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Quality Control Associate Jobs in Saint Joseph, MO

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Quality Control Associate information

See Saint Joseph, MO salary details

$11

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$36

How much do quality control associate jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for quality control associate in Saint Joseph, MO is $24.61, according to ZipRecruiter salary data. Most workers in this role earn between $17.88 and $29.95 per hour, depending on experience, location, and employer.

What does a quality control associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

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

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges quality control associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

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

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

What are the most commonly searched types of Quality Control jobs in Saint Joseph, MO?

The most popular types of Quality Control jobs in Saint Joseph, MO are:

What cities near Saint Joseph, MO are hiring for Quality Control Associate jobs?

Cities near Saint Joseph, MO with the most Quality Control Associate job openings:

Infographic showing various Quality Control Associate job openings in Saint Joseph, MO as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $51,179 per year, or $24.6 per hour.

Quality Control Associate Scientist I - Environmental Monitoring

Catalent Pharma Solutions

Kansas City, MO • On-site

Full-time

Medical, Dental, Vision, Life, PTO

Posted 5 days ago


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

63rd of 86 rated pharmaceutical


Job description

About Site

Catalent's Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.

Position Summary

We have an opportunity for a Quality Control Associate Scientist I to join our team. In this role, you will perform tasks under close supervision, following detailed instructions and established procedures. You will apply your technical skills to complete assigned work within your group or project team. This position requires a self-motivated, detail-oriented individual who can make decisions, solve problems, and work independently while supporting team members as needed.

Shift: Monday to Friday 8am-4pm
Location: Kansas City, MO
100% Onsite

The Role

  • Collect environmental samples such as water, non-viable particulates, viable particulates, and compressed gasses on a routine basis and perform testing on these samples.

  • Identify results within alert or action limits and notify management as appropriate.

  • Execute laboratory work plans and schedules developed with input from a supervisor or senior team member.

  • Maintain high-quality documentation in accordance with regulatory guidance and site Standard Operating Procedures, recording work in notebooks, forms, and other required formats.

  • Execute procedures or methods of moderate complexity with accuracy and review own work for completeness, identifying minor quality or compliance gaps during lab work.

  • Draft technical documents such as methods or certificates of analysis under direct guidance from a supervisor or senior team member.

  • Perform peer review of routine laboratory documentation and review technical documents for accuracy and thoroughness.

  • Demonstrate laboratory techniques during training and provide shadowing for lab orientation.

  • Assist in efficiency and compliance improvement projects with guidance.

  • Perform all other duties as assigned.

The Candidate

Minimum Requirements

  • Associate's degree in a related life science or physical science field with 1+ years of relevant work experience required.

  • Strong mathematical and scientific reasoning ability with the capacity to learn and retain technical information.

  • Ability to proactively address work issues at an individual level.

  • Capable of interpreting a variety of instructions in written, oral, diagram, or schedule form.

  • Developing core techniques and skills and applying them to new areas of work.

  • Understanding of laboratory-related Good Manufacturing Practices expectations and concepts.

  • Ability to identify out-of-specification data and provide limited interpretation of data.

  • Excellent written and verbal communication skills with internal customers.

  • Able to communicate barriers to management when prompted.

  • Lead by example according to Catalent's values and culture.

  • Understand how daily activities impact the performance of the group, site, and business.

  • Act in the best interests of colleagues, patients, customers, and the organization.

  • Recognize unmet needs within the team.

  • Strong time management and organizational skills with the ability to multitask.

  • Ability to work effectively under pressure to meet deadlines.

  • Inclusive and values diverse perspectives.

  • Physical Requirements: Ability to walk, sit, and stand; use hands to handle or feel; reach with hands and arms at or above shoulder height and below waist height; climb or balance; stoop, kneel, crouch, or crawl; talk and hear; smell; and lift up to 40 pounds during an average 8-hour day.

  • Specific vision requirements include reading written documents, visual inspection of materials, and frequent use of a computer monitor.

  • May require the use of a respirator.

Preferred Skills & Background

  • Bachelor's degree in a related life science or physical science preferred.

Why You Should Join Catalent

  • Defined career path with annual performance reviews and feedback process.

  • Diverse and inclusive culture.

  • Potential for career growth on an expanding team within an organization dedicated to preserving and improving lives.

  • Competitive paid time off plus 8 paid holidays.

  • Community engagement and green initiatives.

  • Medical, dental, and vision benefits effective on day one of employment.

  • Tuition reimbursement.

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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