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Biotech Operations Manager Jobs in Colorado (NOW HIRING)

Research Project Manager

Boulder, CO ยท On-site

$95K - $110K/yr

Works independently, can manage interactions with and between internal teams and external partners, and brings strong program operations capability in a fast-paced biotech environment.

As an operations consulting generalist at PwC, you will possess a broad understanding of various ... Mathematics, Biotechnology preferred - Prior consulting or advisory firm experience preferred ...

Jun 11, 2026 Our WW Operations network delivers millions of packages and smiles to Amazon customers ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

Jun 14, 2026 Our WW Operations network delivers millions of packages and smiles to Amazon customers ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

Jun 12, 2026 Our WW Operations network delivers millions of packages and smiles to Amazon customers ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

Jun 11, 2026 Our WW Operations network delivers millions of packages and smiles to Amazon customers ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

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Biotech Operations Manager information

See Colorado salary details

$32.6K

$66.7K

$124.6K

How much do biotech operations manager jobs pay per year?

As of Jun 12, 2026, the average yearly pay for biotech operations manager in Colorado is $66,725.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,100.00 and $81,500.00 per year, depending on experience, location, and employer.

What are some common challenges faced by Biotech Operations Managers, and how can they be addressed?

Biotech Operations Managers often face challenges such as maintaining regulatory compliance, managing cross-functional teams, and ensuring smooth production processes. These challenges can be addressed by staying updated on industry regulations, fostering clear communication between departments, and implementing robust quality control systems. Additionally, leveraging project management tools and continuous process improvement strategies can help streamline operations and minimize risks.

What is the difference between Biotech Operations Manager vs Biotech Laboratory Supervisor?

AspectBiotech Operations ManagerBiotech Laboratory Supervisor
CredentialsBachelor's or Master's in Life Sciences, Business, or related fields; experience in biotech operationsBachelor's or Master's in Life Sciences; laboratory management experience; relevant certifications often preferred
Work EnvironmentOversees multiple departments, manages projects, and ensures compliance across operationsManages daily lab activities, supervises lab staff, and maintains lab safety and procedures
Employer & Industry UsageUsed in biotech companies for operational oversightCommon in research labs, biotech firms, and pharmaceutical companies for lab management

The Biotech Operations Manager focuses on overseeing overall biotech operations, including project management and compliance, while the Biotech Laboratory Supervisor concentrates on managing daily lab activities and staff. Both roles require relevant scientific credentials, but their scope and responsibilities differ significantly.

What are the key skills and qualifications needed to thrive as a Biotech Operations Manager, and why are they important?

To thrive as a Biotech Operations Manager, you need a solid background in life sciences, business management, and regulatory compliance, often supported by a relevant degree and industry experience. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and project management tools is typically required, along with certifications like Six Sigma or PMP being advantageous. Strong leadership, problem-solving abilities, and effective communication are crucial soft skills for managing teams and cross-functional projects. These skills ensure efficient operations, regulatory adherence, and successful product delivery in the highly regulated biotech industry.

What does a Biotech Operations Manager do?

A Biotech Operations Manager is responsible for overseeing the daily operations of biotechnology facilities, ensuring that production processes run efficiently and comply with industry regulations. They manage teams, coordinate schedules, oversee supply chains, and implement quality control measures. Additionally, they work closely with research and development, regulatory, and quality assurance teams to ensure products meet all safety and efficacy standards. Their role is crucial in maintaining productivity, safety, and compliance in a biotech organization.
What are popular job titles related to Biotech Operations Manager jobs in Colorado? For Biotech Operations Manager jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Biotech Operations Manager jobs in Colorado look for? The top searched job categories for Biotech Operations Manager jobs in Colorado are:
What cities in Colorado are hiring for Biotech Operations Manager jobs? Cities in Colorado with the most Biotech Operations Manager job openings:
Infographic showing various Biotech Operations Manager job openings in Colorado as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $66,725 per year, or $32.1 per hour.
Senior Manager, Quality Assurance Operations

Senior Manager, Quality Assurance Operations

Umoja Biopharma

Louisville, CO โ€ข On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 15 days ago


