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Biotech Process Development Jobs in Ohio (NOW HIRING)

Amgen

Sr. Data Scientist - Process Modeling

Columbus, OH · On-site

... in biotechnology role (e.g. process engineer, scientist, data scientist) * Experience with AGILE software development methodologies * Experience with Databricks, coding languages (Python, SQL), AI ...

PSC Biotech

CQV Engineer

Columbus, OH · On-site

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Troubleshoot and resolve issues related to equipment and process performance. Collaborative with ...

IQVIA

CRA 1, IQVIA Biotech

Cleveland, OH · On-site

$71K - $145K/yr

... level financial processes or startup activities based on study needs. Accurate and timely ... We create intelligent connections to accelerate the development and commercialization of innovative ...

IQVIA

CRA 1, IQVIA Biotech

Columbus, OH · On-site

$71K - $145K/yr

... level financial processes or startup activities based on study needs. Accurate and timely ... We create intelligent connections to accelerate the development and commercialization of innovative ...

IQVIA

CRA 1, IQVIA Biotech

Cleveland, OH · On-site

$71K - $145K/yr

... level financial processes or startup activities based on study needs. Accurate and timely ... We create intelligent connections to accelerate the development and commercialization of innovative ...

IQVIA

CRA 1, IQVIA Biotech

Columbus, OH · On-site

$71K - $145K/yr

... level financial processes or startup activities based on study needs. Accurate and timely ... We create intelligent connections to accelerate the development and commercialization of innovative ...

PSC Biotech

CQV Engineer

Columbus, OH

$45 - $55/hr

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Troubleshoot and resolve issues related to equipment and process performance. * Collaborative with ...

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Biotech Process Development information

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

What are the key skills and qualifications needed to thrive in Biotech Process Development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.
What are popular job titles related to Biotech Process Development jobs in Ohio? For Biotech Process Development jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Ohio look for? The top searched job categories for Biotech Process Development jobs in Ohio are:
What cities in Ohio are hiring for Biotech Process Development jobs? Cities in Ohio with the most Biotech Process Development job openings:
Biotech Process Development jobs near you

Director of Business Development, Gene and Cell Therapy

Cincinnati Children's Office of Academic Affairs and Career Development

Cincinnati, OH

$126K - $163K/yr

Full-time

Posted yesterday

New

Job description

The Applied Gene and Cell Therapy Center (AGCTC) is a leading clinical stage center focused on advancing innovative gene and cell therapies from research through clinical translation and manufacturing. AGCTC combines expertise in translational science, process development, analytics, regulatory strategy, and GMP manufacturing to accelerate next‑generation therapies for patients with serious diseases. In addition to its research and clinical capabilities, AGCTC provides industry‑standard CDMO services, supporting process development, tech transfer, GMP manufacturing, analytical development, and quality systems for academic and industry partners. This high‑impact role is a director position focused on securing strategic partnerships with biotech and pharmaceutical companies in the Cell and Gene Therapy (CGT) space, selling complex technical solutions, scientific trust, and roadmaps to commercialization for breakthrough therapies such as CAR‑T, Gene Editing, and Viral Vectors.

Responsibilities
  • Build a new business development function from the ground up, including hiring and talent development.
  • Conduct competitive analysis of CDMO pricing, capacity trends, and emerging technologies.
  • Provide client voice feedback to the marketing team to refine value propositions and sales collateral.
  • Identify, qualify, and scout global biotech companies with CGT assets in pre‑clinical through Phase III stages.
  • Lead the entire sales cycle from initial outreach and RFPs to site visits and final execution with contract team.
  • Develop and execute regional or global business plans to meet or exceed annual booking targets.
  • Act as a bridge between client CMC needs and internal technical capabilities.
  • Represent the organization at major industry conferences.
  • Partner with key collaborators to ensure client satisfaction and identify opportunities for expansion.
Job Requirements
  • Bachelor’s degree in a related field.
  • 10+ years of experience primarily in Business Development and/or Value Proposition/Product Development Management in Gene and Cell Therapy or related life sciences; preferably 5 years in Business Development or Sales within the CDMO or Life Sciences services sector.
  • 5+ years leading cross‑functional teams in a medical device, healthcare consulting, or complex medical center environment.
  • Proven track record of closing high‑value contracts and building a pipeline from scratch.
  • Experience leading new product development and launch in a matrix organization.
  • Negotiation skills for complex legal and financial terms in MSAs and Work Orders.
  • Deep understanding of the Cell and Gene Therapy manufacturing lifecycle (viral vector production, cell processing, analytical requirements).
  • Must be able to travel up to 30% of the time, including international travel.
  • Advanced degree highly preferred.
  • Ability to present metrics such as ACV, TCV, conversion rate from Lead to Signed Proposal, and sales forecasting accuracy.
  • Established network of C‑suite and CMC‑level contacts in the cell and gene therapy ecosystem.
  • Quick rapport building in a highly technical environment.
Primary Location

Burnet Campus

Schedule

Full time

Shift

Day (United States of America)

Department

Applied Gene and Cell Therapy Center

Employee Status

Regular

FTE

1

Weekly Hours

40

Pay Range

Annualized pay may vary based on FTE status: $126,089.60 – $163,924.80

Cincinnati Children’s is proud to be an Equal Opportunity Employer committed to creating an environment of dignity and respect for all our employees, patients, and families. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, genetic information, national origin, sexual orientation, gender identity, disability or protected veteran status. EEO/Veteran/Disability

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