MSAT - Process Lead Technical Writer

Responsibilities

• Ensure Batch Records are consistently generated and delivered to Manufacturing in a timely manner, to a high level of quality, and with a high level of inter-departmental collaboration that ensures the promotion of Right-First-Time operations on the manufacturing floor.
• Adhere to established departmental practices and protocols and independently create new cGMP documents. Participates in editing documents and managing document comments. Maintains and reviews schedules.
• Perform daily work to support technical writing functions, including interacting with internal and external stakeholders/customers, hosting/attending ad hoc meetings and interceding on behalf of the team to resolve obstacles.
• Support other tasks as required, including Regulatory and Customer Audits, and participation in required reoccurring meetings.
• Oversee day-to-day activities, including assignment of work, to ensure compliant, timely completion of tasks including support the issuing of batch records, editing and peer reviews as required.

Requirements

• Bachelor's Degree required, Life Sciences area is preferred.
• Working experience of pharma/biotech (or equivalent) preferred.
• 5-10 years in a production environment.
• Working knowledge of GMP / Biotechnology manufacturing background referred, some experience in QA and/or Documentation creation preferred. Ability to manage multiple priorities.
• Technical writing in the biotech industry preferred.
• Project management skills required.
• Strong MS Word experience required.
• About Lonza
• Ready to shape the future of life science

Benefits

Additional Information

MSAT - Process Lead Technical Writer Location: On-site, Portsmouth, NH. The MSAT Process Lead Technical Writer is responsible for the development, revision, and delivery of high-quality manufacturing Batch Records and process documentation that support the production of life-changing therapies. The successful candidate will combine strong technical writing expertise with project management and cross-functional collaboration skills to ensure documentation is accurate, compliant, and delivered on schedule. This position plays a vital role in maintaining operational excellence, regulatory compliance, product quality, and ultimately patient safety. What you will get: Competitive salary and comprehensive benefits package. Opportunities for career development and advancement. Supportive and collaborative team environment. Access to cutting-edge technology and tools. Commitment to employee well-being and safety. Inclusive workplace culture. Recognition and reward for your contributions. Access to our full list of global benefits: https://www.lonza.com/careers/benefits

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