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Regulatory Operations Specialist - Temporary

Twist BioscienceUSA Portland

Operations and administrationTemporary
Source-verified: read directly from this employer's own greenhouse job board, not a repost.Posted (1 month ago)Last verified (today)

At a glance

Location
USA Portland
Workplace
Not stated
Pay
Not published by the employer
Employment type
Temporary
Experience
Not stated
Education
Bachelor (or equivalent)
Job family
Operations and administration
Seniority
Not stated
Posted by employer
28 July 2026
Last verified open
7 September 2026
Team
Operations & Manufacturing
Listed via
Greenhouse

What the employer wrote

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

Where this record came from

Read from Twist Bioscience's own Greenhouse job board on , and last confirmed still open on . The employer published it on 28 July 2026. Jobsearch.ing did not write, edit or rank this posting, and does not vet the employer. View the original posting.

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