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Supervisor Manufacturing - Nights

Employer
Takeda
Location
Round Lake Beach, Illinois
Start date
May 22, 2024

Job Details

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:

The Production Supervisor is responsible for implementing and supervising 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 assist in developing budgets; recommends manufacturing policies, procedures and programs. This position is a 2-2-3 rotating shift reporting to D Shift (6:00 PM - 6:00 AM).

How you will contribute:
  • Provides guidance, support, direction, and leadership through positive interactions with all employees during daily operations.

  • Supervises the day-to-day production, scheduling, staffing, material management, compliance, training and auditing activities – to meet customer requirements including deadlines and quality standards.

  • Interviews, hires, coaches, motivates, develops and disciplines staff; conducts annual performance reviews for all team members; assists in setting performance objectives and development plans; monitors progress.

  • Reviews, approves, and manages documentation for batch and system records; assists in release of product for distribution; assists in meeting product release time goals.

  • Emphasizes training programs designed to enable staff to consistently execute all manufacturing processes with strict compliance to cGMPs and EHS regulations.

  • Develops and implements performance measurement and internal auditing programs in order to routinely evaluate operation efficiency and quality; implements changes as needed based on assessments.

  • Performs/leads technical reviews, investigations and process improvement projects; provides manufacturing input into integration and validation of new equipment and processes.

  • Resolves technical, material and cGMP problems that may impact project deadlines; provides guidance and troubleshooting assistance as needed during a deviation in the process.

  • Represents the company during FDA inspections; provides information as necessary to FDA that establishes credibility and demonstrates compliance with cGMPs.

  • Performs daily gemba walks to engage with employees and ensure their following proper safety practices.

  • Demonstrated interpersonal and leadership skills with ability to interface well with other departments and lead effectively and efficiently in a team environment.

  • Experience working in an FDA regulated environment preferred.

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

  • Ability to manage multiple priorities in a manufacturing plant setting.

  • Ability to analyze and interpret scientific and statistical data.

  • Have strong teamwork and communication skills, both verbally and written, good documentation skills, customer oriented, work safely and effectively under stressful conditions.

  • Strong professional writing skills and ability to prepare technical reports.

  • Experienced understanding of cGMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry.

  • Strong assessment and troubleshooting skills.

  • Ability to respond to detailed inquiries, and present information to groups and senior management.

  • May be required to supervise multiple groups/shifts.

  • Good computer skills. Proficient in MS Word, MS Excel.

What you bring to Takeda:
  • High School Diploma or GED plus 4+ years of related experience OR Bachelors' degree in science, engineering or other related technical field and 2+ years of related experience. Some leadership experience preferred.

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 willing and able to work aligned shift.

  • In general, the position requires a combination of sedentary work and walking around observing conditions in the facility.

  • Must be able to carry up to 30 lbs., lift up to 30lbs, push/pull up to 30lbs (with assistance of material handling equipment).

  • Must be able to stand and/or 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.

  • Some Clean Room and cool/hot storage conditions

  • May be required to work in a confined area.

  • 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/or 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.

  • Must be able to work overtime as required.

  • Must be able to work on multiple shifts, including weekends, to support a 24/7 manufacturing operation as needed.

  • Must be able to work non-traditional work hours or work extended hours, including weekends and holidays, as needed.

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.

#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:

USA - IL - Round Lake - Drug Delivery

U.S. Base Salary Range:

$84,000.00 - $132,000.00

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-termincentives. 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.

Locations

USA - IL - Round Lake - Drug Delivery

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Company

Takeda is a global, values-based, R&D-driven biopharmaceutical leader headquartered in Japan, committed to discover and deliver life-transforming treatments, guided by our commitment to patients, our people and the planet. Takeda focuses its R&D efforts on four therapeutic areas: Oncology, Rare Genetics and Hematology, Neuroscience, and Gastroenterology (GI). We also make targeted R&D investments in Plasma-Derived Therapies and Vaccines. We are focusing on developing highly innovative medicines that contribute to making a difference in people’s lives by advancing the frontier of new treatment options and leveraging our enhanced collaborative R&D engine and capabilities to create a robust, modality-diverse pipeline. Our employees are committed to improving quality of life for patients and to working with our partners in health care in approximately 80 countries and regions.

For more information, visit https://www.takeda.com.

Stock Symbol: TAK

Company info
Website
Location
650 East Kendall Street
Cambridge
MA
02421
US

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