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Weekday Biotech Technical Writer Jobs Near Me

C&Q Engineer, Sr.

Columbus, OH · On-site

$100K - $138K/yr

Experience with automation systems, process equipment, and utilities in pharmaceutical or biotechnology manufacturing. * Excellent technical writing, analytical, and organizational skills. * Strong ...

Pay Rate Low: 25 | Pay Rate High: 30 Our client, a renowned leader in biotechnology, is ... Strong documentation and technical writing skills. * Excellent organizational, communication, and ...

Sr Mechanical Engineer

New Albany, OH

$100K - $132K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Technical writing skills Competencies: * Established Leadership capabilities * Passion for ...

Sr Mechanical Engineer

New Albany, OH · On-site

$100K - $132K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Technical writing skills Competencies: * Established Leadership capabilities * Passion for ...

Sr Mechanical Engineer

New Albany, OH · On-site

$100K - $132K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Technical writing skills Competencies: * Established Leadership capabilities * Passion for ...

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Weekday Biotech Technical Writer information

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$66

How much do weekday biotech technical writer jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for weekday biotech technical writer in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

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The top searched job categories for Weekday Biotech Technical Writer jobs are:

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What states have the most Weekday Biotech Technical Writer jobs?

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The most popular types of Biotech Technical Writer jobs are:

A map of the United States highlighting the number of Weekday Biotech Technical Writer job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Weekday Biotech Technical Writer job openings in each state, with California having the most at 2 and Alaska the least at 0.

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

Ultimate Solutions

New Albany, OH • On-site

Full-time

Re-posted 8 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.