Job description

Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.
Umoja Biopharma - Your Body. Your Hope. Your Cure.
POSITION SUMMARY
Umoja Biopharma is seeking a Senior Manager, Quality Assurance (QA) Operations to support GMP operations at Umoja's state-of-the-art lentiviral vector development and manufacturing facility, The CLIMB, in Louisville, CO. This position delivers leadership and management oversight of the QA Operations team, which provides QA partnership and oversight of all GxP functions (e.g., Manufacturing, Supply Chain, Facilities, Engineering, etc.) at The CLIMB.
This role is fully onsite at our Louisville, CO location 5 days/week. This role may require weekend, evening, or holiday work when necessary.
CORE ACCOUNTABILITIES
Specific responsibilities include:
  • Exemplifying, role modeling, and maturing Umoja's quality culture
  • Managing, building, and maturing a high-performing, solution-oriented function that nurtures strong cross-functional working relationships
  • Leading, managing, and supporting QA Operations to provide QA partnership and oversight (e.g., controlled documents, change controls, deviations, CAPAs, work orders, etc.) of GxP functions (e.g., Manufacturing, Supply Chain, Facilities, Engineering, etc.) at The CLIMB
  • Supports QA Operations teams collaborative interactions with cross-functional partners in translating applicable laws, regulations, and guidance (e.g., FDA, ICH, EMA, etc.) into compliant & efficient internal procedures and ways of working in accordance with phase-appropriate cGMPs and effective quality risk management principles
  • Engaging with key stakeholders and utilizing Operational Excellence principles and tools to drive continual improvement of the Umoja Quality Management System
  • Championing Umoja QA's "purposeful presence" initiative, ensuring productive and intentional QA partnership with cross-functional teams
  • Overseeing disposition of product and incoming materials
  • Advancing Umoja's Quality Risk Management (QRM) program and associated processes
  • Partnering with senior Quality management to develop a QA Operations functional strategy to achieve short-term and long-term organizational and company goals & objectives
  • Translating functional area strategy into an efficient tactical execution plan that prioritizes functional workload
  • Establishing, monitoring, and maturing key business performance metrics to facilitate continual improvement opportunity identification and execution.
  • Developing and maintaining capacity and resource modeling tools for the QA Operations functions
  • Development of QA Operations team through engaging, purposeful development planning and routine follow-up
  • Representing QA Operations on cross-functional leadership and project teams
  • Supporting the preparation of documents and sections for regulatory dossiers (e.g., briefing books, IND sections, BLA sections, etc.)
  • Providing support for audits and inspections, where needed
  • Providing additional Quality Assurance support and leadership, as needed

The successful candidate will have:
  • Bachelor's degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or other life science with minimum of 10+ years of work experience in an FDA regulated industry.
  • Minimum of 4+ years of successful people management experience with demonstrated ability to build, develop, and lead a high-performing team.
  • Advanced knowledge and understanding of regulatory governing bodies, requirements, and guidance documents, and how to practically apply these in a cGMP biopharmaceutical environment across different phases of product development
  • Strong understanding of foundational Quality systems (e.g., audits/inspections, documentation, NC/CAPA, Quality Risk Management, etc.)
  • Previous experience releasing product for clinical and/or commercial use
  • Independent and risk-based decision-making capability with clear understanding of decision-making impact in dynamic GMP environment
  • Ability to think and lead conceptually, strategically, and tactically, arriving at practical and pragmatic conclusions
  • Ability to translate complex processes and competing priorities into a clear, actionable plan for execution
  • Experience in cGMP cell and gene therapy manufacturing facility

Preferred Qualifications:
  • Previous experience with audits and health authority inspections
  • Previous experience providing QA oversight of sterile injectable product(s)

Physical Requirements:
  • Ability to gown aseptically and work in a Clean Room environment
  • Ability to work while gowned for extended periods of time
  • Ability to stand for extended periods of time to fulfill on-the-floor Quality duties
  • Use of laboratory equipment includes handling chemicals and biological materials
  • Must have the ability to work around laboratories, manufacturing areas and equipment, and regularly lift 10-20 lbs. and periodically lift up to 50 lbs.
  • Ability to work occasional evenings, holidays, and weekends as needed

Salary Range: $155,000 - $191,500
Benefits Offerings
Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the Benefits section of our website.