GMP Technical Writer – Onsite Documentation

Catalent Pharma Solutions; South Carolina; On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical, dental, and vision benefits

Tuition Reimbursement

Paid time off and holidays

Job summary

Catalent is seeking a Technical Writer to collect, organize, format, and author documents for manufacturing activities at Greenville, NC. You will input data into the site inventory system and support change controls, audits, and cross‑functional projects.

The role emphasizes GMP documentation, MS Word/Excel proficiency, and effective communication in an onsite environment. A STEM degree with experience is required.

Qualifications

• Requires STEM degree with 1+ year relevant experience or an equivalent combination.
• Familiar with GMP documentation requirements and quality systems.
• Proficient in MS Word, Excel and Adobe Professional; basic database management skills.
• Strong written and verbal communication; project coordination abilities.
• Able to lift up to 40 lbs and operate in an on-site environment.

Responsibilities

• Collaborate with SME to create or update documents like Master Batch Records and protocols.
• Review documents for accuracy, consistency and formatting alignment.
• Maintain documentation database and ensure inputs meet standards.
• Assist in input to Manufacturing Resource Planning for events.
• Resolve document corrections via help desk tickets; support audits.

Skills

Technical writing

GMP documentation knowledge

Microsoft Office

Cross-functional collaboration

Strong communication

Education

Bachelor’s degree in STEM

Associate degree in STEM

High school diploma with experience

Tools

Microsoft Word

Excel

Adobe Acrobat

Database management software

Job description

Catalent is seeking a Technical Writer to collect, organize, format, and author documents for manufacturing activities at Greenville, NC. You will input data into the site inventory system and support change controls, audits, and cross‑functional projects.

The role emphasizes GMP documentation, MS Word/Excel proficiency, and effective communication in an onsite environment. A STEM degree with experience is required.