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Associate Downstream Process Development Scientist Jobs in Ohio

Sie haben ein abgeschlossenes Studium in Biowissenschaften, Biochemie oder einer vergleichbaren Fachrichtung * Mehrjährige Erfahrung im Upstream Processing innerhalb der pharmazeutischen oder ...

Associate or Bachelor's degree in engineering or a scientific field (or equivalent experience). * 1 ... Basic data analysis skills used in process development. ***This is a complete list of all desired ...

Our skilled scientists and R&D teams are committed to enhancing product performance and providing exceptional technical support. Position Summary We are seeking an experienced Process Development ...

$90 - $130/hr

Clinical Development ScientistSkip to main content# CareersClinical Development Scientist page is ... Experienced in regulatory compliance, process improvement and project management* Experience with ...

Our skilled scientists and R&D teams are committed to enhancing product performance and providing exceptional technical support. Position Summary We are seeking an experienced Process Development ...

$90 - $120/hr

Job Title Clinical Development Scientist Job Responsibilities * Owns and drives end‑to‑end ... Experienced in regulatory compliance, process improvement and project management * Experience with ...

The R&D Scientist is responsible for the research and development of polymer compounds and ... Experience with thermoplastic polymer processing, including internal mixing, two and three roll ...

The R&D Scientist is responsible for the research and development of polymer compounds and ... Experience with thermoplastic polymer processing, including internal mixing, two and three roll ...

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Associate Downstream Process Development Scientist information

What is an associate downstream process development scientist?

An Associate Downstream Process Development Scientist is a professional who works in the biotechnology or pharmaceutical industry, focusing on developing and optimizing processes that purify biological products, such as proteins or antibodies, after they have been produced by cells. Their work is crucial for ensuring the final product meets quality and safety standards before it is used in research or clinical applications. They typically perform laboratory experiments, analyze data, and collaborate with other scientists and engineers to improve yield and efficiency. This role is often entry-level or early-career, providing hands-on experience in process development and technical troubleshooting.

What are some typical challenges faced by an associate downstream process development scientist, and how can they be addressed?

Associate Downstream Process Development Scientists often encounter challenges such as optimizing purification processes, troubleshooting equipment performance, and ensuring batch-to-batch consistency. These challenges can be addressed by maintaining meticulous documentation, collaborating closely with upstream and analytical teams, and staying current with best practices in chromatography and filtration. Proactively seeking feedback from experienced colleagues and participating in cross-functional meetings can also help in identifying solutions and improving process efficiency.

What are the key skills and qualifications needed to thrive as an associate downstream process development scientist, and why are they important?

To excel as an Associate Downstream Process Development Scientist, you need a solid understanding of biochemistry, chemical engineering, and downstream purification techniques, often supported by a bachelor's or master's degree in a life science or engineering discipline. Familiarity with chromatographic systems (such as AKTA), filtration equipment, and analytical tools, as well as knowledge of GMP/GLP regulations, is typically required. Strong problem-solving, attention to detail, and effective teamwork and communication skills help you navigate complex experiments and collaborate with cross-functional teams. These skills ensure efficient process optimization, compliance with regulatory standards, and successful development of biopharmaceutical products.

What is the difference between Associate Downstream Process Development Scientist vs Associate Upstream Process Development Scientist?

AspectAssociate Downstream Process Development ScientistAssociate Upstream Process Development Scientist
Primary FocusPurification and recovery of bioproductsCell culture and fermentation processes
Required SkillsProtein purification, chromatography, filtrationCell culture, bioreactor operation, media preparation
Work EnvironmentLaboratories, manufacturing facilitiesLaboratories, bioreactor labs
Common CertificationsBiotech or bioprocessing certificationsBiotech or bioprocessing certifications

Both roles are essential in biopharmaceutical development, focusing on different stages of the production process. The Associate Downstream Process Development Scientist specializes in purification techniques, while the Associate Upstream Process Development Scientist concentrates on cell growth and fermentation. Understanding these distinctions helps candidates target their skills and career paths effectively.

What are the most commonly searched types of Downstream Process Development Scientist jobs in Ohio?

