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Bioanalytical Qa Jobs (NOW HIRING)

KCAS Bio

Director of Quality Assurance

Kansas City, KS · On-site

When you work as a Director of Quality Assurance at KCAS Bio, you have the opportunity to further ... Maintain expert knowledge of bioanalytical scientific trends as well as regulatory requirements

KCAS Bio

QA Specialist I

Kansas City, KS · On-site

Our Quality Assurance team partners closely with scientific and operational teams to maintain the quality, integrity, and compliance of the bioanalytical work performed at KCAS. As a Quality ...

KCAS Bio

QA Specialist I

Kansas City, KS · On-site

Our Quality Assurance team partners closely with scientific and operational teams to maintain the quality, integrity, and compliance of the bioanalytical work performed at KCAS. As a Quality ...

KCAS Bio

QA Specialist I

Kansas City, MO · On-site

Our Quality Assurance team partners closely with scientific and operational teams to maintain the quality, integrity, and compliance of the bioanalytical work performed at KCAS. As a Quality ...

Kcas, Llc

QA Specialist I

Kansas City, KS · On-site

Our Quality Assurance team partners closely with scientific and operational teams to maintain the quality, integrity, and compliance of the bioanalytical work performed at KCAS. As a Quality ...

Kcas, Llc

Our Quality Assurance team partners closely with scientific and operational teams to maintain the quality, integrity, and compliance of the bioanalytical work performed at KCAS. As a Quality ...

Altasciences

Senior QA Auditor

Columbia, MO · On-site

Autonomously performs SOP QA review, client hosting, regulatory agency hosting and external test site/clinical site/bioanalytical laboratory qualifications. Under supervision of a mentor/coach ...

New

Altasciences

Senior QA Auditor

Everett, WA · On-site

$80K - $87K/yr

Autonomously performs SOP QA review, client hosting, regulatory agency hosting and external test site/clinical site/bioanalytical laboratory qualifications. * Under supervision of a mentor/coach ...

Frontage Laboratories

QC Manager

Exton, PA · On-site

Collaborate with PI/RS, Bioanalytical Scientists, and QA to address errors, deviations. * Support on the data and documentation review for the CAP/CLIA assays handled by biomarker and biologics team.

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Bioanalytical Qa information

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How much do bioanalytical qa jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for bioanalytical qa in the United States is $44.87, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $54.57 per hour, depending on experience, location, and employer.

What is a bioanalytical QA?

A Bioanalytical QA (Quality Assurance) professional is responsible for ensuring the accuracy, reliability, and compliance of bioanalytical studies, which test biological samples for drugs, metabolites, or biomarkers. They review and audit laboratory data, processes, and documentation to ensure adherence to regulatory guidelines such as Good Laboratory Practice (GLP) and Good Clinical Practice (GCP). Bioanalytical QA specialists play a key role in maintaining data integrity, preparing for inspections, and supporting continuous improvement in laboratory environments.

What are the key skills and qualifications needed to thrive as a bioanalytical QA, and why are they important?

To thrive as a Bioanalytical QA, you need a solid understanding of bioanalytical methods, regulatory compliance, and quality assurance principles, often supported by a degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP), and regulatory guidelines such as FDA or EMA is essential. Attention to detail, strong problem-solving abilities, and effective communication skills help ensure data integrity and smooth collaboration within cross-functional teams. These skills and qualities are crucial for maintaining high standards of data quality and regulatory compliance in bioanalytical environments.

What are some common challenges faced by bioanalytical QA professionals and how can they be addressed?

Bioanalytical QA professionals often encounter challenges such as ensuring compliance with evolving regulatory standards, managing large volumes of complex data, and maintaining clear communication between laboratory and regulatory teams. To address these issues, it's important to stay updated on current guidelines (such as GLP and GCP), implement robust data management systems, and foster a culture of open collaboration. Proactively engaging in ongoing training and cross-functional meetings can also help address compliance and communication challenges.

What are popular job titles related to Bioanalytical Qa jobs?

For Bioanalytical Qa jobs, the most frequently searched job titles are:

Infographic showing various Bioanalytical Qa job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 90% Full Time, 3% Part Time, 4% Contract, and 1% Nights. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $93,338 per year, or $44.9 per hour.

Director of Quality Assurance

Kansas City, KS • On-site

KCAS Bio
See more jobs at KCAS Bioexternal

Full-time

Medical, PTO

Re-posted 10 days ago

Job description

Performing critical work that impacts our industry and our world's health while problem solving and innovating in the field - that is what the Director of Quality Assurance at KCAS Bio gets to do every day. If that gets you excited too, then maybe working as the Director of Quality Assurance is the role for you.

When you work as a Director of Quality Assurance at KCAS Bio, you have the opportunity to further our mission at the core by managing one or more QA departments or groups staffed by professional employees performing quality assurance functions and interacting with executive management, clients, and regulatory agencies as needed regarding quality systems, audits, and inspections.
 
You will be responsible for maintaining a high-level of professional expertise and leading regulatory inspections during FDA and critical client audits, overseeing the quality management system maintained at KCAS Bio, and providing expertise and guidance to all departments for interpreting and implementing health agency regulatory requirements.
 
