BioSpace
Overview
Join to apply for the
Director Quality Control
role at
BioSpace . About the Site/Role
Located just outside Atlanta, Takeda’s state-of-the-art manufacturing facility in Covington is one of the largest biotech production sites in the world. As a pivotal part of Takeda’s global manufacturing network, the Covington site plays a key strategic role in supplying high-quality plasma-derived therapies to patients worldwide. Equipped with advanced technology and modern processes, the facility supports ongoing innovation, helping to drive Takeda’s growth and mission to deliver life-changing medicines. As our Quality Control Leader, you will guide and support all quality control activities at our site, encompassing analytical chemistry, microbiology, and adherence to laboratory best practices. Your work will be crucial in ensuring we meet high standards for product safety, compliance, and continuous improvement. You’ll report directly to the Site Quality Head and be a visible champion of Takeda’s Quality Culture. How You Will Contribute
Lead and manage the Quality Control (QC) Laboratory, including the Analytical Chemistry and Microbiology teams. Develop and uphold quality control processes to guarantee product safety and compliance. Manage a QC team responsible for 24/7 testing of raw materials, intermediates, and finished products. Ensure all operations meet internal and external (regulatory) quality standards and stay current with new requirements. Hire, develop, and recognize technical staff; foster a culture of growth and acknowledgment. Serve as a key advisor and handle technical issues and scheduling for the QC team. Evaluate the effectiveness of quality control activities with site leadership. Lead and drive continuous improvement initiatives focused on quality, reliability, and cost savings, including digital projects. Manage the budget for the QC department. Develop and maintain the site contamination control program with a focus on sterility assurance. What You Bring To Takeda
Bachelor’s degree in science, engineering, or a related technical field (or equivalent experience). At least 10 years of relevant experience, including 7+ years in a leadership role. Strong background in managing large, multi-function laboratories and extensive experience in Analytical Chemistry. Solid understanding of regulatory requirements (FDA, EMA, cGMP, GDDP). Experience managing regulatory inspections and audit readiness. Familiarity with laboratory testing for endotoxin and sterility (preferred). Effective at managing budgets and team development. Experience with digital and process improvement initiatives. Important Considerations
Physical requirements and working conditions include cleanroom environments with gowning, PPE, and potential exposure to chemicals and biological agents. Work in a clean, controlled environment that may require special clothing; be comfortable in areas that may be cold, hot, or have confined spaces; clean room and variable storage conditions apply. Ability to work multiple shifts, including weekends or overtime as needed. Up to 10% travel may be required. 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 on-site flu shots and health screenings Generous paid time off for vacation, sick leave, and volunteering Community Outreach Programs and company match of charitable contributions Family Planning Support Professional development and training opportunities Tuition reimbursement 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. Locations: USA - GA - Social Circle - Hwy 278 Job Details
Seniority level: Director Employment type: Full-time Job function: Quality Assurance Industries: Internet News 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.
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Join to apply for the
Director Quality Control
role at
BioSpace . About the Site/Role
Located just outside Atlanta, Takeda’s state-of-the-art manufacturing facility in Covington is one of the largest biotech production sites in the world. As a pivotal part of Takeda’s global manufacturing network, the Covington site plays a key strategic role in supplying high-quality plasma-derived therapies to patients worldwide. Equipped with advanced technology and modern processes, the facility supports ongoing innovation, helping to drive Takeda’s growth and mission to deliver life-changing medicines. As our Quality Control Leader, you will guide and support all quality control activities at our site, encompassing analytical chemistry, microbiology, and adherence to laboratory best practices. Your work will be crucial in ensuring we meet high standards for product safety, compliance, and continuous improvement. You’ll report directly to the Site Quality Head and be a visible champion of Takeda’s Quality Culture. How You Will Contribute
Lead and manage the Quality Control (QC) Laboratory, including the Analytical Chemistry and Microbiology teams. Develop and uphold quality control processes to guarantee product safety and compliance. Manage a QC team responsible for 24/7 testing of raw materials, intermediates, and finished products. Ensure all operations meet internal and external (regulatory) quality standards and stay current with new requirements. Hire, develop, and recognize technical staff; foster a culture of growth and acknowledgment. Serve as a key advisor and handle technical issues and scheduling for the QC team. Evaluate the effectiveness of quality control activities with site leadership. Lead and drive continuous improvement initiatives focused on quality, reliability, and cost savings, including digital projects. Manage the budget for the QC department. Develop and maintain the site contamination control program with a focus on sterility assurance. What You Bring To Takeda
Bachelor’s degree in science, engineering, or a related technical field (or equivalent experience). At least 10 years of relevant experience, including 7+ years in a leadership role. Strong background in managing large, multi-function laboratories and extensive experience in Analytical Chemistry. Solid understanding of regulatory requirements (FDA, EMA, cGMP, GDDP). Experience managing regulatory inspections and audit readiness. Familiarity with laboratory testing for endotoxin and sterility (preferred). Effective at managing budgets and team development. Experience with digital and process improvement initiatives. Important Considerations
Physical requirements and working conditions include cleanroom environments with gowning, PPE, and potential exposure to chemicals and biological agents. Work in a clean, controlled environment that may require special clothing; be comfortable in areas that may be cold, hot, or have confined spaces; clean room and variable storage conditions apply. Ability to work multiple shifts, including weekends or overtime as needed. Up to 10% travel may be required. 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 on-site flu shots and health screenings Generous paid time off for vacation, sick leave, and volunteering Community Outreach Programs and company match of charitable contributions Family Planning Support Professional development and training opportunities Tuition reimbursement 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. Locations: USA - GA - Social Circle - Hwy 278 Job Details
Seniority level: Director Employment type: Full-time Job function: Quality Assurance Industries: Internet News 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.
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