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Biotech Data Science Jobs in Colorado (NOW HIRING)

Danaher

Business Development Manager

Denver, CO · On-site +1

$160K - $175K/yr

... sciences, diagnostics and biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our ... data in CRM system. The essential requirements of the job include: * Minimum of a B.S. in a ...

KBI Biopharma, Inc.

Group Leader / Scientist II

Boulder, CO · On-site

$101K - $138K/yr

... data. * Responsible for analytical project team leader duties of development, clinical, and/or ... Must have knowledge of cGMPs and biotechnology-derived product regulations. Salary Range: $101,000 ...

KBI Biopharma, Inc.

Group Leader / Scientist II

Boulder, CO · On-site

$101K - $138K/yr

... data. * Responsible for analytical project team leader duties of development, clinical, and/or ... Must have knowledge of cGMPs and biotechnology-derived product regulations. Salary Range: $101,000 ...

MMS

Senior Medical Writer (Remote)

Aurora, CO · On-site

About MMS MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory ...

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Biotech Data Science information

See Colorado salary details

$39.4K

$129.1K

$206.6K

How much do biotech data science jobs pay per year?

As of Jul 15, 2026, the average yearly pay for biotech data science in Colorado is $129,062.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,600.00 and $143,000.00 per year, depending on experience, location, and employer.

Can data scientists make $300k?

Biotech data scientists can potentially earn $300,000 or more annually, especially with extensive experience, advanced skills in machine learning and bioinformatics, and working in senior or specialized roles. Compensation varies based on location, company size, and individual expertise, with some senior-level positions reaching or exceeding this salary level.

What are the most common challenges faced by professionals in Biotech Data Science roles?

One of the primary challenges in Biotech Data Science is working with large, complex, and sometimes incomplete biological datasets, which require advanced analytical approaches and careful data curation. Professionals often need to stay current with rapidly evolving technologies and methods, which can be demanding but also rewarding for those who enjoy continuous learning. Collaboration with scientists, engineers, and regulatory teams is common, so adapting communication styles and translating technical findings to diverse audiences is key. Overcoming these challenges leads to meaningful scientific discoveries and significant career growth opportunities.

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

To thrive in Biotech Data Science, you need a solid background in biology or biotechnology, strong statistical and analytical skills, and experience with data analysis languages like Python or R. Familiarity with bioinformatics tools, sequencing platforms, and data visualization software is often expected, with certifications in data science or related fields considered a plus. Excellent problem-solving, communication, and collaboration skills are essential when working across multidisciplinary teams. These competencies enable effective interpretation of complex biological data, driving innovation and insights in the biotech industry.

What is a biotech data scientist?

A biotech data scientist analyzes biological and medical data to support research and development in the biotechnology industry. They use skills in statistics, programming, and machine learning, often working with tools like Python, R, and SQL to interpret complex datasets and inform decision-making.

What is a Biotech Data Science job?

A Biotech Data Science job involves analyzing complex biological and pharmaceutical data to drive research, innovation, and decision-making. Professionals in this field use machine learning, statistical modeling, and bioinformatics tools to extract insights from genomics, clinical trials, and drug discovery datasets. They collaborate with scientists, engineers, and healthcare professionals to improve treatments, develop new therapies, and optimize bioprocesses. Strong programming skills, domain knowledge in biology or biotechnology, and expertise in data analysis are essential for success in this role.

How can data science be used in biotechnology?

Biotech data scientists analyze large biological datasets to identify patterns, develop predictive models, and optimize processes such as drug discovery, genetic research, and personalized medicine. They use tools like machine learning, statistical analysis, and bioinformatics software to support research and development efforts in biotechnology companies and labs.

Can a biotechnologist become a data scientist?

