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Quality Control Analyst Per Diem Jobs in Colorado

QC Analyst

Boulder, CO ยท On-site

$31.65 - $39/hr

Analytical skills and knowledge of general or organic chemistry * Mechanical aptitude with lab equipment * Support Senior level QC staff with general lab duties * Preform basic methods on test ...

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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

Corden Pharma Colorado

Boulder, CO โ€ข On-site

$31.65 - $39/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 days ago


Job description


CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in active pharmaceutical ingredients (APIs), excipients, drug products (DPs), and packaging. With around 3,000 employees worldwide, we help pharmaceutical and biotech companies manufacture medicines with the ultimate goal of improving people’s lives.


Our network, spanning Europe and the U.S., provides flexible and specialized solutions across six technology platforms: Peptides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules, and Oligonucleotides. We strive for excellence in supporting this network and are committed to delivering the highest quality products for patient well-being.

 

OUR PEOPLE VISION

We strive for excellence. We share our passion. Together, we make a difference in patients' lives.


SUMMARY

Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training manual. Maintains a high level of housekeeping and attention to detail. 

ESSENTIAL DUTIES AND RESPONSIBILITIES

Include the following. Other duties may be assigned.

  • Run routine samples of raw materials, intermediates, and final products. Test special request samples from plants, tech center, or process chemists
  • Perform equipment calibration, titrant standardization, and standard validation as required
  • Identify and correct problems with instruments in QC lab. Identify and communicate problems and solutions related to process, procedure, and materials to QC Chemist. Researches and takes corrective action on anomalous test results
  • Maintain cleanliness and organization of lab by following safety, regulatory, and chemical hygiene policies including GLPs and GMPs
  • Perform daily record keeping on SAP and LIMS, enter status changes for raw materials, initiate incident reports, and issue approval-for-use tags
  • Responsible for properly managing the generation and accumulation of hazardous and non-hazardous waste
  • Attend and participate in QC Team meetings. Develop team skills
 LEADERSHIP & BUDGET RESPONSIBILITIES

None.

SAFETY & ENVIRONMENTAL RESPONSIBILITIES

Every individual is personally responsible for the safety and environmental aspects of his or her activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience.

QUALIFICATIONS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

EDUCATION and/or EXPERIENCE

Bachelor's Degree (BA) from 4-year college or university; or 1 year of related experience and/or training; or equivalent combination of education and experience. GMP and lab equipment experience preferred.

LANGUAGE SKILLS

Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of the organization.

MATHEMATICAL SKILLS

Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume. Ability to apply concepts of basic algebra and geometry.

REASONING ABILITY

Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

CERTIFICATES, LICENSES, REGISTRATIONS

None.

PHYSICAL DEMANDS

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is regularly required to work with hands and talk or hear. The employee frequently is required to stand, walk, and sit. The employee is occasionally required to reach above shoulder height; climb or balance; stoop, kneel, crouch, or crawl; and taste or smell. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus.

WORK ENVIRONMENT

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles, low levels of toxic or caustic chemicals, and outside weather conditions. The noise level in the work environment is usually moderate.

CORE COMPETENCIES

These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity.

  • Strong math, reading, and comprehension skills
  • Analytical skills and knowledge of general or organic chemistry
  • Mechanical aptitude with lab equipment
  • Support Senior level QC staff with general lab duties
  • Preform basic methods on test samples
  • Good communication skills and computer skills
  • Commitment to QEH&S Principles
  • Ability to work closely with team members to a common goal
  • Attention to detail
  • Ability to work on 12 hour rotating shifts, night or day; weekends and holidays required
SALARY

Actual pay will be based on your skills and experience.

 BENEFITS
  • 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service 
  • Accident Plan
  • Critical Illness Insurance
  • Dental Insurance
  • Disability Insurance
  • Employee Assistance Program
  • Flexible Spending Account
  • Health Insurance PPO/HSA
  • Hospital Indemnity Plan
  • ID Theft Protection
  • Life Insurance
  • Paid Parental Leave
  • Tuition Reimbursement
  • Wellness Program
  • Vacation – Three Weeks 1st Year
  • Vision Insurance
EQUAL OPPORTUNITY EMPLOYER

Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices.


This post will expire June 12, 2026