MSAT Technical Writer

United States, Tampa (Florida)

MSAT Technical Writer

Location: Tampa, FL

Join our Manufacturing Sciences and Technology (MSAT) team and play a key role in supporting the production of high‑quality solid oral dosage (OSD) medicines. In this role, you will contribute directly to compliant, efficient, and reliable pharmaceutical manufacturing by developing and maintaining Master Batch Records (MBRs) that ensure process accuracy and regulatory compliance.

What You Will Get

A competitive compensation. In addition, below you will find a comprehensive summary of the benefits package we offer:

• Performance-related bonus.
• Medical, dental and vision insurance.
• 401(k) matching plan.
• Life insurance, as well as short-term and long-term disability insurance.
• Employee assistance programs.
• Paid time off (PTO).
  
  

Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

What You Will Do

• Create, edit, and format Master Batch Records (MBRs) for all OSD manufacturing stages, including dispensing, blending, granulation, compression, encapsulation, coating, printing and packaging
• Incorporate in‑process controls (IPCs), critical process parameters (CPPs), and yield calculations into compliant documentation.
• Maintain standard templates and provide training to supporting groups as needed.
• Ensure documentation complies with cGMP, FDA, EU guidelines, Good Documentation Practices (GDP), and internal formatting standards.
• Revise MBRs to reflect approved change controls, CAPAs, and process or workflow optimizations.
• Collaborate closely with MSAT Engineers, Formulation Scientists, and Production Supervisors to ensure technical accuracy and alignment with manufacturing processes.
• Suggest and implement continuous improvements to streamline documentation workflows and reduce errors while upholding all Safety and Sustainability expectations.
  
  

What We Are Looking For

• Bachelor’s degree in Life Sciences or a related field.
• Proficient experience in a cGMP pharmaceutical environment, strongly preferred within OSD manufacturing, QA, or documentation control.
• Proven ability to author clear, accurate, and compliant technical documentation.
• Strong understanding of cGMP requirements and regulatory expectations.
• Proficiency in Microsoft Word and general MS Office tools.
• Strong attention to detail, organization, and ability to collaborate with cross‑functional technical teams.
• Ability to adapt documentation based on process changes, data, and continuous improvement initiatives.
  
  

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 of 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.

Reference: R75390

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