Technical Writer, Document Specialist
1 week ago
At Lonza, we're dedicated to improving lives through innovative life sciences solutions. As a Technical Writer, you'll play a vital role in crafting high-quality documentation that meets the needs of our customers.
Main Responsibilities:
- Develop and revise Master Batch Records (MBRs) and other current Good Manufacturing Practice (cGMP) documents.
- Collaborate closely with Subject Matter Experts (SMEs) and customers to ensure documentation meets requirements.
- Produce high-quality documentation that meets applicable standards and requirements.
- Manage the lifecycle of MBRs, including creation, review, revision, and approval.
- Communicate actively with customers and address their comments and queries.
Requirements:
- Bachelor's degree in Engineering or Science related disciplines.
- Work experience in a cGMP regulated environment, preferably in biopharmaceutical processing.
- Strong technical communication and writing skills.
- Effective interaction skills with MSAT, MFG, QA, and customers.
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