USA - Portland, OR
2 months ago

Job Overview

Pay
Not disclosed

Job description

Location:
USA - Portland, OR, United States
Work arrangement:
On-site

Role Summary

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.

Responsibilities

  • ●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
Role:
Regulatory Operations Specialist - Temporary

Company profile

Twist Bioscience

twistbioscience.com

Twist Bioscience is a public synthetic biology company based in South San Francisco that manufactures synthetic DNA and DNA products for customers in a wide range of industries. Using silicon-based DNA synthesis, it makes gene synthesis products, oligo pools, exome and NGS target enrichment tools, variant libraries and other synthetic DNA tools for researchers across scientific disciplines. The company was founded in 2013 by Emily Leproust, Bill Banyai and Bill Peck.

Headquarters
San Francisco, California, United States
Founded
2013
Founders
Emily Leproust
Funding Stage
Public

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