While managing these responsibilities, you will also oversee the quality management system currently supported at KCAS Bio, meet department goals and objectives, and serve as a member of the Senior Leadership Team.
In this role, we will rely on you to:
  • Assure Quality systems are designed and performing to meet industry, regulatory and executive management requirements
  • Initiate employee hire, promotion, discharge, or transfer
  • Participate in the selection process for subordinate personnel including determining recruiting criteria, interviewing, and performing reference checks
  • Perform annual performance evaluations for direct reports
  • Require and monitor training for subordinates to develop them to their potential
  • Effectively use delegation to develop subordinates
  • Perform career planning for subordinates
  • Provide encouragement and positive reinforcement to subordinates; require subordinate leadership staff to do the same
  • Participate in the development of short and long-range goals and objectives, implement and attain short and long-range goals and objectives, and assure that year-end goals are attained
  • Assure that all departmental management staff are working in concert with each other
  • Coordinate activities of the department with related activities of other departments, to ensure efficiency and economy
  • Understand, communicate and cascade communication from Executive management
  • Be knowledgeable of site departmental budget and will monitor and analyze cost against budget
  • Overall responsibility for the Quality Assurance operation, compliance and site department goals including budget management
  • Interact with clients relating to quality audits, respond to client audit reports, and understand client needs/expectations
  • Complete client QA questionnaires and respective QA-assigned sections of RFIs
  • Forecast, recommend and justify strategies to accommodate growth when needed (space, equipment, staffing)
  • Establish policies and procedures to ensure that QA operations maintain a high level of QA expertise, remain abreast of current technologies and comply with related regulatory policies, OSHA and company SOPs/policies
  • Audit reports, data, internal processes, computer system validations, facility, and procedures to support management to improve data integrity, reduce error rates, efficiency, and maintain compliance
  • Manage internal auditing program including planning, conducting and reporting of audits
  • Conduct annual management review of the quality system
  • Manage digital quality systems, including eQMS administration, archiving, and related scanning
  • Ensure appropriate validation of methodology and instrumentation per regulatory requirement/industry expectation
  • Oversee CAPA system to ensure effective continuous improvement. Designates a CAPA
  • Coordinator and back-up within the department
  • Perform and track vendor quality assessments
  • Review/update SOPs to reflect current practice and regulatory requirements
  • Maintain expert knowledge of bioanalytical scientific trends as well as regulatory requirements
  • Perform complex quality assignments with understanding of underlying scientific principles
  • Recommend and institute systems and programs to improve safety, work quality, cost saving and productivity
  • Effectively interface with various functional units, groups or departments in the company
  •  
To qualify specifically for this role, you will have:
  • Bachelor's degree in a related field
  • Director-level experience preferred
  • 10 years industry-related experience, including 2 years supervisory experience
  • Experience in a CRO or pharmaceutical company is required
  • 3 to 5 years of GLP-regulated experience is preferred. GCP or GCLP are also acceptable.
  • Broad knowledge of regulatory requirements applicable to areas managed
  • Extensive knowledge of processes applicable to subordinate groups
  • Awareness of industry trends related to areas managed
  • Computer proficiency
  • Perform all aspects of the job in a way that supports the company brand and the company mission, vision, and values
(Please note this is a representative summary of responsibilities, not a comprehensive or exclusive list of the duties to be performed in any position. Employees must follow instructions and perform additional duties as requested.)
 
WHO YOU ARE
You will thrive at KCAS Bio if you enjoy a relational environment, are purpose- and values-driven, embrace constant development and supportive leadership, and enjoy being part of innovative work.
 
WHAT YOU'LL GET
Our benefits include, and extend beyond, the traditional package. At KCAS Bio, you will enjoy company sponsored events like food trucks, family days and spirit days. You will grow in your career with KCAS University. You will be able to connect with like-minded employees to further KCAS Bio's approach to key areas such as wellness, inclusion, and community outreach. You will engage as an owner in our stock ownership program. You will have access to the latest technology. And you will be able to invest in the community with paid time off to volunteer.
 
Learn more about the Benefits at KCAS Bio 
 
WHO WE ARE
We are a fast-growing contract research organization (CRO) headquartered in Kansas City, pioneering the latest drug development in both human and animal health fields. Demand for our expertise is growing and so is our need for great people to work in nimble, empowered teams committed to one another's growth. At KCAS Bio, we advance both great science AND great people.
 
Learn more about what it is like to work at KCAS Bio
 
KCAS Bio is proud to be an Equal Opportunity Employer. Among other things, we provide equal employment opportunities without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, sex, sexual orientation, gender identity, or any other legally protected category; we recruit qualified candidates without regard to citizenship status based on internal processes that enable us to hire the right candidates consistent with the appropriate U.S. Immigration framework; and (3) we work with and provide reasonable accommodations to individuals with disabilities and for sincerely held religious beliefs, observances, and practices. Anyone who needs reasonable accommodation may send an email to [email protected] or call 913-248-3000 (for TTY assistance call 711) and ask for Human Resources.
 
IND123
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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