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Regulatory Operations Specialist
Company | Twist Bioscience |
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Location | San Bruno, CA, USA |
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Salary | $31 – $42 |
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Type | Contract |
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Degrees | Bachelor’s |
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Experience Level | Junior, Mid Level |
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Requirements
- Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Biochemistry) or equivalent combination of education and work-related experience.
- Minimally 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.
- 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.
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.
Preferred Qualifications
- Experience with Master Control, Atlassian Confluence and/or JIRA preferred.