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Job Description

About the role:

As the Director of Quality Control, you will lead the full scope of Quality Control operations, overseeing analytical chemistry, microbiology, and laboratory excellence to ensure rigorous, reliable, and compliant testing across the organization. You will establish and elevate QC standards, drive alignment with industry and regulatory expectations, and partner closely with Manufacturing and cross‑functional Quality leaders to advance Safety, Quality, Compliance, financial performance, employee development, customer satisfaction, and key digital and continuous improvement initiatives tied to the site’s strategic plan. You will be a visible champion of Takeda’s Quality Culture—Keeping it Simple, Taking Pride in Doing it Right, Ensuring a Speak Up Culture, and Owning and Demonstrating Commitment to Quality—while shaping a high‑performing team and a world‑class laboratory environment. You will report into the Site Quality Head.

How you will contribute:

• Responsible for the QC Laboratory functions, both Analytical Chemistry and Microbiology functions
• Responsible for managing, developing, and implementing compliant processes to ensure highest level of product quality
• Manage 24/7 QC laboratory team who is responsible for testing raw materials, intermediates, and finish drug products
• Ensure compliance with internal standards
• Ensure compliance with industry standards and regulations, staying up to date with any changes or updates
• Act as advisor to subordinates to meet schedules and/or resolve technical problems
• Identify and manage continuous improvement projects that may span multiple sections or departments with the objective of achieving quality, reliability, and cost improvements
• Develop and maintain site contamination control program, with focus on sterility assurance
• Manage overall coaching, training, development and succession plans for the team
• Identify and implement digital innovation for QC laboratory

Minimum Requirements/Qualifications:

• BS in Science, Engineering, or a related field plus 10+ years of experience, 7 of which should be in a management role
• Knowledge of FDA, EMA, CFDA, PDA Regulations, application of Good Data and Documentation Practices (GDDP) and application of current Good Manufacturing Practices
• Experience in interfacing and/or leading regulatory audits
• Demonstrated success in managing a large team
• Must be able to work in controlled environments requiring special gowning. Will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and body
• No make-up, jewelry, contact lenses, nail polish or artificial fingernails may be worn in the manufacturing environment, which in some areas is cold and wet, and require personal protective equipment (PPE). 
• May be required to work in a confined area
• Some Clean Room and cool/hot storage conditions
• Must be able to work multiple shifts, including weekends
• 10% travel

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.

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 - MA - Lexington - BIO OPS

U.S. Base Salary Range:

$174,500.00 - $274,230.00

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-term incentives. 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 - MA - Lexington - BIO OPS

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Job Exempt

Yes

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.