1

Quality Control Analyst Per Diem Jobs in Colorado

Overview Physical Therapist - Per Diem - Denver, Colorado Join our world-class team of driven ... Ability to maintain quality, safety, and/or infection control standards. Responsibilities Provides ...

Overview Occupational Therapist - Per Diem - Denver, Colorado At Central Park Rehabilitation ... Ability to maintain quality, safety, and/or infection control standards. Responsibilities Evaluates ...

Overview Physical Therapist - Per Diem - Denver, Colorado Join our world-class team of driven ... Ability to maintain quality, safety, and/or infection control standards. Responsibilities Provides ...

Oversees the process for laboratory analysis of raw materials, in-process QC, finished goods release testing, and reserve sample management. * Participates in internal/external audits and regulatory ...

Overview Occupational Therapist - Per Diem - Denver, Colorado At Central Park Rehabilitation ... Ability to maintain quality, safety, and/or infection control standards. Responsibilities Evaluates ...

Oversees the process for laboratory analysis of raw materials, in-process QC, finished goods release testing, and reserve sample management. * Participates in internal/external audits and regulatory ...

As a Quality Control Specialist, you're the last line of defense between our precision microscopes ... Conduct warranty investigations and root cause analyses to identify failure trends, implement ...

... analytical procedures and methods, and regular monitoring, trending, and reporting of QC data to ... support product quality and continuous improvement. Activities • Perform daily control sampling ...

As a Quality Control Specialist, you're the last line of defense between our precision microscopes ... Conduct warranty investigations and root cause analyses to identify failure trends, implement ...

As a Quality Control Specialist, you're the last line of defense between our precision microscopes ... Conduct warranty investigations and root cause analyses to identify failure trends, implement ...

Analyze QC trends, identify deviations, and escalate issues as needed. Participate in root cause investigations and implement corrective/preventive actions (CAPAs). * Maintain accurate and complete ...

Showing results 21-40

Quality Control Analyst Per Diem information

What is a quality control analyst per diem?

Quality Control Analyst Per Diem jobs are positions where professionals are responsible for testing and ensuring the quality of products, typically in industries like pharmaceuticals, food, or manufacturing, but work on an as-needed or temporary basis. 'Per diem' means 'per day,' so these analysts are usually hired to fill in for regular staff, handle increased workloads, or assist with special projects. Their primary duties include sampling, testing materials, documenting results, and ensuring compliance with regulatory standards. Per diem roles offer flexibility but may not guarantee regular hours or benefits.

What does a quality control analyst per diem do?

As a Quality Control Analyst Per Diem, you are responsible for performing laboratory tests on raw materials, in-process samples, and finished products to ensure compliance with regulatory and company standards. Your work typically includes documenting results, identifying deviations, and communicating findings to production and quality assurance teams. Since this is a per diem position, you may be called upon to support peak workloads or cover for absent staff, requiring flexibility and adaptability. Your contributions are crucial in maintaining product integrity, minimizing recalls, and ensuring customer safety. Collaboration with other departments, such as manufacturing and R&D, is common to address and resolve quality issues efficiently.

What skills and qualifications are needed to thrive as a quality control analyst per diem?

To thrive as a Quality Control Analyst Per Diem, you need a solid understanding of laboratory testing, analytical techniques, and quality assurance principles, generally supported by a bachelor's degree in a scientific field. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or GC is typically required. Strong attention to detail, problem-solving skills, and effective communication are essential soft skills in this role. These competencies ensure that products meet strict quality standards and regulatory requirements, which is vital for consumer safety and organizational compliance.

What is the difference between Quality Control Analyst Per Diem vs Quality Control Analyst?

AspectQuality Control Analyst Per DiemQuality Control Analyst
Work ScheduleTemporary, on-call, or daily assignmentsFull-time, permanent position
CertificationsTypically requires industry certifications (e.g., GMP, GLP)Same certifications as Per Diem role
Work EnvironmentLaboratory or manufacturing settings, often in multiple locationsConsistent workplace, often in a single facility
Employment TypePer diem, often with flexible hoursFull-time employment with benefits

Both roles require similar credentials and work in laboratory or manufacturing environments. The key difference is that Per Diem positions are temporary and flexible, while full-time roles offer stability and benefits.

What are the most commonly searched types of Quality Control Analyst jobs in Colorado?

The most popular types of Quality Control Analyst jobs in Colorado are:

What are popular job titles related to Quality Control Analyst Per Diem jobs in Colorado?

For Quality Control Analyst Per Diem jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Quality Control Analyst Per Diem jobs in Colorado look for?

The top searched job categories for Quality Control Analyst Per Diem jobs in Colorado are:

What cities in Colorado are hiring for Quality Control Analyst Per Diem jobs?

