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Supervisor Manufacturing
Supervisor Manufacturing-March 2024
Round Lake Beach
Mar 28, 2026
About Supervisor Manufacturing

  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:

  As the Manufacturing Supervisor implements and manages all activities in the production area at Takeda's Round Lake, Illinois manufacturing facility, to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (cGMPs), environmental health and safety (EHS) guidelines and any other regulations that could apply; focus is on optimization in the use of raw materials, equipment and employees in producing quality products; may monitor and oversees labor and capital expenditures; may help develop budgets; recommend manufacturing policies, procedures and programs.

  The hours of this position are 5PM-5:30AM, 2-2-3; weekend and holiday work. Overtime may be required.

  How you will contribute:

  Provides guidance through positive interactions with all employees during daily operations.

  Manage the daily production, scheduling, staffing, material management, compliance, training and auditing activities – to meet customer requirements including deadlines and quality standards.

  Interview, hires, coaches, motivates, and develops staff; conduct annual performance reviews for all team members; help set performance objectives and development plans; monitors progress.

  Review, approves, and manages documentation for batch and system records; assists in release of product for distribution; help meet product release time goals.

  Emphasize training programs designed to enable staff to complete all manufacturing processes with strict compliance to cGMPs and EHS regulations.

  Develop and implement performance measurement and internal auditing programs to evaluate operation efficiency and quality; implement changes based on assessments.

  Perform technical reviews, investigations and process improvement projects; provide manufacturing input into integration and validation of new equipment and processes.

  Resolve technical, material and cGMP problems that may affect project deadlines; provide guidance and troubleshooting assistance during a deviation in the process.

  Represent the company during FDA inspections; provides information to FDA that establishes credibility and demonstrates compliance with cGMPs.

  Perform daily Gemba walks to engage with employees and ensure their following proper safety practices.

  Demonstrate ability to work with well with other departments and lead in a team environment.

  Experience working in an FDA regulated environment.

  In-depth process knowledge of related manufacturing equipment and processes.

  Prepare technical reports.

  Experience with cGMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry.

  Respond to detailed inquiries, and present information to groups and senior management.

  May supervise multiple groups/shifts.

  Proficient in MS Word, MS Excel.

  What you bring to Takeda:

  High School Diploma or GED plus 4+ years of related experience OR Bachelor's degree in science, engineering or other related technical field and 2+ years of related experience.

  Some leadership experience preferred.

  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 training and 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:

  In general, you will have a combination of sedentary work and walking around observing conditions in the facility.

  Will carry up to 30 lbs., lift up to 30lbs, push/pull up to 30lbs (with assistance of material handling equipment).

  Will stand and walk for an extended period over an 8–12-hour shift between rooms and across the site.

  Indoor working conditions.

  Will work around moving equipment and machinery.

  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 willing to work aligned shift.

  Will work on multiple shifts, including weekends, to support a 24/7 manufacturing operation.

  Will work non-traditional work hours or work extended hours, including weekends and holidays.

  Will work overtime.

  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.

  #GMSGQ

  #ZR1

  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 - IL - Round Lake - Drug Delivery

  Worker Type

  Employee

  Worker Sub-Type

  Regular

  Time Type

  Full time

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