About this role
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: https://www.lonza.com/careers/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 values—Collaboration, Accountability, Excellence, Passion, and Integrity—reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
Other facts
About Lonza
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
What you'll do
- The MSAT Process Technical Writer is responsible for delivering accurate and high-quality process Batch Records to Manufacturing. This includes editing documents, managing document revisions, and maintaining schedules to support manufacturing timelines.
Ready to join Lonza?
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