Landmark Bio

Landmark Bio

Cell and gene therapy CDMO services

Overview

Landmark Bio is a contract development and manufacturing organization (CDMO) focused on cell and gene therapy. It provides end-to-end services including drug development consulting, process analytical development, cGMP manufacturing, and CMC regulatory consulting to turn research into clinical programs. Its offerings are tailored services rather than products, delivered through collaborations with academia, physicians, biopharma, and research hospitals to address manufacturing costs and complexities. Its goal is to help programs reach clinical trials and commercial use faster while meeting regulatory standards and budget constraints, increasing patient access to advanced therapies.

About Landmark Bio

Simplify's Rating
Why Landmark Bio is rated
B-
Rated B on Competitive Edge
Rated B on Growth Potential
Rated C on Differentiation

Industries

Consulting

Industrial & Manufacturing

Biotechnology

Healthcare

Company Size

51-200

Company Stage

N/A

Total Funding

N/A

Headquarters

Watertown, Massachusetts

Founded

N/A

Simplify Jobs

Simplify's Take

What believers are saying

  • Artis BioSolutions acquisition on April 2, 2025, expands end-to-end preclinical to commercial solutions.
  • ARPA-H award integrates advanced upstream, downstream technologies to overcome batch limitations.
  • Deep expertise from 150 tech transfers, 46 BLAs, and 45 approved products attracts biopharma clients.

What critics are saying

  • Larger CDMOs like Catalent and Lonza erode market share in 12-24 months.
  • Galapagos terminates CAR-T contract after batch failures in 6-12 months.
  • Artis diverts resources from Landmark within 3-6 months post-acquisition.

What makes Landmark Bio unique

  • Landmark Bio offers modular cGMP suites for LVV, AAV, cell processing, mRNA, and novel modalities.
  • Secured up to $18.3M ARPA-H funding on April 1, 2026, for continuous EV manufacturing platform.
  • Signed manufacturing agreement with Galapagos for oncology CAR-T cell therapy.

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Benefits

Health Insurance

Unlimited Paid Time Off

Flexible Work Hours

Hybrid Work Options

Professional Development Budget

Conference Attendance Budget

Wellness Program

Mental Health Support

Stock Options

Company Equity

401(k) Retirement Plan

401(k) Company Match

Phone/Internet Stipend

Home Office Stipend

Company News

Business Wire
Feb 17th, 2026
Artis BioSolutions names Dr Kate Broderick chief scientific innovation officer to advance synthetic DNA strategy

Artis BioSolutions has appointed Dr Kate Broderick as Chief Scientific Innovation Officer, effective 9 February 2026. She will lead scientific strategy and innovation initiatives across the company's platform for developing and manufacturing genetic medicines. Dr Broderick brings over 25 years of experience in nucleic acid medicine and DNA- and RNA-based vaccine development. Most recently, she served as Chief Innovation Officer at Maravai LifeSciences. Previously, at Inovio Pharmaceuticals, she led R&D teams that advanced multiple clinical-stage programmes, including a DNA-based COVID-19 vaccine through Phase 3 testing, and secured over $100 million in non-dilutive funding. The appointment comes as Artis prepares to close its acquisition of Syngoi Technologies, expected in the first quarter of 2026. Dr Broderick holds a PhD in Molecular Genetics from the University of Glasgow.

Business Wire
Apr 3rd, 2025
Artis BioSolutions Emerges from Stealth, Announces Acquisition of Landmark Bio

Artis BioSolutions, a company founded to streamline the discovery, development and production of genetic medicines, today announced its launch, alongside its...

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