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　　Job Description

　　About the role:

　　The Supervisor position implements and supervises daily activities in a specific production area to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (GMPs), environmental health and safety (EHS) guidelines and any other regulations that could apply. May manage labor resources.

　　The hours of this position are 6PM-6:30AM; 2-2-3 weekend and holiday work. Overtime may be required.

　　How you will contribute:

　　Supervise the daily manufacturing operations in an area. Maintain (audit, refine, improve) equipment and processes within this area.

　　Provide a positive and equitable working environment emphasizing respect, responsiveness and results.

　　Support and emphasize the Safety and Quality commitments of the department. Make decisions concerning these commitments within the area.

　　Utilize resources and raw materials in the most efficient and productive manner possible.

　　Identify/prioritize/provide resources in an area to assist the superintendent to meet the annual operational plan and budgetary commitments.

　　Facilitate and verify appropriate training for employees in the area (including GMP, job skills, safety).

　　Ensure compliance with all GMP rules, product documentation, specifications, SOPs, and FDA requirements.

　　Commit to employee feedback and developmental process – support Talent Management goals, conduct recognition and disciplinary action for employees, facilitate employee representation throughout the organization.

　　Submit and maintain and distribute reports related to attendance, labor, efficiency, safety, scrap and others.

　　What you bring to Takeda:

　　Typically requires bachelor's degree preferred in science, engineering or other related technical field. 3+ years of related experience with 1+ years in a supervisor role.

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

　　Manage multiple processes in a manufacturing plant setting.

　　Write and ability to prepare technical documents.

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

　　Assessment and troubleshooting skills.

　　Work with all levels of personnel to resolve issues related to manufacturing, Quality, documentation, and personnel issues.

　　Work in and facilitate a team-oriented environment.

　　Collect and analyze data to determine paths for process improvement and potential cause/corrective actions in the case of exceptions.

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

　　Manage multiple groups.

　　May require immunization before performing work within the manufacturing area

　　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:

　　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.

　　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.

　　Some clean room and cool/hot storage conditions.

　　Work multiple shifts, including weekends, or be asked to work supplemental hours.

　　Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.

　　Will carry up to 25 lbs., lift up to 50 lbs., and push/pull > 100 lbs. (with the assistance of material handling equipment).

　　Will stand for extended periods of time over an entire 8 or 12-hour shift.

　　Will climb ladders and stairs while wearing special gowning.

　　Will require bending, twisting, reaching overhead, and squatting motions to perform certain tasks.

　　May require immunization before performing work within the manufacturing area.

　　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

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　　#LI-MA1

　　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 - GA - Social Circle - Hwy 278

　　Worker Type

　　Employee

　　Worker Sub-Type

　　Regular

　　Time Type

　　Full time