrifuges in the manufacturing area
Attend weekly/biweekly centrifuge meetings
Expected to work with engineering and maintenance regarding ideas for improvement and corrective work.
Execute the Centrifuge Troubleshooting Guidelines.
Maximize the life of centrifuge bowls, components, tools, and ancillary support equipment thru operator care principles.
Oversee and assist with on-the-job training of other Manufacturing Techs on SOPs for centrifuge assembly, disassembly, and operations
Follow safety rules, SOPs, cGMP, work rules and other company policies and programs.
Complete relevant paperwork following GDP/GMP guidelines.
Perform hands-on execution of manual and automated manufacturing operations. Equipment may include: Centrifuges, Filter Presses, Ultrafiltration systems, CIP/COP, Nano-filtration Skids, Chromatography Columns and material handling devices. Manual activities include weighing and addition of chemicals, paste suspension, equipment cleaning, room cleaning, equipment assembly/disassembly, transfer panel connections, titrations and other activities.
Receive and distribute supplies into the production area.
Troubleshoot process problems and respond to process alarms.
What you bring to Takeda:
Must pass the centrifuge written proficiency test and pass the hands-on assembly/disassembly test. Recertification may be required. (Applicable to Centrifuge SME role)
In-depth process knowledge of related manufacturing techniques and specialties.
Advanced automation experience using DeltaV, Electronic Batch Management, PLC.
Familiarity with pharmaceutical production equipment including centrifuges, filtration systems and CIP/SIP (Clean in Place/Steam in Place).
Experience operating material handling equipment such as pallet jacks and forklifts.
Must have and a understanding of cGMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry.
Knowledge of basic chemical and biological safety procedures.
Experience in DeltaV, Manufacturing Execution Systems, scheduling software or similar systems.
Basic knowledge of instrumentation and mechanical such as controllers, indictors, control valves, PLC, analyzers, sensors, pumps.
Education:
High school diploma or GED. 4+ years of related work experience or AA degree or higher and 2+ years related work experience.
Mechanical, electrical, instrumentation, or control systems repair experience preferred for preventative maintenance subject matter expertise role.
Must be able to lift, push, pull and carry up to 50 lbs.
Must be able to stand for extended periods of time throughout the duration of an 8- or 12-hour shift.
Must be able to climb ladders and stairs while wearing special gowning.
May require bending, twisting, reaching, and/or squatting motions to perform certain tasks.
In general, the position requires a combination of sedentary work and walking around observing conditions in the facility
What Takeda can offer you:
Comprehensive Healthcare: Medical, Dental, and Vision
Financial Planning & Stability: 401(k) with company match and Annual Retirement Contribution Plan
Health & Wellness programs including onsite flu shots and health screenings
Generous time off for vacation and the option to purchase additional vacation days
Community Outreach Programs and company match of charitable contributions
Family Planning Support
Professional development opportunities
Tuition reimbursement
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. In this role, you may:
Must be able to lift, push, pull and carry up to 50 lbs.
Will stand for extended periods of time throughout the duration of an 8- or 12-hour shift.
Must be able to climb ladders and stairs while wearing special gowning.
May require bending, twisting, reaching, and squatting motions to perform certain tasks.
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.
Must be able to work multiple shifts, including weekends.
Need to remove all make-up, jewelry, contact lenses, nail polish and artificial fingernails while in the manufacturing environment.
Work in a cold, wet environment.
Work multiple shifts, including weekends, or be asked to work supplemental hours, as necessary.
Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.
More about 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.
This posting excludes Colorado applicants.
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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.
Locations
USA - CA - Los AngelesWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full time