Cities in Colorado with the most Quality Control Analyst Per Diem job openings:

QC Analyst II (Onsite) - 3rd Shift (Tuesday - Saturday)

Tolmar Inc.

Windsor, CO • On-site

$23.75 - $32/hr

Full-time

Re-posted 15 days ago


Tolmar rating

9.8

Company rating: 9.8 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

1st of 86 rated pharmaceutical


Job description

Core Hours: Tuesday - Saturday, 10:30 pm - 7:00 am

  • Training Hours may vary

Purpose and Scope

Performs routine testing of raw materials, cleaning samples, bulk intermediate and finished product, and/or stability samples, according to established regulatory protocols and procedures.

 Essential Duties & Responsibilities

  • Perform analyses on a variety of samples using intermediate preparation techniques and analysis methods. Employee will be trained and become proficient in the intermediate preparation techniques and analysis methods.
  • At the direction of management, train junior analysts in analysis methods and lab techniques.
  • Accountable for documenting all activities and maintaining records according to good documentation practices.
  • Accountable for proper use, care and maintenance of instrumentation.
  • Perform intermediate method transfers.
  • Provide detailed accounts of testing performed to investigators. Under the direct supervision of an investigator, may perform investigational testing.
  • Make scientific recommendations to management/technical writers regarding QC procedures.
  • Completes tasks on time and works to eliminate repeat errors. Follows all procedures applicable to job functions to ensure high quality of work.
  • Prioritizes tasks and performs job duties with minimal guidance from management. Works to complete tasks in an efficient manner, and is a productive member of the department. Contributes to a highly productive environment by avoiding distractions.
  • Employee is responsible for ensuring that company and regulatory data integrity guidelines are consistently followed.
  • Accountable for maintaining an atmosphere of teamwork, cordiality and respect towards co-workers. Willing to assist co-workers in the completion of tasks.
  • Will represent the department by providing accounts and results of method transfer activities and assist with troubleshooting aberrant method transfer results, if necessary.
  • Interacts respectfully with all other employees both inside and outside of the department and members of management, and shows interest in others' input and reasoning. Appropriately resolves differences of opinion.
  • Upon delegation, may be responsible for representing the QC chemistry laboratory when communicating with outside departments and vendors.
  • Identifies issues and escalates those issues to the department senior leadership or management as appropriate.
  • Provide support to the department leadership with the implementation of new systems, and continuous improvement efforts. Generates new ideas to create efficiencies and improve processes; willingly supports new ideas and process enhancements. 
  • Participate in required annual hazardous waste training. Hazardous waste involvement may include, but is not limited to container and tank management and inspections, generation of hazardous waste as a part of production or sampling processes and transfer of hazardous waste between lab procedure area, satellite accumulation and storage. Respond to spills per the Chemical Spill Procedures. 
  • Perform additional duties as assigned.

      Knowledge, Skills & Abilities

      • Knowledge of a government regulated laboratory environment, preferably for drugs or medical devices including cGMP, GLP and ICH and their application to laboratory testing and review processes and procedures.
      • Intermediate understanding of the use of USP, NF and other compendia.
      • Ability to use and maintain analytical laboratory instruments such as HPLC, FTIR, GPC, GC, and UV-Vis spectrophotometers.
      • Effective written and oral communication skills.
      • Knowledge of computer systems for sample tracking, laboratory equipment, raw data handling and storage.
      • Ability to interpret, understand and follow analytical procedures/calculations and scientific principles.

      Core Values

      • The QC Analyst II 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 and treat 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 with an enterprise‑wide mindset that lifts the whole organization.
        • 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 proactive, collaborative effort to enhance our products, systems, processes, and services by reducing waste, increasing efficiency, and improving quality. We strive to be innovative, embracing calculated risk‑taking that drives better ways of working.
        • 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

      • Bachelor’s degree in scientific discipline, preferably in Chemistry or Biochemistry.
      • Two or more years of experience in an analytical laboratory position.

      Compensation and Benefits

      • Pay: $36.00 - $37.00 per hour, depending on experience
      • Shift Differential: 20% after training period
      • Benefits summary:  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. 

      Working Conditions

      • Laboratory setting. Will be exposed to solvents, bio-hazardous materials, hazardous waste, and pharmaceuticals.
      • Must be adaptable to shifting priorities and operate with a sense of urgency while maintaining high quality in order to meet important timelines in a high throughput lab.
      • Business demands may present a need to work extended hours.

      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.


      What Tolmar employees say

      Pay

      Benefits

      Hours and flexibility

      Workplace

      Get the full story on Breakroom


      Tolmar logo

      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