BioLife Plasma Services
Quality Lead Tech - Sign On Bonus Eligible!
BioLife Plasma Services, Dubuque, Iowa, United States, 52001
Quality Lead Tech – Sign On Bonus Eligible!
Join BioLife Plasma Services as the Quality Lead Tech and help improve the lives of patients with rare diseases.
Job Description $1500 Sign On Bonus Eligible
About BioLife Plasma Services Every day at BioLife, we help improve lives. We offer purpose, a reliable team, career growth, and comprehensive benefits in a fast‑paced, friendly environment.
Objectives / Purpose Monitors designated systems and activities to ensure consistent source plasma manufacturing in accordance with cGMP, Shire Quality System, and applicable regulations.
Accountabilities
Reviews operational records and ensures they are complete, accurate, and compliant with cGMP.
Tracks deviations, reports deficiencies, and observations to center management and QMR.
Conducts monthly quality assurance audits for critical control points.
Ensures SOPs are current and staff perform routine tasks per SOP.
Prepares for and hosts internal auditors and external inspectors when needed.
Maintains qualifications and performs duties in Medical History, Phlebotomy, and Sample Processing.
Provides leadership and training assistance to center management and supervisory team.
Skills, Education, & Competencies
Minimum 1 year relevant experience or equivalent education.
Certification in Medical History, Phlebotomy, and Processing Technician.
Completion of all Lead Technician training.
Demonstrated knowledge of FDA‑regulated quality assurance.
Effective communication, organizational, and problem‑solving skills.
Leadership qualities, integrity, fairness, and honesty.
Ability to read and follow SOPs and maintain accurate records.
Other Duties & Responsibilities Works collaboratively to continuously improve processes using 5S, Value Stream Mapping, and Kaizen. Supports center management in identifying opportunities for operational improvement.
Benefits & Compensation Hourly Rate:
$19.00 – $24.75 (dependent on experience & location) Access to medical, dental, vision, 401(k) plan with company match, disability coverage, paid vacation and sick time, tuition reimbursement, and volunteer time off.
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.
Location & Employment Type USA – IA – Dubuque Full‑time, non‑exempt, regular employee, full‑time job, entry level, quality assurance role.
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Job Description $1500 Sign On Bonus Eligible
About BioLife Plasma Services Every day at BioLife, we help improve lives. We offer purpose, a reliable team, career growth, and comprehensive benefits in a fast‑paced, friendly environment.
Objectives / Purpose Monitors designated systems and activities to ensure consistent source plasma manufacturing in accordance with cGMP, Shire Quality System, and applicable regulations.
Accountabilities
Reviews operational records and ensures they are complete, accurate, and compliant with cGMP.
Tracks deviations, reports deficiencies, and observations to center management and QMR.
Conducts monthly quality assurance audits for critical control points.
Ensures SOPs are current and staff perform routine tasks per SOP.
Prepares for and hosts internal auditors and external inspectors when needed.
Maintains qualifications and performs duties in Medical History, Phlebotomy, and Sample Processing.
Provides leadership and training assistance to center management and supervisory team.
Skills, Education, & Competencies
Minimum 1 year relevant experience or equivalent education.
Certification in Medical History, Phlebotomy, and Processing Technician.
Completion of all Lead Technician training.
Demonstrated knowledge of FDA‑regulated quality assurance.
Effective communication, organizational, and problem‑solving skills.
Leadership qualities, integrity, fairness, and honesty.
Ability to read and follow SOPs and maintain accurate records.
Other Duties & Responsibilities Works collaboratively to continuously improve processes using 5S, Value Stream Mapping, and Kaizen. Supports center management in identifying opportunities for operational improvement.
Benefits & Compensation Hourly Rate:
$19.00 – $24.75 (dependent on experience & location) Access to medical, dental, vision, 401(k) plan with company match, disability coverage, paid vacation and sick time, tuition reimbursement, and volunteer time off.
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.
Location & Employment Type USA – IA – Dubuque Full‑time, non‑exempt, regular employee, full‑time job, entry level, quality assurance role.
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