Quality Coordinator - 2nd Shift

Company: Biolife Plasma Services
Location: Monroe
Posted on: February 16, 2026

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 BioLife Plasma Takeda offers a purpose you can believe in, a team you can count on, opportunities for career growth, and a comprehensive benefits program, all in a fast-paced, friendly environment. Every day at BioLife, we feel good knowing that what we do helps improve the lives of patients with rare diseases. While you focus on our donors, we'll support you. 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. We are certified as a Global Top Employer and offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace in which our teams are united by an unwavering commitment to bring Better Health and a Brighter Future to people around the world. Every day, our BioLife Testing Laboratories’ mission is to ensure the highest quality testing standards for the plasma we collect. The plasma our centers collect will become life-changing medicines for patients in need. Here, a commitment to lab testing quality, customer service to our plasma centers, and most importantly, our commitment to our patients is expected. BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. OBJECTIVES/PURPOSE Responsible for the operation of the laboratory In accordance with established Standard Operating Procedures (SOPs), applicable sections of the Code of Federal Regulations (CFRs), with emphasis on Good Manufacturing Practices (GMPs), the Clinical Laboratory Improvement Act of 1988 (CUA), and applicable Takeda and BioLife policies, procedures and quality initiatives. Performs Q uality A ssurance activities at the BioLife Testing L aboratory by performing the following duties. ACCOUNTABILITIES: Reviews testing, quality control, and other' testing reports for accuracy, completeness and compli ance to cGMP requirements to ensure that quality assurance standards and regulatory requirements are met prior to release from the Quality Assurance Department. (70%) Maintains familiarity with laboratory operating and quality assurance/quality control procedures and quality system processes in order to effectively perform laboratory quality assurance func tions. (5%) Adheres to the laboratory quality control policies, document all quality control activities, instru ment and procedural calibrations and maintenance performed. (5%) Identifies problems that may adversely affect test performance or reporting of test results and eit her correct the problems or immediately notify the laboratory management. (10%) Follow established corrective action policies and procedures whenever test systems are not within established acceptable levels of performance. Document all corrective actions taken when test systems deviate from established perfor mance specifications. Performs review and or validation of SOPs as needed. (5%) Participates in operational excellence initiatives and projects to drive a culture of continuous im provement to achieve site operational excellence goals (Including but not limited to 5S, Value Stream Mapping, and Kaizen. (5%) Other duties as assigned. DIMENSIONS AND ASPECTS: Technical and Functional Line Expertise: Strong knowledge and understanding of applicable regulatory and quality requirements and standards. Strong written, verbal, personal interaction and communication skills required. Must be able to write concisely and clearly. Attention to detail and organizational skills with analytical and problem solving skills. Proficiency in the use of personal computers and software programs including Microsoft Word, Excel and PowerPoint. Result oriented with ability to adapt to changing priorities. Leadership Integrity Fairness Honesty Perseverance Putting the patient at the center Building trust with society Reinforcing our reputation Developing the business Decision-Making and Autonomy Must be able to determine the impact to product quality when testing deviations occur, contain the situation and Implement preventive actions. lnteraction Interfaces with employees of various educational backgrounds and levels within the company. Must be able to communicate effectively with aH these various business partners. Complexity Ability to stand up for 6-8 hours Ability to lift, carry and pull up to twenty-five (25) pounds Walking, standing, observing others perfonning work assignments. Potential exposure to blood borne pathogens requires some work tasks to be performed while wearing gloves. Ability to work in an office / production environment. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions of this role. EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS: Essential: Bachelor's degree or higher from an accredited college/university in a biomedical discipline (Chemical, physical, biological, clinical lab science, or medical technology,) OR Associate degree from an accredited college/university in laboratory science or medical laboratory technology. Desired: Minimum of two years' experience in a professional or technical capacity in laboratory services, blood services, quality, or pharmaceutical manufacturing, Including significant exposure to the regulatory requirements affecting that discipline or activity. Technical/Professional certification preferred. Prior experience with auditing and/or inspection processes preferred. MT or MLT certification from ASCP or other accredited certifying organization preferred BioLife Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. W e 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 - Baxter Pkwy U.S. Hourly Wage Range: $18.85 - $29.62 The estimated hourly wage range reflects an anticipated range for this position. The actual hourly wage 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 hourly wage 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 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 - GA - Social Circle - Baxter Pkwy Worker Type Employee Worker Sub-Type Regular Time Type Full time Job Exempt No

Keywords: Biolife Plasma Services, Marietta , Quality Coordinator - 2nd Shift, Science, Research & Development , Monroe, Georgia