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Associate Director, Head of Production Engineering

Takeda Pharmaceutical
Posted 4 days ago, valid for a year
Location

Social Circle, GA 30025, US

Salary

$50 - $60 per hour

info
Contract type

Full Time

Life Insurance
Disability Insurance
Tuition Reimbursement

By applying, a Takeda Pharmaceutical account will be created for you. Takeda Pharmaceutical's Terms of Use and Privacy Policy will apply.

Sonic Summary

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  • The Associate Director at Takeda will lead a technical team to align departmental goals with budget and schedule requirements, requiring a bachelor's degree in a related field and at least 8 years of experience, including 3 years in management.
  • The role involves developing and implementing new processes for manufacturing operations, managing technical staff, and ensuring compliance with safety and quality regulations.
  • Candidates should have expertise in engineering disciplines, knowledge of GMPs and FDA guidelines, and proficiency in MS Office and project management software.
  • The position offers a base salary range of $149,100 to $234,300, with potential short-term and long-term incentives, as well as a comprehensive benefits package.
  • The work environment may include physical demands such as lifting up to 50 pounds and working in controlled or loud areas, with a focus on employee safety and regulatory compliance.

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 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:

You will direct technical team to ensure company, site and departmental goals are within budgetary and schedule guidelines. The associate director provides general direction to technical staff, based on technical expertise. The associate director uses understanding of automation MES, theories and practices of a variety of disciplines to manage an operational support function in compliance with all safety and quality regulations and procedures.

Develop and implement new processes for supporting the site manufacturing operations. Coordinate, plan and schedule tasks and activities for supporting site production activities. Define scope of work for project team. Manage, hire, develop and recognize technical staff; create employee and organizational development, and HR plans which meet our needs. Apply specialized knowledge in a creative way to a broad range of difficult problems.

Analyze proposals to determine if benefits derived and possible applications justify expenditures. Approve and submit proposal to Sr. Management. Responsible for policy setting and defining procedures for the staff in accomplishing and documenting work.

Approve protocols and support documentation (engineering change requests, system change forms) to secure project release. Develop staff members to assume technical approver role. You will report to the Head of Fractionation Manufacturing in Social Circle, GA.

How you will contribute:

  • Direct the activities of the department/group.
  • Support site operations:
  • Provide SME level guidance.
  • Support and initiate Continuous Improvement projects where applicable.
  • Represent and support department/group during regulatory audits where applicable.
  • Improve employee utilization to drive continuous improvement.
  • Support daily quality, EHS and PSM activities.
  • Responsible for group annual budget and LRP.
  • Maintain installed building network/systems
  • Daily troubleshooting and monitoring

What You Bring to Takeda:

  • Requires bachelor's degree in science, engineering or other related technical field. 8+ years of related experience with 3+ in a management role.
  • Must be well versed in engineering disciplines (e.g. automation, enterprise wide software , MES, fluid flow, thermodynamics, heat transfer, statics and dynamics, engineering materials). Must have knowledge of related disciplines.
  • Knowledge of GMPs, FDA guidelines (Data Integrity Industry Guidelines, 21CFR part 11, GAMP), purchasing practices and process validation.
  • Maintain industry contacts and be involved in industry interest groups.
  • Fluent with all MSOffice, MSProject, and MSVISIO software
  • Display a strong understanding of automation, information technology and computer system administration good practices, industry standards and regulations.
  • Oversee the development of systems to ensure that those meet the safety, industries regulations, and user requirements (which shall include the maintainability, reliability and scalability of system)
  • Oversee, motivate and direct technical personnel
  • Develop KPIs for responsibilities that help on the continue improvement and performance of the area.
  • Exhibits creativity and new ideas in completing divisional and department responsibilities.
  • Analyze and solve complex problems through creative thought and experience.
  • Manage multiple teams simultaneously.
  • Ability to design outside of immediate scope of responsibility.

Important Considerations:

  • May lift up to 50 pounds.
  • May work in a cold, wet environment.
  • May work in a loud area that requires hearing protection and other protective equipment to be worn.
  • May work around chemicals such as alcohol, acids, buffers that may require respiratory protection.
  • Can work more than 8 hours a day or 40 hours a workweek as required.
  • May work in a confined area as defined by the Environmental, Health, and Safety office.
  • 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.
  • 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.

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 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

#LI-Onsite

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 - GA - Social Circle - Hwy 278

U.S. Base Salary Range:

$149,100.00 - $234,300.00

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 - GA - Social Circle - Hwy 278

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

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By applying, a Takeda Pharmaceutical account will be created for you. Takeda Pharmaceutical's Terms of Use and Privacy Policy will apply.