Biotech Lab Associate I: Upstream, Downstream & Formulation

Replimune

Framingham (MA)

On-site

USD 72,000 - 93,000

Full time

11 days ago

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Benefits offered by this job

Medical, dental, and vision insurance
401k match
Flexible time off
Paid holidays

Job summary

Replimune is seeking an Associate I, PDT to support day-to-day PDT laboratory operations, including upstream tissue culture, virus purification, and drug product formulation. The role is based in Framingham, MA with a typical 5‑day on-site expectation.

You will perform routine lab steps under supervision, maintain equipment and reagents, and ensure meticulous documentation in compliance with GMP and SOPs, contributing to a pivotal biotech portfolio.

Qualifications

  • Bachelor’s degree with 0–2 years of related work experience.
  • Experience in a laboratory setting preferred. Familiarity with biotech/pharma operations is advantageous.

Responsibilities

  • Support upstream tissue culture, downstream virus purification and drug product formulation activities in the PDT laboratory.
  • Perform routine laboratory and pilot process steps with supervision, including setup, sampling, and documentation.
  • Maintain stock levels of consumables and prepare reagents while following good documentation practices.
  • Ensure laboratory cleanliness, waste disposal, sample storage, and equipment monitoring.
  • Operate in accordance with GMP and company procedures as required.
  • Collaborate with Manufacturing, Quality Control, Facilities, Engineering, Analytical Development, and QA teams.
  • Document results accurately in laboratory notebooks.

Skills

Cell culture
Purification
Chromatography
Formulation
Documentation
Teamwork

Education

Bachelor’s degree in life sciences

Tools

GMP procedures

Job description

Replimune is seeking an Associate I, PDT to support day-to-day PDT laboratory operations, including upstream tissue culture, virus purification, and drug product formulation. The role is based in Framingham, MA with a typical 5‑day on-site expectation.

You will perform routine lab steps under supervision, maintain equipment and reagents, and ensure meticulous documentation in compliance with GMP and SOPs, contributing to a pivotal biotech portfolio.

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