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Salary
≈ $46k – $95k per year (Estimated)
Location
In office (Portland)
Seniority
Junior · 2+ years exp
Visa
H-1B filings in 12 months: 15 · green card filings: 5
Employment
Contractor

Confirmed on the employer's own hiring board on Oct 18, 2026. First seen by Alion on Jul 28, 2026. Twist Bioscience scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Twist Bioscience is a synthetic biology company headquartered in South San Francisco, California that manufactures synthetic DNA on a silicon-based platform. Founded in 2013 and listed on Nasdaq, it sells genes, oligo pools, NGS target enrichment panels and library preparation kits, variant libraries and antibody discovery services to researchers in pharma, biotech, diagnostics and academia, with production in South San Francisco and Wilsonville, Oregon and teams in Quincy, Massachusetts, Carlsbad and Asia. It hires manufacturing associates, automation and systems engineers, scientists, bioinformatics specialists, and sales and business development staff.

The Regulatory Operations Specialist is responsible for ensuring the efficient and compliant management of regulatory documentation, with a primary focus on Safety Data Sheets (SDS), product labeling, and SOP’s. This role is crucial in supporting global product compliance, ensuring that all documentation accurately reflects regulatory requirements and product specifications.

What You’ll Be Doing

  • Initiate, author, and maintain Safety Data Sheets (SDS) for all Twist products, ensuring 

compliance with global regulations.

  • Collaborate with cross-functional teams to obtain necessary product composition data and hazard

information for accurate SDS generation.

  • Manage the review, approval, and distribution of SDS to internal and external stakeholders.
  • Carries out duties in compliance with established business policies.
  • Perform day to day administration activities on EQMS as per approved procedures.
  • Work closely and collaborate with the Business Process Owner and EQMS users to develop and 

document configuration changes to meet business need

  • Perform other duties & projects as assigned.
  • Ability to travel 5%
  • Follow regulatory and ISO 13485 requirements.

What You’ll Bring to the Team

  • Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Biochemistry) or equivalent 

combination of education and work-related experience.

  • Working knowledge of medical device regulations, including ISO 13485 and EU IVDR (In Vitro Diagnostic Regulation); experience supporting regulatory documentation in an IVD or medical device environment strongly preferred.
  • 2 years of experience Regulatory Operations within a biotechnology, life sciences, or 

chemical manufacturing company or another Regulated Industry.

  • Expertise in developing technical documentation, including Safety Data Sheets (SDS), SOP, and 

work instructions

  • Familiarity with Quality Management Systems and electronic document control systems (eQMS)
  • Experience with Google Suite and/or MS Office Products required.
  • Experience with Master Control, Atlassian Confluence and/or JIRA preferred.
  • Strong written and oral communication skills (timely, clear, concise, accurate, conclusive, 

influential, targeted to audience) required.

  • Flexible, with ability to work effectively in a fast-paced, dynamic environment with shifting and 

competing demands is required

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