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Quality Lab Associate Jobs in Colorado (NOW HIRING)

Core Hours Monday - Friday, 8:00 am - 4:30 pm Purpose and Scope The Quality Control Associate I ... lab procedure area, satellite accumulation and storage. Respond to spills per the Chemical Spill ...

Core Hours Monday - Friday, 8:00 am - 4:30 pm Purpose and Scope The Quality Control Associate I ... lab procedure area, satellite accumulation and storage. Respond to spills per the Chemical Spill ...

Core Hours Monday - Friday, 8:00 am - 4:30 pm Purpose and Scope The Quality Control Associate I ... lab procedure area, satellite accumulation and storage. Respond to spills per the Chemical Spill ...

Onsite Lab Coordinator

Boulder, CO · On-site

$25 - $26/hr

Meeting established goals and objectives related to safety, performance, and quality. * Creating ... Join our global team of 14,000+ associates whose passion for discovery and determination to ...

Meeting established goals and objectives related to safety, performance, and quality. * Creating ... Join our global team of 14,000+ associates whose passion for discovery and determination to ...

Onsite Lab Coordinator

Boulder, CO · On-site

$25 - $26/hr

Meeting established goals and objectives related to safety, performance, and quality. * Creating ... Join our global team of 14,000+ associates whose passion for discovery and determination to ...

We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 ... Associates Degree in a Chemistry or similar scientific discipline and 1-2 years of years' relevant ...

Implement and monitor lab policies, procedures, and quality control standards * Support operating ... Completion of a two-year associate degree program in Medical Laboratory Technology or Bachelors of ...

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Showing results 1-20

Quality Lab Associate information

What are the key skills and qualifications needed to thrive as a Quality Lab Associate, and why are they important?

To thrive as a Quality Lab Associate, you need a solid background in laboratory procedures, analytical testing, and quality assurance, usually supported by a degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), analytical instruments like HPLC/GC, and relevant certifications such as GMP or ISO standards is often required. Attention to detail, strong organizational skills, and effective communication enable you to identify problems, maintain accurate records, and collaborate with cross-functional teams. These skills ensure the integrity of test results, regulatory compliance, and overall product quality in laboratory environments.

What are some common challenges Quality Lab Associates face when working with cross-functional teams?

Quality Lab Associates often collaborate with production, R&D, and regulatory teams to ensure product quality and compliance. A common challenge in this environment is effectively communicating technical laboratory findings to non-technical stakeholders, which requires clear documentation and presentation skills. Additionally, balancing multiple project deadlines while maintaining strict adherence to quality standards can be demanding. Building strong relationships and understanding the goals of other departments can help overcome these challenges and foster smoother workflows.

What does a Quality Lab Associate do?

A Quality Lab Associate is responsible for performing laboratory tests and analyses to ensure that products meet established quality standards and regulatory requirements. This role typically involves preparing samples, operating laboratory equipment, recording data, and reporting results to supervisors or quality managers. They may also assist in investigating deviations or non-conformities and help maintain a clean and safe laboratory environment. Quality Lab Associates play a critical role in maintaining product safety and consistency, particularly in industries like pharmaceuticals, food and beverage, or manufacturing.

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

AspectQuality Lab AssociateQuality Control Technician
CertificationsOften requires a degree in science or related field; certifications like ASQ are a plusSimilar requirements; certifications like ASQ are common
Work EnvironmentLaboratory setting, performing tests and analysesLaboratory and production environment, conducting inspections and tests
Employer & Industry UsageUsed across manufacturing, pharmaceuticals, food, and biotech industriesCommon in manufacturing, pharmaceuticals, and food industries

Both roles involve testing and ensuring product quality, often requiring similar educational backgrounds and certifications. The main difference lies in their focus: Quality Lab Associates typically perform routine testing and data recording, while Quality Control Technicians may also conduct inspections and troubleshoot quality issues on the production line.

