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Biotech Startup Jobs in Colorado (NOW HIRING)

Visium Resources, Inc.

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Project Manager - Senior CQV Pharmaceutical

Boulder, CO · On-site

Support startup, operational readiness, and technology transfer activities. * Present project ... Minimum 8-12 years of experience in pharmaceutical, biotech, or life sciences industries. * Minimum ...

Visium Resources, Inc.

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Senior Pharmaceutical CQV Engineer

Boulder, CO · On-site

... and biotech capital projects. * Develop and execute: * * Commissioning plans * IQ/OQ/PQ protocols * Validation test scripts * Traceability matrices * Summary reports * Support startup and ...

Amino Collective

Accounts Payable Associate

Boulder, CO · On-site

$21 - $27/hr

... biotech, pharma, or startup environment preferred Continuous improvement mindset with a commitment to accuracy, accountability, and audit readiness If you're passionate about innovation and impact ...

Pivot Bio

Territory Sales Manager

Greeley, CO · On-site +1

$77K - $96K/yr

... biotech or agribusiness sales. * Proven success in agricultural sales and team management. Work ... Competitive package in a disruptive startup * Stock options * Health/Dental/Vision insurance with ...

Foresight Diagnostics

Program Manager

Boulder, CO · On-site +1

Following our acquisition by Natera, we now combine the agility of a mission-driven startup with ... in biotechnology, diagnostics, clinical laboratory, or life sciences * Experience supporting ...

CRB

Senior Mechanical Engineer

Denver, CO · On-site

$107.60K - $142K/yr

... startup. The Mechanical Engineer IV will serve as a technical leader and mentor, overseeing the ... Experience in life sciences (pharmaceutical, biotech, laboratory) or food & beverage industries.

CRB

Senior Mechanical Engineer

Denver, CO · Remote

$107.60K - $142K/yr

... startup. The Mechanical Engineer IV will serve as a technical leader and mentor, overseeing the ... Experience in life sciences (pharmaceutical, biotech, laboratory) or food & beverage industries.

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Biotech Startup information

See Colorado salary details

$22.1K

$89.5K

$208.5K

How much do biotech startup jobs pay per year?

As of May 29, 2026, the average yearly pay for biotech startup in Colorado is $89,482.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,066.00 and $109,195.00 per year, depending on experience, location, and employer.

What is a Biotech Startup job?

A Biotech Startup job involves working in an early-stage company that develops innovative biological or medical technologies. Roles can vary widely, including research, product development, regulatory affairs, and business operations. Employees often wear multiple hats, contributing to both scientific advancements and business growth. The fast-paced environment requires adaptability, problem-solving skills, and a passion for innovation.

What are the key skills and qualifications needed to thrive in the Biotech Startup position, and why are they important?

To thrive at a biotech startup, you need a strong background in life sciences or bioengineering, paired with an entrepreneurial mindset and practical research experience. Familiarity with laboratory equipment, data analysis software, and, in many cases, regulatory compliance certifications like GLP or GMP are vital. Exceptional adaptability, problem-solving abilities, and teamwork skills are also crucial in this fast-paced, multidisciplinary environment. These competencies help ensure innovation, rapid iteration, and successful navigation of the complex challenges faced by emerging biotech companies.

What are some unique challenges of working at a biotech startup compared to larger organizations?

Working at a biotech startup often means taking on a wide variety of responsibilities, as teams are usually small and roles can be less narrowly defined than at established companies. You may regularly transition between lab research, project management, and business development tasks, which can be both challenging and rewarding. Limited resources, tight deadlines, and the pressure to rapidly produce results are common, but these challenges also provide opportunities for accelerated learning and career advancement. Many employees find the collaborative, innovative atmosphere and the ability to make a tangible impact particularly fulfilling in this setting.
More about Biotech Startup jobs
What are popular job titles related to Biotech Startup jobs in Colorado? For Biotech Startup jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Biotech Startup jobs in Colorado look for? The top searched job categories for Biotech Startup jobs in Colorado are:
What cities in Colorado are hiring for Biotech Startup jobs? Cities in Colorado with the most Biotech Startup job openings:
Biotech Startup jobs near you
Infographic showing various Biotech Startup job openings in Colorado as of May 2026, with employment types broken down into 93% Full Time, 4% Part Time, and 3% Contract. Highlights an 59% Physical, 2% Hybrid, and 39% Remote job distribution, with an average salary of $89,482 per year, or $43 per hour.
Project Manager - Senior CQV Pharmaceutical

Project Manager - Senior CQV Pharmaceutical

Visium Resources, Inc.

