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Gmp Quality Control Jobs in Colorado (NOW HIRING)

Probi LLC

Quality Manager

Lafayette, CO · On-site

$95 - $135/hr

POSITION SUMMARY The Quality Manager leads the Quality Assurance and Quality Control function in ... Identify and document risks and gaps applicable regulatory, GMP, GLP, ISO, and/or customer ...

Probi AB

Quality Manager

Lafayette, CO · On-site

$105K - $130K/yr

POSITION SUMMARY The Quality Manager leads the Quality Assurance and Quality Control function in ... Identify and document risks and gaps applicable regulatory, GMP, GLP, ISO, and/or customer ...

Probi

Quality Manager

Lafayette, CO · On-site

POSITION SUMMARY The Quality Manager leads the Quality Assurance and Quality Control function in ... Identify and document risks and gaps applicable regulatory, GMP, GLP, ISO, and/or customer ...

Probi

Quality Manager

Lafayette, CO · On-site

POSITION SUMMARY The Quality Manager leads the Quality Assurance and Quality Control function in ... Identify and document risks and gaps applicable regulatory, GMP, GLP, ISO, and/or customer ...

Actalent

Quality Lab Technician

Parker, CO

$20.50 - $25.75/hr

Strong knowledge of quality control principles, including performing assays, analytical testing ... Working knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) in a ...

New

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Gmp Quality Control information

What is the difference between Gmp Quality Control vs Gmp Quality Assurance?

AspectGmp Quality ControlGmp Quality Assurance
Primary FocusTesting and inspecting products to ensure compliance with standardsDeveloping and maintaining quality systems and processes
ResponsibilitiesSampling, testing, and documenting product qualityAuditing, process validation, and quality system oversight
CertificationsGMP training, laboratory skillsGMP knowledge, quality management system training
Work EnvironmentLaboratories, manufacturing sitesQuality departments, compliance offices

Gmp Quality Control focuses on testing products to verify they meet quality standards, while Gmp Quality Assurance involves establishing and maintaining systems to prevent defects. Both roles are essential in ensuring product safety and compliance in the pharmaceutical and biotech industries.

Is GMP Quality Control a good career path?

GMP Quality Control involves testing and inspecting pharmaceutical products to ensure they meet regulatory standards, making it a stable career with demand in the healthcare and biotech industries. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training or laboratory skills. The role offers opportunities for advancement into quality assurance, compliance, or management positions.

Is GMP Quality Control a good career?

GMP Quality Control is a stable career in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards. It involves tasks such as testing, documentation, and compliance, often requiring knowledge of laboratory techniques and certifications like GMP training. The role offers opportunities for advancement and consistent employment due to industry regulation requirements.

What is the role of quality control in GMP?

In GMP, quality control (QC) is responsible for testing and inspecting raw materials, in-process samples, and finished products to ensure they meet specified quality standards. QC helps prevent defective or unsafe products from reaching consumers by verifying compliance with regulatory requirements and maintaining proper documentation. QC professionals often use analytical tools and follow strict protocols to support product safety and efficacy.

What are popular job titles related to Gmp Quality Control jobs in Colorado?

For Gmp Quality Control jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Gmp Quality Control jobs in Colorado look for?

The top searched job categories for Gmp Quality Control jobs in Colorado are:

Gmp Quality Control jobs near you
Infographic showing various Gmp Quality Control job openings in Colorado as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Associate Director, Global Quality - API

CordenPharma

Boulder, CO • On-site

$150 - $170/hr

Other

Medical, Vision, Life, Retirement

Posted 6 days ago

Key responsibilities

  • Support sites in GMP compliance, quality systems, and operational challenges related to API manufacturing.

  • Assist with inspection readiness, audits, and remediation activities across the global API network.

  • Provide expertise on quality topics, monitor KPIs, and drive continuous improvement of quality systems.

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Associate Director, Global Quality - API

Regular Full-Time Management Boulder, CO, US

$150,000.00 To $170,000.00 Annually

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.

This role may be based in either Boulder, CO or N. Augusta, GA

SUMMARY

In this role, you act as a Global Quality Subject Matter Expert (SME) for API manufacturing, supporting sites across the network in GMP compliance, quality systems, and complex operational challenges. You work closely with local and global teams to ensure inspection readiness, robust processes, and consistent quality standards, while contributing hands-on to global quality initiatives and continuous improvement.

What makes this role relevant:

  • Strong expert role with global exposure across API sites
  • High impact on compliance, inspections, and quality systems
  • Focus on hands-on support, problem-solving, and continuous improvement
ESSENTIALDUTIESAND RESPONSIBILITIES

Include the following. Other duties may be assigned.

Expert / Advisory (Focus)

  • Act as SME for API GMP compliance (EU & FDA) across the global network
  • Support sites on complex quality topics, audits, and regulatory expectations
  • Provide expertise on quality systems, process robustness, and QbD principles
  • Advise on and execute quality integration activities (e.g. new sites, acquisitions)
  • Deliver training and guidance on GMP standards and best practices
  • Create and implement Corporate Compliance Standards.

Operational

  • Support inspection readiness, audits, and remediation activities
  • Monitor KPIs and identify risks, driving appropriate corrective actions
  • Participate in quality escalations and ensure structured investigations & CAPAs
  • Collaborate with sites on quality agreements and customer interactions
  • Drive harmonization and continuous improvement of quality systems across sites
EDUCATION and/or EXPERIENCE

BA or BS (scientific degree preferred) in Chemistry, Pharmacy, Engineering or related field from a four-year university; and 15 years’ experience in API quality, manufacturing or QA/QC; or equivalent combination of education and experience. Strong Quality background and experience is a must

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 expertise in EU GMP & FDA regulations
  • Hands-on experience with inspections, audits, and global quality systems
  • Proven track record as SME in API or CDMO environment
  • Strong stakeholder management and ability to work cross-functionally in global teams
  • Willingness to travel internationally (~40%)

SALARY

Actual pay will be based on your skills and experience.

BENEFITS

  • 401(k) matching - CordenPharma will contribute 100% of the first 6% - 100% vested after 2 years of service
  • Critical Illness Insurance
  • Disability Insurance
  • Employee Assistance Program
  • Flexible Spending Account
  • Health Insurance PPO/HSA
  • Hospital Indemnity Plan
  • ID Theft Protection
  • Life Insurance
  • Tuition Reimbursement
  • Wellness Program
  • 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.

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