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Would you like to develop your skills working for a mission-driven organization while playing an important role in leading the way in Life Sciences? AlloSource is a BioTech company headquartered in Centennial, Colorado. 

Here at AlloSource we're not looking for jobseekers. We want people dedicated to our mission of restoring hope to donor families and helping patients heal through our innovative cellular and tissue allografts. This takes a special person with a strong desire to help make a tremendous impact on people's lives. Regardless of which department you work in at AlloSource, we value your efforts, your top-notch skills, and your abilities to contribute to our ultimate goal of saving or enhancing human life! What better reward is there than knowing you contributed, in some way, to save or enhance a person's life! If this sounds like an organization you wish to be a part of, then we invite you to apply.

*Summary: *

The QA Laboratory Supervisor assist laboratory management with leading the Quality Assurance Laboratory with laboratory activities. The Supervisor will assist with managing and monitoring team responsibilities as it relates to daily laboratory work. This position is responsible for ensuring procedures are followed for respective QA laboratory activities. The Supervisor will model professional behavior, recommend appropriate staffing levels, communicate frequently, and work with multiple departments/cross-functional teams to support operations and achieve company goals.

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*Anticipated Application Deadline: February 4, 2026 *

Pay: $

72,419/yr.  - $88,501/yr. based upon years of relevant experience 

*Shift Differential: *

$233.33/month

*Shift: *  Monday-Thursday; 12;00pm to 10:30pm 

Benefits: *Medical, Dental, Vision, Life Insurance. Click link for more benefits details: View the 2026 Employee Benefits Summary{rel="noopener noreferrer" target="_blank"}                                                                              *

Location:

  6278 S Troy Circle Centennial, Colorado 80111 

*Essential Duties and Responsibilities: *

*Leadership *

• Assist senior laboratory management with managing and monitoring team activities for timeliness of completion of documentation, workload distribution, and project resourcing.
• Develop and report on departmental performance metrics and measure team execution with tracking and trending techniques. 
• Provide subject matter expertise with QAL team activities and responsibilities. 
• Build and lead a high-performing team by hiring, training, and developing staff. Foster a collaborative work environment and drive results through continuous coaching, mentoring, and performance management.

*QA Laboratory Operations *

• Oversee the utilization of the electronic systems to perform test ordering with third-party and the internal laboratory for QC test outputs, as well as creating the corresponding inspection plans.
• Lead and perform all elements of the quality control testing process, including sampling of preprocessing/intermediate/final product, and the corresponding environmental monitoring testing.
• Perform all elements of the Environmental Monitoring Program, including sampling of non-viable, viable air, personnel monitoring, settle plates, swabs, water, and special testing. 
• Perform microbial evaluation according to established procedures using appropriate laboratory techniques for accurate microorganism identification and interpretation of results. 
• Perform product-based QC testing, including both microbi logical and non-microbiological methods. 
• Execute appropriate quality control procedures and proper documentation to comply with regulatory agencies. 
• Participate in CLIA proficiency testing. 
• Perform timely testing and closure of environmental monitoring paperwork and reports. 
• Manage sterilization microbiological activities with assigned product line dose audits. 
• Manage sterilization of testing equipment utilizing in-house autoclaves.
• Own assay specifications. 
• Participate with internal, customer, and regulatory audits. 
• Oversee laboratory activities in cleanroom area.
• Manage equipment, including biological safety cabinet, autoclave, and testing equipment.

*Research & Validation Work *

• Manage and execute research activities with analytical techniques, written procedures, and standard protocols to support research, scientific, or technical-related disciplines. Perform specialty testing and research validation work.
• Complies with accurate experimental data entry into notebooks and computer databases 
• Interprets and analyzes scientific data into reports and summary documents.
• Manage and perform Method Suitability (B/F) projects and other laboratory studies.

*Aseptic Processing Program *

• Lead and interact in Aseptic Processing Program meetings, reviews, and project teams
• Lead with collating all required data trending information from group for Aseptic Processing Program and Management Review. 
• Perform QC data visualization analysis with designated product line(s).
• Run assigned process simulation activities with designated product line(s). 

*Communication *

• Professionally interact and communicate with internal and external customers/vendors, laboratories, and process stakeholders. 

*Improvement *

• Lead in the development, evaluation, and review of policies, procedures, and methodologies for the laboratory in order to maintain compliance with accreditation.   Adhere to and promote proper practices and techniques which are consistent with current operating procedures, training requirements, safety practices and company policies. 
• May perform other related duties and responsibilities as assigned.

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*Requirements: *

• Bachelor's degree in a technical, scientific or  Medical Technology related field
• 4+ years (w/ Bachelor's degree) in medical device, pharmaceutical, or related scientific environment or 1+ years (w/ Master's degree) in medical device, pharmaceutical, or related scientific environment 
• 3+ years of Microbiology laboratory experience 
• Quality Assurance/Regulatory Affairs experience in a manufacturing environment or other technical industry
• Proficiency in Microsoft Office applications 
• Ability to communicate in English proficiently (speaking, reading, writing, and comprehension 

*Preferred Experience *

• AATB Certification 
• ASQ Certifications 
• Master's degree in scientific field 
• 3+ years' supervisory experience
• Experience with Quality Management System software
• FDA & CLIA regulated environment experience
• Tissue banking experience 

• FDA/ISO/CLIA audit experience

   

*It is the policy of AlloSource not to discriminate against qualified individuals with disabilities in regard to application procedures, hiring, advancement, discharge, compensation, training or other terms, conditions and privileges of employment. If you need reasonable accommodation to apply for a position, please contact us at 720-873-0213. *

For consideration, you must apply online, submit a current resume and meet the minimum requirements. Candidates within a 50-mile radius of the hiring zip code may receive first consideration. 

*Equal Opportunity **Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identit