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Biotechnology Startup Jobs (NOW HIRING)

Research Assistant - Protein Production Scientist at Argonne National Laboratory, Lemont, IL Our client, Argonne National Laboratory is hosting a new early-stage biotech startup developing ...

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Biotechnology Startup information

What are the key skills and qualifications needed to thrive in a biotechnology startup, and why are they important?

To thrive in a biotechnology startup, you need a strong background in life sciences, research methodologies, and often an advanced degree such as a Ph.D. or M.S. in a relevant field. Experience with laboratory techniques, data analysis software, and familiarity with regulatory compliance tools like GLP or GMP are typically required. Entrepreneurial mindset, adaptability, and strong communication skills set individuals apart in the fast-paced startup environment. These skills are crucial for driving innovation, ensuring scientific rigor, and successfully navigating the unique challenges of early-stage biotech companies.

What are some common challenges faced by employees working at a biotechnology startup?

Employees at biotechnology startups often encounter challenges such as rapidly changing priorities, limited resources, and tight deadlines. The work environment is typically fast-paced and requires adaptability, as team members may need to wear multiple hats and take on tasks beyond their primary job description. Collaboration across interdisciplinary teams—such as research, product development, and business operations—is crucial for success. Despite these challenges, the dynamic atmosphere offers significant opportunities for professional growth and learning.

What is a biotechnology startup?

A biotechnology startup is a newly established company that leverages biological systems, organisms, or derivatives to develop innovative products or services, often in sectors like healthcare, agriculture, or environmental science. These startups typically focus on research and development to solve real-world problems using cutting-edge biological and technological approaches. They may work on developing new drugs, diagnostic tools, genetically modified crops, or sustainable materials. Biotechnology startups often require significant scientific expertise, access to laboratory equipment, and funding to bring their innovations to market.

What is the difference between Biotechnology Startup vs Biotechnology Research Scientist?

AspectBiotechnology StartupBiotechnology Research Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Biology, or related fields; entrepreneurial skillsMaster's or Ph.D. in Biotechnology, Biology, or related fields; research expertise
Work EnvironmentFast-paced, dynamic, startup setting; cross-functional teamsLaboratory, academic or corporate research settings; focused on experiments
Employer & Industry UsageStartups, biotech firms, innovation-driven companiesResearch institutions, universities, biotech companies

Biotechnology startups focus on developing new products and solutions in a fast-paced environment, often requiring entrepreneurial skills. In contrast, biotechnology research scientists primarily conduct experiments and studies to advance scientific knowledge. Both roles require strong biotech credentials, but their work settings and objectives differ significantly.

More about Biotechnology Startup jobs
What cities are hiring for Biotechnology Startup jobs? Cities with the most Biotechnology Startup job openings:
What states have the most Biotechnology Startup jobs? States with the most job openings for Biotechnology Startup jobs include:
Infographic showing various Biotechnology Startup job openings in the United States as of June 2026, with employment types broken down into 96% Full Time, 3% Part Time, and 1% Contract. Highlights an 73% Physical, 2% Hybrid, and 25% Remote job distribution.
Commissioning & Qualification Engineer, Jr. - New Albany, Ohio

Commissioning & Qualification Engineer, Jr. - New Albany, Ohio

Ultimate Solutions

New Albany, OH • On-site

Full-time

Posted 28 days ago


Job description

Commissioning & Qualification Engineer, Jr.
At Ultimate Solutions, we deliver engineering, automation, serialization, and compliance solutions to the world's leading pharmaceutical, biotechnology, medical device, and logistics companies.
For more than 20 years, our team has successfully supported complex manufacturing and packaging projects across Puerto Rico, the United States, and Europe. We are known for delivering high-impact technical solutions, strong client partnerships, and exceptional project execution in highly regulated industries.
We are currently seeking a motivated and hands-on Commissioning & Qualification (C&Q) Engineer, Jr. to support exciting biotech manufacturing startup and expansion projects in New Albany.
This is an excellent opportunity for engineers with solid GMP experience who want to grow their careers while working alongside experienced industry leaders in a fast-paced and highly technical environment.
What You'll Do
  • Support commissioning and qualification activities for process equipment, utilities, facilities, packaging systems, and automation platforms.
  • Execute and document IQ, OQ, and PQ protocols in compliance with GMP and regulatory requirements.
  • Assist with startup, troubleshooting, testing, and system turnover activities.
  • Develop and review C&Q documentation including protocols, reports, test scripts, and traceability matrices.
  • Verify systems meet design specifications, user requirements, and operational expectations.
  • Collaborate with engineering, automation, validation, manufacturing, and quality teams to meet project milestones.
  • Support deviation investigations, change controls, and CAPA activities.
  • Maintain accurate, audit-ready documentation throughout project execution.
  • Travel to OEM/vendor facilities to support and execute Factory Acceptance Testing (FAT) and validation activities prior to equipment shipment and site installation.
  • Promote safe work practices and compliance with environmental and quality standards.

What We're Looking For
  • Bachelor's degree in Engineering, Life Sciences, or a related technical field.
  • Minimum of 2 years of solid experience in Commissioning, Qualification, Validation, or related GMP-regulated activities.
  • Experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
  • Working knowledge of IQ/OQ/PQ methodologies, GMP regulations, and industry standards.
  • Ability to read and interpret P&IDs, engineering drawings, and technical documentation.
  • Strong technical writing, organizational, and problem-solving skills.
  • Team-oriented mindset with excellent communication skills.
  • Ability and willingness to travel to OEM/vendor facilities for FAT execution and project support.
  • Willingness to work in a dynamic, schedule-driven project environment.

Preferred Qualifications
  • Experience supporting biotech or pharmaceutical startup projects.
  • Familiarity with ISPE Baseline Guides and ASTM E2500.
  • Exposure to automation systems, utilities, or process equipment qualification.
  • Knowledge of risk-based C&Q methodologies.
  • Experience supporting deviations, investigations, and change control processes.

Why Join Ultimate Solutions?
  • Work on cutting-edge biotech manufacturing projects.
  • Join a collaborative and highly technical engineering team.
  • Career growth opportunities within a global engineering organization.
  • Exposure to large-scale GMP startup and expansion projects.
  • Competitive compensation and professional development opportunities.

Not open for Corp-to-Corp arrangements
Equal Opportunity Employer

Ultimate Solutions is an Equal Opportunity Employer. We are committed to creating an inclusive workplace where all employees and applicants are treated with respect and provided equal employment opportunities regardless of race, color, religion, sex, national origin, disability, veteran status, or any other protected characteristic under applicable law.