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Junior Developer Startup Jobs Near Me

Project I&C Engineer

Columbus, OH · On-site

$80K - $103K/yr

Mentor junior engineers and designers. Required Qualifications: * Bachelor's degree in Mechanical ... PLC/HMI programming, configuration & startup experience Why Arcadis? We can only achieve our goals ...

Project I&C Engineer

Columbus, OH · On-site

$80K - $104K/yr

Mentor junior engineers and designers. Required Qualifications: * Bachelor's degree in Mechanical ... PLC/HMI programming, configuration & startup experience Why Arcadis? We can only achieve our goals ...

Immuta has been recognized by Forbes as a top American startup employer, by Inc. Magazine and ... Provide technical leadership, mentoring junior engineers and fostering a culture of learning and ...

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How much do junior developer startup jobs pay per year?

As of Aug 10, 2026, the average yearly pay for junior developer startup in the United States is $88,976.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,000.00 and $87,000.00 per year, depending on experience, location, and employer.
What cities are hiring for Junior Developer Startup jobs? Cities with the most Junior Developer Startup job openings:
What states have the most Junior Developer Startup jobs? States with the most job openings for Junior Developer Startup jobs include:
What are the most commonly searched types of Developer Startup jobs? The most popular types of Developer Startup jobs are:
A map of the United States highlighting the number of Junior Developer Startup job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Junior Developer Startup job openings in each state, with California having the most at 2 and Hawaii the least at 0.

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

Ultimate Solutions

New Albany, OH • On-site

Full-time

Re-posted 4 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.