What are the most commonly searched types of Quality Lab jobs in Colorado? The most popular types of Quality Lab jobs in Colorado are:
What cities in Colorado are hiring for Quality Lab Associate jobs? Cities in Colorado with the most Quality Lab Associate job openings:
QA Associate I - Process (3rd Shift)

QA Associate I - Process (3rd Shift)

Tolmar Inc.

Fort Collins, CO

$19.62/hr

Full-time

Posted 7 days ago


Job description

Core Hours

Sunday - Wednesday, 5:00 pm - 5:30 am, every other Wednesday off

Purpose and Scope

The Quality Assurance Associate I is responsible for the inspection, testing, record keeping and overall quality assurance support to manufacturing.

Essential Duties & Responsibilities

  • Inspect material, components, and finished product against specified requirements.
  • Follow procedures to determine status or disposition, and properly document results on records and in lab notebooks.
  • Support manufacturing and QC unit with inspections and material sampling.
  • Complete training according to requirements and maintain training records in the electronic document system.
  • Perform finished product inspections in accordance with specification; ensuring proper sampling has taken place prior to final release.
  • Provide process oversight support to manufacturing.
  • Ensure proper status and storage of materials and product.
  • Complete review and release of materials as required.
  • Provide quality oversight throughout multiple departments and facilities.
  • Initiate deviations and complete immediate actions.
  • Participate in monthly quality and safety walkthroughs.
  • Perform various other duties as assigned.

Knowledge, Skills & Abilities

  • Working knowledge in drug or device cGMP.
  • Knowledge of computer operations, including proficiency with MS Word, Excel and Access.
  • Ability to learn Tolmar’s electronic systems.
  • Skill in organization and attention to detail.
  • Skill in effective written and oral communication.
  • Work independently and properly prioritize tasks with limited supervision.
  • Ability to work well with employees at all levels and departments.
  • Ability to read, understand and follow procedures.
  • Demonstrate competency in technical writing.
  • Ability to use critical thinking to address potential areas of concern.

Core Values

  • The QA Associate I is expected to operate within the framework of Tolmar’s Core Values:
    • Center on People: We commit to support the well-being of our patients. We are committed to treating our employees and those we serve as valued partners. By placing people at the heart of our actions, we actively engage, invigorate, acquire knowledge, and grow together.
    • Are Proactive & Agile: We embody a culture of engagement and action. With a hands-on approach, we fearlessly adapt to change. We anticipate, respond swiftly and efficiently to ignite a spirit that propels us towards extraordinary outcomes.
    • Act Ethically: We are committed to consistently conducting our business in an ethical, compliant, and socially aware manner, in line with our purpose of positively impacting lives. We actively cultivate diversity, equity, inclusion & sustainability in our workplace.
    • Constantly Improve: We are committed to a collaborative & proactive effort to improve our products, systems, processes, and services by reducing waste, increasing efficiency & improving quality.
    • Are Accountable: We think, act, and communicate with honesty, transparency, and clarity in alignment with our core values. We don't compromise our values for near term gain. We take accountability & ownership of our work, actions, successes, and setbacks. We strive to deliver our best as we shape the future.

Education & Experience

  • High school diploma, GED, or equivalent required.
  • Associate’s degree preferred.
  • Experience in a high volume manufacturing environment preferred.
  • Experience in a Quality Assurance capacity in the pharmaceutical or medical device industry preferred.

Additional Requirements

  • Ability to bend, squat, and lift minimum of 30 pounds required.
  • Ability to pass physical and eye exam required. Ability see color.

Working Conditions

  • Working conditions are in an office, warehouse and manufacturing environment.
  • Occasional overtime may be required.
  • Work may consist of travel between multiple facilities.

Compensation and Benefits

  • Pay: $19.62 per hour
  • Shift Differential: $2.50 per hour
  • Benefits information: https://www.tolmar.com/careers/employee-benefits

Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidates qualifications and experience.

Tolmar is an Equal Opportunity Employer. We do not discriminate on the basis age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law. It is our intention that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors.


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About Tolmar

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Fort Collins, CO, US

Year founded

2006