The most popular types of Downstream Process Development Scientist jobs in Ohio are:

Associate Scientist I, Process Development Downstream

Forge Biologics

Columbus, OH

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 4 days ago


Job description

Forge Your Future with Us:

At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is simple yet powerful: to enable access to life-changing gene therapies and help bring them from ideas into reality. We partner with scientists, physicians, biotech and pharma innovators, and patient communities — all united by one goal: improving lives. If you're driven by purpose and excited to make a tangible impact, this is where your journey begins.

Our team works out of The Hearth, a state-of-the-art, 200,000-square-foot cGMP facility in Columbus, Ohio. Here, you won't just watch innovation happen — you'll be part of it. Whether you're scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting complex technical projects, you'll play a key role in bringing hope to patients with genetic diseases.

What sets Forge apart is our culture of H.O.P.E. We are hardworking, showing up each day with determination and grit. We are open, creating a space where ideas flow freely, and every voice is valued. We are purpose-driven, with every task directly tied to changing lives. And we are engaged, energized by the challenges we face and the milestones we achieve together.

At Forge, your growth matters. We're committed to helping you expand your skills, take on new challenges, and develop your career through mentorship, hands-on learning, and opportunities for advancement. Our people are our greatest investment, and we're proud to see team members grow with us.

If you're ready to use your talent to help deliver hope to patients around the world, join us — and be part of something bigger than yourself.

About The Role:   

The Associate Scientist I engages in process development activities on a full-time basis and applies basic concepts of purification under close supervision. This person is expected to work closely with cross-functional teams to support in the  development and optimization of AAV purification processes, data analysis and summary reports on a timely basis while maintaining compliance and readiness.  

Responsibilities: 

  • Learns and contributes to downstream process development activities with supervision  
  • Builds foundational skills in purification techniques such as buffer preparation, filtration, column chromatography, buffer exchange, clarification techniques, lab cleaning and routine equipment sanitization and monitoring.  
  • Expected to abide by all safety protocols and contribute to lab maintenance activities.  
  • Collaborates with peers to support experiments and begins contributing to data discussions and problem-solving in team settings.  
  • Learns to write simple study plans, PowerPoint presentations and internal reports with guidance. 
  • Documents all work clearly and contemporaneously in lab notebooks and electronic systems, ensuring same-day data entry, accuracy and traceability.  
  • Develops an understanding of downstream process development principles and begins learning how purification processes align and with cGMP requirements. 

Qualifications: 

  • Associate's, Bachelor's or certification, in Chemical Engineering, Biology, Molecular Biology, Virology, Biochemistry or related discipline or relevant coursework; 0–1 year of experience OR equivalent practical experience.  
  • Prior experience through internships, job shadowing, or on-the-job learning. 

Preferred Skills: 

  • Basic experience in laboratory skills such as buffer manufacturing, steam sterilization etc.  
  • Basic data analysis and visualization using excel and PowerPoint skills 
  • Basic experience with other aspects of downstream purification (e.g. – clarification/filtration, lab scale FPLC chromatography systems, TFF, etc.) 

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned.  

  

Work Environment and Physical Demands   

This position works in both a laboratory environment and typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area.  

Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.  

At Forge Biologics, we believe our people deserve to be taken care of – in and out of the workplace. We've built a comprehensive compensation and benefits package designed to help you thrive, grow, and feel valued every step of the way:

Health from day one

  • Health, dental and vision insurance start your first day – with 90% of premiums covered for you and your family.

Time to recharge

  • A competitive paid time off plan – because rest fuels innovation.
  • 12 weeks of fully paid parental leave so you can focus on family when it matters most.

Rewarding your impact

  • Annual bonus opportunities for all full-time team members.
  • 401(k) with company match to help you plan for the future.
  • Special employee discounts, including childcare and dependent care savings.

Your wellness, supported

  • Onsite fitness facility at The Hearth.
  • Mental health counseling and financial planning services through our Employee Assistance Program.
  • Employer-paid short and long-term disability coverage to protect your peace of mind.

Fuel for your workday

  • A fully stocked kitchen with free snacks and beverages – we keep you energized and ready for what's next.

Grow with us

  • Ongoing professional development resources, training, and mentorship programs to help you build your care and grow within Forge.