Lab Quality Coordinator - 2nd Shift
Company: Biolife Plasma Services
Location: Monroe
Posted on: June 26, 2025
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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 Us: 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 centers and most importantly our commitment to our patients
is expected. BioLife Plasma Services is a subsidiary of Takeda
Pharmaceutical Company Ltd. What Takeda can offer you: 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. 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 bring Better Health and a
Brighter Future to people around the world. Role Overview:
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 (CLIA), and applicable Takeda and BioLife
policies, procedures and quality initiatives. Performs quality
assurance activities of BioLife Testing laboratory by performing
the following duties. ACCOUNTABILITIES Reviews testing, quality
control, and other testing reports for accuracy, completeness and
compliance to cGMP requirements to ensure that quality assurance
standards and regulatory requirements are met prior to release from
the Quality Assurance Department. Maintains familiarity with
laboratory operating and quality assurance/quality control
procedures and quality system processes in order to effectively
perform laboratory quality assurance functions. Adheres to the
laboratory quality control policies, document all quality control
activities, instrument and procedural calibrations and maintenance
performed. Identifies problems that may adversely affect test
performance or reporting of test results and either correct the
problems or immediately notify the laboratory management. 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 performance specifications.
Performs review and or validation of SOPs as needed. Participates
in operational excellence initiatives and projects to drive a
culture of continuous improvement to achieve site operational
excellence goals (including but not limited to 5S, Value Stream
Mapping, and Kaizen. Other duties as assigned. Technical/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 impact to product quality when testing deviations
occur, contain the situation and implement preventive actions.
Interaction Interfaces with employees of various educational
backgrounds and levels within the company. Must be able to
communicate effectively with all 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 performing 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 job.
EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS: 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 e
mployees 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, East Point , Lab Quality Coordinator - 2nd Shift, Science, Research & Development , Monroe, Georgia