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’sPrivacy Noticeand 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:

Associate Manager, Manufacturing implements and oversees daily activities to ensure manufacturing goals and project deadlines are met by the commitment date while maintaining compliance with the current manufacturing practices (cGMPs), environmental health and safety (EHS) guidelines and any other regulations that could apply. The Associate Manager will improve results to support plant strategic goals. You must enforce company rules, policies and regulations, and promote Takeda values within their team. The Associate Manager will mentor employees to increase performance and behaviors aligned with Takeda's values. It is expected that the Associate Manager set the example for all employees of Takeda. You will promote the appropriate behavior, compliance, and culture of Takeda, including decision-making bases on patient, reputation, and then business (PTRB).

How you will contribute:

• Work with department Managers and Associate Directors and adjust schedule according to fill in for them.
• May be delegate for other areas such as Initial Inspection and Packaging.
• Ensure resources are allocated throughout Inspection & Packaging to allow flow in value chain to exceed production targets.
• Manage production activities throughout Inspection department to ensure manufacturing goals are met.
• Lead escalations by coordinating actions with support groups to follow production schedule, minimize delay, and meet production targets.
• May be assigned leadership roles for larger scope operational projects, such as shutdown and startup and new facilities or processes.
• Champion DMAIC tools for issues that may affect safety, quality, yield, or production.
• Facilitate and verify appropriate training is assigned and completed on time for all employees on the shift (including cGMPs, job skills, safety, etc.).
• Ensure assigned projects, action items, and deliverables are completed per the commitment date.
• Identify, lead, and implement programs to improve site capabilities.
• Implement systems to maintain compliance with current good manufacturing practices (cGMPs), environmental health and safety (EHS) guidelines, FDA, and any other regulations that apply.
• Ensure 100% compliance with established department procedures and regulations in producing high quality therapeutic products.
• Improve performance with employees by providing a positive and equitable work environment emphasizing respect, responsiveness, and results, as well as, using the talent management process.
• Be present at the shift transition with the shift supervisor(s) and ensure shift transition/communication to the next incoming shift.
• Chair Tier 1 meeting of their respective area; may be a backup to chair Tier 2 meetings.
• Hire new manufacturing employees (supervisors and technicians) and participate in interviews for supporting department candidates.
• Participate in project meetings, EHS and QA incident investigations.
• Lead and coordinate facilities GEMBA with supervisors and supporting groups (i.e. Facilities Engineering, QA, Maintenance) to ensure Manufacturing and Supporting areas are at the highest standards and are inspection ready.
• Represent department and providing leadership in meetings, audits and projects.
• Ensure supervisors and employees comply with the QA and EHS investigation timelines.
• Develop staff and oneself through Quality Conversations and development processes.
• Partner with support groups (EHS, Quality, Engineering and Maintenance) to improve safety, quality to meet department goals.
• Must be familiar with all areas within Manufacturing (Inspection & Packaging).
• Analyze statistical information including financial reports.
• Understand and resolve technical problems and interface with engineering/technical experts to resolve issues promptly.
• Perform investigations and communicate through well written documentation.
• Knowledge of world-class manufacturing methods (Lean, Six Sigma), Good Manufacturing Practices, Food Drug and Administration regulations.
• Will work and facilitate a team-oriented environment.
• May supervisor multiple groups and shifts.
• Manager of self and production staff that may include manufacturing supervisors and operators.

What you bring to Takeda:

• Typically requires Bachelors' degree in science, engineering or other related technical field and 5+ years of related experience.
• Leadership experience.

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:

• In general, your work will be a combination of sedentary work and walking around observing conditions in the facility.
• Must be able to lift, push, pull and carry up to 35 lbs.
• May work in a confined area.
• Some Clean Room and cool/hot storage conditions.
• 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.
• Must be able to work multiple shifts, including weekends.
• Non-Exempt Roles only: Will work overtime.
• 5% travel.

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.

#GMSGQ

#ZR1

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:

U.S. Base Salary Range:

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

Worker Type

Worker Sub-Type

Time Type