Process Development Technical Writer I – Biologics

Catalent; Madison (WI); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical coverage

401(k)

Tuition reimbursement

Paid time off

Growth opportunities

Job summary

Catalent's Madison, Wisconsin site is seeking a Technical Writer I – Process Development to author, review, and maintain scientific and manufacturing documentation for cell line development and process development programs. The role emphasizes accuracy, clarity, and cross-functional collaboration to support client programs and internal operations.

The successful candidate will work with scientists and manufacturing teams, ensure GMP documentation practices, and contribute to continuous

Qualifications

• Bachelor's degree in a STEM discipline with a minimum of 1 year of relevant experience or an associate's degree with a minimum of 4 years of relevant experience.
• Strong written communication, editing, proofreading, and organizational skills.
• Proficiency with Word, Excel, and Outlook in Microsoft Office.

Responsibilities

• Author, edit, and maintain technical reports, protocols, certificates of testing, and other scientific documentation.
• Review documents for accuracy, consistency, completeness, and formatting.
• Collaborate with scientists, manufacturing personnel, quality teams, and SMEs to gather information and resolve questions.
• Identify discrepancies and escalate potential errors to ensure accurate reporting.

Skills

Technical writing

Editing

Attention to detail

Cross-functional collaboration

MS Office proficiency

Education

Bachelor's degree in STEM

Associate's degree in STEM

Tools

Microsoft Office

Job description

Catalent's Madison, Wisconsin site is seeking a Technical Writer I – Process Development to author, review, and maintain scientific and manufacturing documentation for cell line development and process development programs. The role emphasizes accuracy, clarity, and cross-functional collaboration to support client programs and internal operations.

The successful candidate will work with scientists and manufacturing teams, ensure GMP documentation practices, and contribute to continuous