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Regulatory Operations Specialist - Temporary

Twist Bioscience
Posted 2 months ago, valid for 11 days
Location

South San Francisco, CA, US

Salary

$31 - $42 per hour

Contract type

Full Time or Part Time

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Sonic Summary

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  • The Regulatory Operations Specialist is responsible for managing regulatory documentation, focusing on Safety Data Sheets (SDS), product labeling, and SOPs.
  • This role supports global product compliance by ensuring all documentation meets regulatory requirements and product specifications.
  • Candidates must have a Bachelor's degree in a scientific discipline and at least 2 years of experience in Regulatory Operations within a regulated industry.
  • The position requires expertise in developing technical documentation and familiarity with Quality Management Systems and electronic document control systems.
  • The base salary for this California-based role ranges from $31 to $42 USD per hour, with additional eligibility for bonuses, equity, and benefits.

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.
â—ŹCollaborate with cross-functional teams to obtain necessary product composition data and hazard
information for accurate SDS generation.
â—ŹManage the review, approval, and distribution of SDS to internal and external stakeholders.
â—ŹCarries out duties in compliance with established business policies.
â—ŹPerform 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
â—ŹPerform other duties & projects as assigned.
â—ŹAbility to travel 5%
â—ŹFollow 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.
â—ŹWorking 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
â—ŹFamiliarity with Quality Management Systems and electronic document control systems (eQMS)
â—ŹExperience with Google Suite and/or MS Office Products required.
â—ŹExperience 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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