Forge Biologics

Scientist II - Manager, PD Upstream

Forge Biologics$90K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Chemical Engineering, Bioengineering, Biology, or related discipline
  • Working knowledge of mammalian cell culture techniques
  • Proven ability to operate and troubleshoot bioreactors
  • Experience in planning, conducting, and reviewing experimental data
  • Experience in training and developing team members
  • Experience in data analysis and decision-making
  • Project management experience

Responsibilities

  • Serve as a senior-level technical contributor and subject matter expert
  • Manage multiple projects or client programs simultaneously
  • Lead process development activities for various program stages
  • Design and execute complex DoE studies and author reports
  • Proactively identify and solve upstream scale-up challenges
  • Liaise between Process Development, Manufacturing, and Quality teams
  • Mentor junior scientists and associates in technical skills

Benefits

  • Comprehensive health, dental and vision insurance with 90% premium coverage
  • Competitive paid time off and 12 weeks of fully paid parental leave
  • Annual bonus opportunities and 401(k) with company match
  • Onsite fitness facility and mental health counseling services
  • Employer-paid short and long-term disability coverage
  • Free snacks and beverages in kitchen
  • Ongoing professional development resources and mentorship programs
Full Job Description
About The Role:

The Scientist II provides active leadership and execution of the laboratory experiments and protocols for upstream process development efforts. This individual will lead projects and complex experiments, train junior scientists, and actively contribute to the advancement of AAV manufacturing processes.

Responsibilities:
  • Senior-level technical contributor and subject matter expert for upstream systems and process strategy
  • Independently manages multiple projects or client programs simultaneously, maintaining a high degree of quality, scientific rigor, and compliance
  • Leads process development activities for early- to late-stage programs, including scale-up, technology transfer, and validation support
  • Designs and executes complex DoE studies, authors technical reports, and contributes to regulatory documentation
  • Anticipates challenges in upstream scale-up and proactively develops solutions to ensure technical success
  • Acts as a key liaison between Process Development, Manufacturing, and Quality teams to align on strategy and ensure smooth GMP execution
  • Contributes scientific rationale for tech transfer packages and GMP documentation without owning official SOPs or batch records
  • Mentors junior scientists and associates through day-to-day technical guidance, fostering development in experimental design, documentation standards, and scientific reasoning


Qualifications:
  • Bachelor's Degree in Chemical Engineering, Bioengineering, Biology, or related discipline (or equivalent experience)
  • Working knowledge of cell culture techniques utilizing mammalian cells
  • Proven ability to operate and troubleshoot bioreactors
  • Experience planning, conducting and reviewing experimental data with minimal oversight
  • Experience training and development of other team members
  • Experience analyzing data sets and utilizing the corresponding data to influence decision making
  • Experience working with external collaborators (clients, external technology transfers, etc.)
  • Project management experience


Preferred Skills:
  • Master's Degree or PhD in Chemical Engineering, Bioengineering, Biology, or related discipline (or equivalent experience)
  • Experience working with viral vectors (AAV, Lentivirus, 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.

We've Got You Covered:

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.

About Forge Biologics

Forge Biologics is a gene therapy contract development and manufacturing organization (CDMO) that focuses on the development and manufacturing of gene therapies for rare diseases. The company provides a full suite of services from preclinical development to commercial manufacturing. Forge Biologics is headquartered in North Canton, Ohio and was founded in 2019.
Learn more about Forge Biologics
Size
50 employees
Industry
Founded
2019

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