QMS Technical Writer and Document Control (Temporary)

August 21

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Twist Bioscience

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Synthetic DNA for Health & Sustainability

Synthetic Biology • DNA • Biotechnology • Drug Discovery • Gene Synthesis

501 - 1000

Description

• Responsible for creating high-quality written content for Quality Systems Integration Program • Daily interaction with technical documentation and attention to detail • Proofread, prepare, create, review, edit, and update various Quality and Technical Documents • Understand quality consequences from job performance and device defects

Requirements

• Bachelor’s degree in Business, Pharma, Tech, Biomedical or equivalent • Minimally 3 years of technical writing experience in a regulated industry • Experience in Quality Assurance/Regulatory requirements in medical devices • Experience and knowledge of Next Generation Sequencing and Synthetic Biology Manufacturing desirable • 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 required • Ability to work effectively in a fast-paced environment required

Benefits

• Bonus eligibility • Equity compensation • Generous benefits package • Final compensation varies by skill and location