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Quality Associate Ii Jobs in Kansas (NOW HIRING)

... data quality, standard operating procedures, or quality/compliance actions. The primary ... Associate II - (Maize, KS) are: * Ensure safe and efficient operation of the research program in ...

... data quality, standard operating procedures, or quality/compliance actions. The primary ... Associate II - (Maize, KS) are: * Ensure safe and efficient operation of the research program in ...

... data quality, standard operating procedures, or quality/compliance actions. The primary ... Associate II - (Maize, KS) are: Ensure safe and efficient operation of the research program in ...

... data quality, standard operating procedures, or quality/compliance actions. The primary ... Associate II - (Maize, KS) are: Ensure safe and efficient operation of the research program in ...

Field Associate II

Wichita, KS · On-site

$61.68 - $92.52/hr

Field Associate II The Field Associate II is a field‑facing role responsible for contributing to ... Ensure safe and efficient operation of the research program in alignment with Bayer's HSE, Quality ...

Join Adecco as a Production Associate II in Lenexa, KS, at a secure, climate-controlled facility ... Conduct accurate inspection, packaging, and labeling of products to meet quality standards.

Join Adecco as a Production Associate II in Lenexa, KS, at a secure, climate-controlled facility ... Conduct accurate inspection, packaging, and labeling of products to meet quality standards.

CRA II

Lawrence, KS · Remote

$91K - $114K/yr

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As ... Performing data review and resolution of queries to maintain high-quality clinical data.

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and ... You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ...

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Quality Associate Ii information

What is a quality associate ii?

Quality Associate IIs are professionals who work in quality assurance or quality control, typically within manufacturing, pharmaceuticals, or other regulated industries. They are responsible for ensuring products and processes meet established standards and regulatory requirements. Their duties may include inspecting materials, reviewing documentation, conducting audits, and collaborating with other departments to resolve quality issues. Quality Associate IIs often have more experience than entry-level associates and may assist in training or supervising junior staff. Their work helps maintain product safety, consistency, and compliance.

What are the key skills and qualifications needed to thrive as a quality associate ii?

To thrive as a Quality Associate II, you need a solid understanding of quality assurance processes, regulatory compliance, and technical documentation, often supported by a bachelor's degree in a scientific or technical field. Familiarity with quality management systems (QMS), statistical analysis tools, and industry-specific standards such as ISO or GMP is typically required. Strong attention to detail, analytical thinking, and effective communication skills set outstanding candidates apart. These abilities are crucial to ensuring product quality, regulatory adherence, and continuous process improvement in a highly regulated environment.

What are some typical challenges a quality associate ii might face when working on cross-departmental projects?

As a Quality Associate II, you may frequently collaborate with teams from production, engineering, and regulatory affairs. One common challenge is ensuring clear communication and alignment on quality standards across departments, especially when project timelines are tight or priorities differ. You’ll often need to balance attention to detail with efficiency, managing documentation and compliance tasks while supporting process improvements. Developing strong working relationships and proactive communication skills can help you address these challenges effectively and contribute to smoother project execution.

What is the difference between Quality Associate Ii vs Quality Control Technician?

AspectQuality Associate IIQuality Control Technician
Required CredentialsTypically an associate degree or higher in a related fieldOften an associate degree or technical certification
Work EnvironmentOffice and manufacturing settings, supporting quality processesLaboratory and production environments, performing testing and inspections
Employer & Industry UsageCommon in manufacturing, pharmaceuticals, and biotechPrimarily in manufacturing and production sectors
Search & Comparison IntentUnderstanding roles, responsibilities, and career pathFocus on testing procedures and technical skills

The main difference between a Quality Associate II and a Quality Control Technician lies in their focus and responsibilities. Quality Associate II roles often involve supporting quality systems, documentation, and process improvements, while Quality Control Technicians primarily perform testing and inspections to ensure product quality. Both roles require similar educational backgrounds but differ in daily tasks and work environments.

Is a Quality Associate II a good entry-level job?

A Quality Associate II role is typically considered an entry-level position in quality assurance or manufacturing environments, often requiring some prior experience or training. It involves tasks such as inspecting products, documenting quality issues, and using tools like inspection equipment, making it suitable for those starting their careers in quality control. However, the level of responsibility and required skills can vary by company.

What are popular job titles related to Quality Associate Ii jobs in Kansas?

For Quality Associate Ii jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Quality Associate Ii jobs in Kansas look for?

The top searched job categories for Quality Associate Ii jobs in Kansas are:

What cities in Kansas are hiring for Quality Associate Ii jobs?

Cities in Kansas with the most Quality Associate Ii job openings:

Infographic showing various Quality Associate Ii job openings in Kansas as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution.

Clinical Quality Control Associate II

Altasciences

Overland Park, KS • On-site

$65 - $90/hr

Other

Medical, Dental, Vision, Retirement, PTO

Re-posted 20 days ago


Altasciences rating

7.6

Company rating: 7.6 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

61st of 121 rated laboratories


Job description

Your New Company! At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences.

About The Role

The Clinical Quality Control Associate II is responsible for the quality control (QC) review of clinical trial data and working with the Quality Systems team to complete QC related tasks. The Clinical Quality Control Associate II will conduct

The Clinical Quality Control Associate II will conduct What You’ll Do Here within compliance of study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).

What You’ll Do Here
  • Ensure the confidentiality of clinical trial participants and sponsors is respected.
  • Maintain and advocate a high level of quality and customer service within the department.
  • Act as a mentor and coach the Quality Systems team members.
  • Record, track and ensure the resolution of data queries.
  • Assist in sponsor/regulatory audits.
  • May document and/or report clinical trial related deviations (i.e. SOP, protocol).
  • Identify and track error trends, report trends that may require re-training.
  • Compile data and maintain computerized files and/or update deviation tracking systems.
  • Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events.
  • Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
  • Complete and/or maintain training as required per jobs needs.
  • May provide departmental supervisors/managers with feedback for performance reviews.
  • Perform general administrative tasks when required.
What You’ll Need to Succeed
  • High School Diploma or GED and related work experience required; college degree and related work experience preferred.
  • Good communication, detail oriented, well organized, customer service focused, able to work in fast-paced environment.
What We Offer

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences' Benefits Package Includes:

Health/Dental/Vision Insurance Plans 401(k)/RRSP with Employer Match Paid Vacation and Holidays Paid Sick and Bereavement Leave Employee Assistance & Telehealth Programs

Altasciences' Incentive Programs Include:

Training & Development Programs Employee Referral Bonus Program Annual Performance Review #LI-JR1

MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH

Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request.

Join us at Altasciences!

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