Lonza
MSATProcessTechnicalWriter
Neural analysis suggests this role is
optimal for Mid+ candidates.
“MSAT Process Technical Writer at Lonza. Skills: Process management, Technical writing, Document revision. Edit documents. Manage document revision”
What You'll Achieve.
Consistently delivering accurate and high-quality process Batch Records
What They're Looking For.
Must Have
Bachelor's degree required
Nice to Have
Working experience of pharmaiotech (or equivalent) preferred, Technical writing in the biotech industry preferred, MS Word experience preferred
What You'll Do.
Manage document revision
Manage document comments
Maintain and review schedules/campaigns
How You'll Work.
Team & Collaboration
Work with document owners; Support manufacturing
Communication Scope
Accurate, clear, and explicit description
Process & Methodology
Project management skills a plus
Full Job Description
**_MSAT Process Technical Writer_** ** _Location_** : On-site, Portsmouth, NH. An MSAT Process Technical Writer is responsible for consistently delivering accurate and high-quality process Batch Records to Manufacturing in a timely manner for a number of different customer projects. With a keen eye for precise and timely editing skills, Technical Writers accurately edit cGMP documents and maintain a busy documentation schedule. **What you will get:** * A collaborative and inclusive work environment. * Opportunities for career growth and development. * Access to cutting-edge technologies and tools. * Competitive compensation and benefits package. * 401(k) matching plan. * Supportive leadership and mentoring. * Commitment to ethical and sustainable practices. Access to our full list of global benefits: **What you will do:** * Edit documents: Review and template documents with accurate, clear, and explicit description and justifications. * Manage document revision: Perform initial review for scope, attain signoffs and justifications, set up review meetings, etc. * Manage document comments: Answer and translate questions into the reviewed document to meet regulatory, internal, and external requirements with the aid of document owners. * Maintain and review schedules/campaigns: Manage document timelines to support the manufacturing schedule; communicate and escalate appropriately to maintain document timelines. **What we are looking for:** * Bachelor's degree required (in Scientific related field is preferred). * Working experience of pharma/biotech (or equivalent) preferred. * Technical writing in the biotech industry preferred. * Project management skills a plus. * Strong MS Word experience preferred. * Position level and grade determined by level of experience. **About Lonza** At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core val
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