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Pharmaceutical Engineering Jobs in Colorado (NOW HIRING)

JLL

Global Technical Engineering Lead

Boulder, CO · On-site

As Global Technical Engineering Lead, you will delight our Life Sciences client through the ... Lead comprehensive hard services programs for pharmaceutical manufacturing facility, including HVAC ...

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Pharmaceutical Engineering information

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$43

How much do pharmaceutical engineering jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for pharmaceutical engineering in Colorado is $40.44, according to ZipRecruiter salary data. Most workers in this role earn between $38.41 and $42.45 per hour, depending on experience, location, and employer.

What is pharmaceutical engineering?

Pharmaceutical engineering is a branch of engineering focused on the design, development, and manufacturing of medications and pharmaceutical products. It combines principles from chemical engineering, biomedical engineering, and pharmaceutical sciences to ensure the safe, effective, and efficient production of drugs. Professionals in this field work on process development, quality control, scaling up laboratory processes to industrial levels, and adhering to regulatory standards. Pharmaceutical engineers play a crucial role in bringing new medicines to market and maintaining the quality of existing products.

What are the key skills and qualifications needed to thrive as a pharmaceutical engineer, and why are they important?

To thrive as a Pharmaceutical Engineer, you typically need a strong background in chemical engineering, biology, or pharmaceutical sciences, supported by at least a bachelor's degree in a related field. Familiarity with industry-standard tools such as GMP (Good Manufacturing Practice) systems, process simulation software, and regulatory compliance certifications is crucial. Exceptional problem-solving abilities, attention to detail, and effective teamwork make professionals stand out in this role. These skills ensure the safe, efficient, and compliant development and manufacturing of pharmaceutical products, directly impacting patient safety and product quality.

What are some common challenges faced by pharmaceutical engineers when working on cross-functional project teams?

Pharmaceutical engineers often collaborate with professionals from research, quality assurance, regulatory, and manufacturing teams. One common challenge is aligning technical requirements with strict regulatory standards while meeting project timelines. Communication can also become complex due to the diverse expertise and priorities of each group. Successful pharmaceutical engineers proactively facilitate information sharing and adapt to feedback, ensuring that project goals are achieved without compromising quality or compliance.

What is the difference between Pharmaceutical Engineering vs Chemical Engineering?

AspectPharmaceutical EngineeringChemical Engineering
Required CredentialsBachelor's in Pharmaceutical Engineering or related field, certifications in GMPBachelor's in Chemical Engineering, professional engineering license
Work EnvironmentPharmaceutical manufacturing facilities, labsChemical plants, refineries, research labs
Industry UsagePharmaceutical companies, biotech firmsChemical, energy, and manufacturing industries

Pharmaceutical Engineering focuses on designing and optimizing processes for drug manufacturing, ensuring compliance with health regulations. Chemical Engineering has a broader scope, involving the development of chemical processes across various industries. While both roles require similar educational backgrounds, Pharmaceutical Engineers specialize in pharmaceuticals, whereas Chemical Engineers work in diverse chemical sectors.

Are pharmaceutical engineers in demand?

Pharmaceutical engineers are in demand due to the ongoing need for drug development, manufacturing, and quality assurance in the pharmaceutical industry. They often require knowledge of process engineering, regulatory standards, and specialized tools, making their skills valuable in both research and production environments.

What do pharmaceutical engineers do?

Pharmaceutical engineers design and develop processes for manufacturing drugs and medical products, ensuring they are safe, effective, and produced efficiently. They work with equipment, chemical processes, and quality control standards, often using tools like process simulation software and adhering to regulatory requirements.

What are popular job titles related to Pharmaceutical Engineering jobs in Colorado?

For Pharmaceutical Engineering jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Engineering jobs in Colorado look for?

The top searched job categories for Pharmaceutical Engineering jobs in Colorado are:

What cities in Colorado are hiring for Pharmaceutical Engineering jobs?

Cities in Colorado with the most Pharmaceutical Engineering job openings:

Pharmaceutical Engineering jobs near you
Infographic showing various Pharmaceutical Engineering job openings in Colorado as of August 2026, with employment types broken down into 8% As Needed, and 92% Full Time. Highlights an 92% In-person, and 8% Hybrid job distribution, with an average salary of $84,121 per year, or $40.4 per hour.

