QMS Technical Writer and Document Control at TWIST BIOSCIENCE CORPORATION

Portland, Oregon, United States -

Full Time

Start Date

Immediate

Expiry Date

25 Feb, 26

Salary

0.0

Posted On

27 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Technical Writing, Quality Assurance, Regulatory Requirements, Document Management Systems, Learning Management Systems, MS Office Products, Confluence, JIRA, Communication Skills, Attention to Detail, Training Development, Proofreading, Editing, Biotechnology, Gene Manufacturing, Synthetic Biology

Industry

Biotechnology Research

Description

The QMS Technical Writer is responsible for directly participating in a Quality Systems Integration Program, with primary responsibility being the creating of high-quality content. The Technical Writer will interact with individuals at multiple levels within all functional departments, including Quality Assurance, Regulatory Affairs, Supplier Quality, Supply Chain, Quality Control, Production, Process Development, Product Development, Software Development, R&D, Global Support in addition to building relationships with partners that manufacture products for the Wilsonville site. Key Responsibilities: Directly participate in a Quality Systems Integration Program, with the primary responsibility being the creation of high-quality written content and supporting Learning Management System. Daily interaction with technical documentation, with documentation tasks to be performed with quantitated high-throughput and attention to detail. Required to proofread, prepare, create, review, edit, and update Quality and Technical Documents including, but not limited to: SOPs, Design Control Documentation (Design and Development Plan, Customer Requirements, Product Requirements, Design Outputs, Design Verification Protocol and Reports), Technical Reports, Manufacturing Processes, Product Release, Materials Management, Post Market Surveillance, Quality Incidents, Complaint Handling, & CAPAs. Understands and is aware of the quality consequences which may occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities. Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices; build productive internal/external working relationships. Learn complex concepts and communicate the information in a way that is engaging and understood by users. Manage and update revision to technical literature. Maintain a comprehensive library of technical terminology and documentation. Oversight for updating Training Matrix/Plans. Meet with Managers to set up new or update current Training Plans. Build Training Curriculums. Learning Management System oversight. Provide New Hire overview training. Carries out duties in compliance with established business policies. Adapt rapidly to a changing industry and be able to adjust responsibilities, time and objectives accordingly. Perform other duties & projects as assigned. Ability to travel 10%. Qualifications Bachelor's degree in Chemistry, Biochemistry, Molecular Biology or related scientific discipline (Biomedical Engineering, or other related engineering field) or related field, or equivalent combination of education and work-related experience. 3-5 years of experience of technical writing experience in a GMP, Biotechnology, Pharmaceuticals or another Regulated Industry. Experience in Quality Assurance/Regulatory requirements in medical devices, IVD, EU IVDR/MDR, pharmaceuticals or biotechnology industry. Experience and knowledge of Next Generation Sequencing, Synthetic Biology Manufacturing, and Gene Manufacturing highly desirable Experience with document management systems required. Experience with Learning Management Systems. Experience with MS Office Products required. Experience with Atlassian Confluence and 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. About Twist Bioscience Twist Bioscience synthesizes genes from scratch, known as “writing” DNA. Just as children learn to both read and write, the next phase of development for the genomics revolution is the ability to write DNA. At Twist Bioscience, we work in service of people who are changing the world for the better. In fields such as health care, agriculture, industrial chemicals and data storage, our unique silicon-based DNA Synthesis Platform provides precision at a scale that is otherwise unavailable to our customers. Twist Bioscience Corporation is an Equal Opportunity Employer. Twist Bioscience Corporation provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic characteristics, or any other category protected by law.

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Responsibilities

The QMS Technical Writer is responsible for creating high-quality written content and supporting the Learning Management System as part of a Quality Systems Integration Program. This role involves daily interaction with technical documentation and requires attention to detail in proofreading, preparing, and updating various quality and technical documents.