A biotechnologist can become a data scientist by acquiring skills in programming, statistics, and machine learning, often through additional training or education such as online courses or advanced degrees. Their background in biology and laboratory data can provide a strong foundation for analyzing complex datasets in data science roles within biotech and healthcare industries.
What are popular job titles related to Biotech Data Science jobs in Colorado? For Biotech Data Science jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Biotech Data Science jobs in Colorado look for? The top searched job categories for Biotech Data Science jobs in Colorado are:
Biotech Data Science jobs near you
Infographic showing various Biotech Data Science job openings in Colorado as of July 2026, with employment types broken down into 6% Internship, and 94% Full Time. Highlights an 87% In-person, and 13% Remote job distribution, with an average salary of $129,062 per year, or $62 per hour.
BIOPHARMACEUTICAL - C&Q Manager

BIOPHARMACEUTICAL - C&Q Manager

MMR Consulting

Boulder, CO • On-site

Other

Posted 5 days ago

Job description

Previous Pharmaceutical/Biotech experience is mandatory for this role.
MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation.
MMR Consulting has offices in Canada, USA, and Australia.
This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers involved in the design, commissioning & qualification, start-up and project management of various processes, systems, and facilities. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers.
This role is for C&Q Manager will require to work on the validation of upstream and downstream bioprocess systems/equipment in the biopharmaceutical industry, as well as process equipment in pharma/biotech industries. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers.
The work will require working out of client's facilities, which are in Boulder, Colorado.
Responsibilities
  • Provide technical guidance into the commissioning, qualification and start-up of various equipment and facilities used in life science manufacturing, such as bioreactors, tanks, CIP, Buffers, Media, Chrom, TFF, washers & autoclaves, etc.
  • Lead the development of key qualification deliverables during the project lifecycle to ensure project is well defined, and the action plan to test the system is applicable and relevant.
  • Lead qualification processes throughout the project lifecycle such as VPP, Risk Assessments, RTM, DQ, FAT, SAT, IQ, OQ and PQ as appropriate to ensure timely completion and to ensure all specifications are met.
  • Prepare protocols, execute protocols, summarize data, resolve deviations, prepare final reports.
  • Experience with C&Q of upstream or downstream bioprocess systems is required. Experience with C&Q of other process equipment, utilities, facilities is an asset. Thermal Validation experience is an asset.
  • Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, provide updates.
  • Engage other departments, as required, for design reviews and decisions.
  • Travel may be occasionally required for meetings with clients, equipment fabrication vendors or Factory Acceptance Testing (FATs).
  • Work may require occasional support over shutdowns or extended hours, specifically during installation and commissioning / validation phases.
  • Client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc.
  • Visit construction and installation sites following all site safety requirements.
  • Other duties as assigned by client, and/or MMR, based on workload and project requirements.

Qualifications
  • Excellent written and spoken English is required including the preparation of technical documents in English
  • Years of experience: 8+ years for years of experience in commissioning, qualification or validation of various systems within the pharmaceutical/biotech industry.
  • Knowledge of requirements for a cGMP operations, including SOPs, Change Controls, Validation.
  • Experience with developing and executing validation projects. Risk-Based Commissioning & Qualification approaches, such as ASTM E-2500 or ISPE ICQ, is considered an asset, but not required.
  • Experience with commissioning and qualification of biotech process equipment (upstream or downstream or both), such as some, but not all, of the following: fermentation, bioreactors, downstream purification processes (chromatography, TFF, UF) is required
  • Experience with commissioning & qualification of process control systems (i.e. PCS, SCADA, Historians) and building automation systems (i.e. Siemens Insight / Desigo, JCI Metasys) are considered an asset, but not required.
  • Experience with Qualification or Validation of clean utilities, ISO clean rooms, and Thermal Validation is considered an asset.
  • Experience with preparation and execution of URS's, DQ's, RTMs, Risk Assessments, CPPs, VPPs, FATs, SATs, IOQs, NCRs, Final Reports.
  • Ability to lift 50 lbs.
  • Science degree, or equivalent studies such as Mechanical, Electrical, Chemical, Biochemical, Electromechanical or a related discipline along with industry experience.
  • Ability to handle multiple projects and work in a fast-paced environment.
  • Strong multi-tasking skills

Compensation: 90,000$ - 145,000$ based on experience.
Equal Employment Opportunity and Reasonable Accommodations
MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.

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