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At Cdmo Jobs (NOW HIRING)

NewAmsterdam Pharma Company N.V.

Director, CMC Analytical

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Provide technical leadership and guidance to analytical development work, methods, and testing activities at CDMO * Oversee the establishment of testing methodology, specifications, and stability ...

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$15K

$241.3K

$387K

How much do at cdmo jobs pay per year?

As of Aug 14, 2026, the average yearly pay for at cdmo in the United States is $241,295.00, according to ZipRecruiter salary data. Most workers in this role earn between $200,000.00 and $300,000.00 per year, depending on experience, location, and employer.

What is the difference between At Cdmo vs Clinical Research Associate?

AspectAt CdmoClinical Research Associate
Required credentialsTypically requires a degree in life sciences, pharmacy, or related field; certifications varyRequires a degree in life sciences or healthcare; often requires GCP or ICH certifications
Work environmentContract manufacturing or development labs, regulatory compliance settingsClinical trial sites, hospitals, or research organizations
Employer and industry usagePharmaceutical, biotech, and contract manufacturing organizationsPharmaceutical companies, CROs, research institutions

While both roles involve the pharmaceutical industry, At Cdmo professionals focus on manufacturing and development processes within CDMOs, whereas Clinical Research Associates oversee clinical trial activities at research sites. The credentials and work environments overlap but serve different stages of drug development.

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At Cdmo jobs near you
Infographic showing various At Cdmo job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 82% In-person, and 18% Remote job distribution, with an average salary of $241,295 per year, or $116 per hour.

Senior Research Associate, Cell Culture

Vistera Inc

Waltham, MA • On-site

$95K - $126K/yr

Full-time

Posted 10 days ago

Job description

The Senior Research Associate is a key member of the growing Pharmaceutical Sciences and Technology team and is responsible for executing cell culture development activities in our laboratory and contributing to projects with our partner organizations.
Reporting to the Senior Process Scientist (the leader of the cell culture team), the Senior Research Associate role will execute cell line development workflows and cell culture development experiments in our laboratory. The Senior Research Associate will also contribute to contracted activities at Contract Development and Manufacturing Organizations (CDMOs). The individual will work closely with internal partners in Quality Assurance, Research, and Regulatory as well as with external partners.
Responsibilities
  • Conducting shake flask and bioreactor operations for small scale development and characterization of cell culture processes for Visterra's antibody products.
  • Conducting cell line development activities in line with regulatory guidance to establish Research Cell Banks for use in GMP Master Cell Bank generation.
  • Assist with developing producer cell lines from DNA construct assembly through genetic stability testing.
  • Independently prepare DNA vectors using standard molecular biology techniques including homology-based cloning, transformation and propagation in bacteria, and kit-based purification.
  • Independently execute work to develop cell culture platform processes to support in-house material generation to support research and pre-clinical studies.
  • Independently operating laboratory cell culture equipment including bench-scale bioreactors, shake flasks, and multiwell plates.
  • Monitoring and sampling of cell culture processes daily; including testing for attributes such as cell viability and density, metabolites, pH, and more.
  • Contribute to cell culture technology transfer activities including:
  • reviewing and presenting process data
  • troubleshooting results of small scale and pilot scale data
  • performing scaleup calculations
  • Support GMP manufacturing through review of Batch Records and support for deviation investigations
  • Support GMP manufacturing as a Person-in-Plant representing Visterra at CDMO sites.
  • Presenting work at department and cross functional meetings and presenting relevant updates on lab activities at drug development team meetings.
  • Troubleshooting and maintaining laboratory equipment.
  • Documenting experimental results in lab notebooks, tech transfer documents, and technical reports and presenting data at meetings.
  • Keeping current with new technologies to improve process development capabilities.
  • Traveling up to 10% of the time for site visits at CDMOs and to attend conferences

Requirements
  • B.S. in Pharmaceutical Sciences, Biochemistry, Biology, Chemical Engineering, or Biological Engineering (or related disciplines) with 3 years of relevant industry experience, or M.S. with 1 years of relevant industry experience
  • Experience in maintaining and troubleshooting mammalian cell culture operations.
  • A strong understanding of cell culture parameters in general (cell growth rate, cell density, viability, population doubling, metabolites and cell waste, etc.).
  • Hands-on experience with aseptic techniques for mammalian cell culture operations.
  • Experience with transfection of mammalian cells for transient and/or stable expression of genes of interest.
  • The ability to think critically and communicate effectively across broad spectrum of audiences both internal and external.
  • An ability to work independently, meet deadlines and prioritize work effectively.
  • The ability to travel to conferences and global manufacturing sites up to 10% of the time.
  • Due to the nature of cell culture activities, some work outside of non-standard hours, including weekend work is required.

Company
Visterra is a clinical stage biotechnology company committed to developing innovative antibody-based therapies for the treatment of patients with kidney, immune-mediated and other hard-to-treat diseases. Our proprietary technology platform enables the design and engineering of precision antibody-based product candidates that specifically bind to, and modulate, key disease targets. Applying this technology to disease targets that are not adequately addressed by traditional therapeutic approaches, we are developing a robust pipeline of novel therapies for patients with unmet needs. Visterra's pipeline has multiple clinical-stage assets and one approved therapeutic, sibeprenlimab.
As a member of the Otsuka family of companies, we are uniquely positioned as a small, dynamic, nimble and innovative organization where individuals and teams are empowered to make big impacts - while benefiting from the support, strength, stability and long-term perspective of a 100-year-old global company. Visterra has approximately 105 employees and is located in Waltham, Massachusetts.
Visterra 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.

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