Quality Control Analyst II
Job
USA - 3390 Baxalta U.S., Inc.
Covington, GA (In Person)
$92,330 Salary, Full-Time
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Job Description
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's Privacy 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:
As a Quality Control Analyst II, you will perform compendial assessments to ensure compliance with current regulatory requirements and pharmacopeial standards. You will author and review technical documents, including protocols, standard operating procedures (SOPs), and analytical methodologies and design and coordinate analytical method onboarding activities, including execution planning, training, and documentation.How you will contribute:
Lead and manage the qualification of critical materials, ensuring fitness for use in analytical testing. Oversee change control management processes, including risk assessment, documentation, and implementation. Manage Corrective and Preventive Actions (CAPAs) related to analytical processes and support timely closure of quality events. Act as a Subject Matter Expert (SME) by providing technical guidance and troubleshooting support to laboratory testing teams. Collaborate effectively across departments to ensure alignment and successful execution of cross-functional initiatives. Identify and drive continuous improvements in analytical methods and laboratory workflows to enhance efficiency and compliance. Conduct data trending and analysis of laboratory processes and analytical performance on a routine basis to identify trends and areas for improvement. Collaborate as a QC representative with global teams on both global and local projects and take the initiative for improvements. All other duties as assigned by Leadership What you bring toTakeda:
Requires bachelor's degree in science, engineering, or other related technical field. 2-5 years of related experience in pharmaceutical or similar regulated industry. Must know quality laboratory operations and government regulations pertaining to pharmaceutical and medical device manufacturing labs. Must have the ability to manage multiple tasks and responsibilities for the QC Lab. Must have the ability to manage complex projects and resolving complex lab issues. Must possess excellent technical and interpersonal skills and be able to communicate with all level personnel and regulatory authorities. Advanced knowledge in Statistical Analysis and cGMP standards, preferred. Strong leadership, project and people management skills, and ability to make critical decisions. Strong understanding of business and/or industry.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/or 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, as necessary. 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 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 #LI-MA1 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.
Base Salary Range:
$71,800.00- $112,860.
- GA•Social Circle•Hwy 278 Worker Type Employee Worker Sub-Type Regular Time Type Full time Job Exempt Yes Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do.
- Integrity, Fairness, Honesty, and Perseverance
- and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people's lives
- including your own.
S and Puerto Rico positions:
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