Senior Pharmaceutical CQV Engineer

Visium Resources, Inc.

Boulder, CO • On-site

Contractor

Re-posted yesterday

Job description

Introduction
Visium Resources has been asked to identify qualified candidates for this Pharmaceutical Senior CQV Engineer position. This position is a direct hire which is expected to be on-site in Boulder, CO.


Summary

We are seeking a highly motivated Senior CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical and biotechnology manufacturing facilities. The successful candidate will lead and execute CQV deliverables associated with GMP-regulated process equipment, utilities, automation systems, cleanrooms, and manufacturing operations.

This role requires hands-on technical expertise, strong project coordination skills, and a thorough understanding of FDA and cGMP compliance requirements. The Senior CQV Engineer will work cross-functionally with Engineering, Quality, Manufacturing, Automation, and external vendors to ensure successful project execution and operational readiness within fast-paced life sciences environments.


Key Responsibilities
  • Lead and execute CQV activities for pharmaceutical and biotech capital projects. 
  • Develop and execute: 
    • Commissioning plans 
    • IQ/OQ/PQ protocols 
    • Validation test scripts 
    • Traceability matrices 
    • Summary reports 
  • Support startup and qualification of: 
    • Process equipment 
    • Clean utilities 
    • HVAC systems 
    • Manufacturing suites 
    • Automation and control systems 
  • Coordinate field execution activities with engineering, construction, vendors, and operations teams. 
  • Perform system walkdowns and turnover package reviews. 
  • Support deviation investigations, CAPAs, and change control activities. 
  • Ensure all validation documentation complies with cGMP, FDA, ISPE, and GAMP guidelines. 
  • Participate in FAT/SAT execution and acceptance activities. 
  • Support project schedule development and milestone tracking. 
  • Collaborate with Quality Assurance and Manufacturing teams to support inspection readiness and successful system release. 
  • Mentor junior CQV engineers and validation specialists as needed.

Required Qualifications
  • Bachelor's degree in Engineering, Life Sciences, Biotechnology, or related technical discipline. 
  • 5-10+ years of CQV, validation, or pharmaceutical engineering experience within GMP-regulated environments. 
  • Strong knowledge of: 
    • cGMP regulations 
    • FDA validation requirements 
    • ISPE Baseline Guides 
    • GAMP 5 principles 
  • Experience executing commissioning and qualification for: 
    • Process equipment 
    • Utilities 
    • HVAC systems 
    • Cleanrooms 
    • Automation systems 
  • Experience authoring and reviewing validation lifecycle documentation. 
  • Strong technical writing and documentation skills. 
  • Ability to work independently within fast-paced project environments. 

Preferred Qualifications
  • Experience in biologics, sterile manufacturing, fill-finish, or aseptic processing environments. 
  • Previous consulting experience within life sciences industries preferred. 
  • Familiarity with: 
    • DeltaV 
    • MES systems 
    • SCADA platforms 
    • Kneat or electronic validation systems 
  • PMP certification or equivalent project leadership experience is a plus. 
  • Strong client-facing communication and leadership skills. 

Additional Skills & Competencies
  • Excellent organizational and multitasking abilities 
  • Strong problem-solving and analytical skills 
  • Ability to manage multiple priorities and deadlines 
  • Comfortable working in both office and field environments 
  • Ability to travel to client sites as required

________________________________________________________________________________________________


Visium Resources is an award-winning employment firm with a mission to match talented individuals with highly successful organizations. At Visium, our company's success is based on your success. When you work with us, you are never 'just a number'. You are our most important asset. Here, you will know us by name through our regular visits to client sites and even occasional luncheons. We will always be there when you need assistance and will always go the extra mile to ensure that you are as successful as possible. Whether you're looking for contract, contract-to-hire or permanent opportunities, we firmly believe there is no employment agency that will work harder for you than Visium.
Visium Resources is an equal opportunity employer and values diversity. All employment is decided based on qualifications, merit and business need.

Education:BS/BA DegreeEmployment Type: CONTRACTOR

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