Boulder, CO

Full-time

Posted 10 days ago

Job description

Introduction
Visium Resources has been asked to identify qualified candidates for a full time position as a Senior CQV Project Manager. Required to work onsite in Boulder, CO and employer will pay monthly expenses for commute. We are seeking an experienced Senior CQV Project Manager to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives. This individual will oversee cross-functional CQV execution for GMP-regulated facilities, utilities, equipment, automation systems, and manufacturing processes while ensuring compliance with FDA, cGMP, and global regulatory standards.


The ideal candidate will possess strong pharmaceutical project leadership experience within biotech, sterile manufacturing, fill-finish, API, or biologics environments and will serve as a key liaison between engineering, quality, validation, manufacturing, and external vendors. This role requires the ability to manage project schedules, budgets, risks, resources, and validation deliverables in support of facility expansions, new product introductions, and operational readiness initiatives.


Key Success Criteria
  • Experience leading major expansion C&Q projects start to finish (brownfield or greenfield). From strategy / planning through to full doc prep & execution
  • Writes CQV Strategies & Plans.
  • CQV Schedule
  • Should have experience with C&Q of process equipment.
  • Has experienced with integrated CQV (ASTM E2500 and ISPE C&Q baseline guide)
  • Has experience with digital validation (i.e. Kneat or other software) is a major asset but not required.
  • Capital Improvements experience is a major asset but not required.

Key Responsibilities
  • Lead all CQV project activities for pharmaceutical and biotech manufacturing projects.
  • Develop and manage CQV strategies, project plans, schedules, budgets, and resource allocation.
  • Coordinate commissioning and qualification activities for:
    • Process equipment
    • Clean utilities
    • HVAC systems
    • Automation and control systems
    • Manufacturing and packaging lines
  • Ensure compliance with FDA, cGMP, ISPE, GAMP, and corporate quality standards.
  • Oversee execution of:
    • FAT/SAT protocols
    • IQ/OQ/PQ protocols
    • Validation documentation
    • Deviations and CAPAs
    • Change controls
  • Collaborate with Quality Assurance, Engineering, Manufacturing, Automation, and Regulatory teams to support project milestones and inspection readiness.
  • Manage third-party CQV consultants, contractors, and vendors.
  • Provide risk assessments and mitigation strategies to maintain project timelines and compliance objectives.
  • Support startup, operational readiness, and technology transfer activities.
  • Present project status updates and KPI reporting to senior leadership and stakeholders.

Qualified candidates would have the following:

  • Minimum 8-12 years of experience in pharmaceutical, biotech, or life sciences industries.
  • Minimum 5 years of direct CQV project management experience within GMP-regulated manufacturing environments.
  • Proven experience managing large-scale capital projects, facility expansions, or greenfield startup projects.
  • Strong experience with commissioning and qualification of:
    • Cleanrooms
    • Process equipment
    • Utilities
    • Automation systems
    • Manufacturing processes
  • Experience authoring and reviewing validation lifecycle documentation.
  • Demonstrated success leading cross-functional teams and managing multiple project workstreams simultaneously.
  • Experience supporting FDA audits and regulatory inspections.
  • Background in biologics, sterile fill-finish, vaccine, API, or aseptic manufacturing environments strongly preferred.

Required Qualifications
  • Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or related technical discipline.
  • Strong understanding of:
    • cGMP regulations
    • FDA validation requirements
    • ISPE Baseline Guides (inc. C&Q) and ASTM E2500 GUIDE
    • GAMP 5 principles
  • Proficiency with project management methodologies, scheduling tools, and reporting systems.
  • Excellent communication, leadership, and stakeholder management skills.
  • Ability to work effectively in fast-paced, highly regulated project environments.

Preferred Qualifications
  • Digital Validation software experience (i.e. Kneat or equivalent)
  • PMP certification preferred.
  • Experience with DeltaV, MES, SCADA, or other pharmaceutical automation platforms.
  • Familiarity with Kneat, TrackWise, Veeva, or electronic validation systems.
  • Previous consulting or EPCM experience is a plus.

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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.