Technical Writer

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’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation development through commercial manufacturing and packaging. The site specializes in oral solid dosage forms, supported by integrated formulation expertise, comprehensive analytical services, and scalable manufacturing capabilities designed to support both commercial products and potent or targeted therapies, including orphan drugs. Backed by more than $100 million in recent investments, the Greenville operation features fit‑for‑scale infrastructure, potent handling capabilities, and a strong regulatory track record, making it a critical part of Catalent’s global network for advancing complex oral drug programs from development to market.

Position Summary

We have an opportunity for a Technical Writer. This position is responsible for collecting, organizing, formatting and authoring documents. This role will make inputs into the site inventory management system for Manufacturing activities.

Shift: Monday- Friday 8:00am-5:00pm
Location: Greenville, NC
100% Onsite

The Role

• Work with Subject Matter Expert (SME) to gather the information needed to create new documents or updates of existing documents (i.e. Master Batch Records and protocols) and coordinate associated change control documents
• Review documents with SME and Operations personnel to ensure they are accurate, executable and the formatting is consistent and harmonized
• Ensure the documentation database is accurate, and inputs conform to company standards
• Ensure and assist in making inputs to the Manufacturing Resource Planning in preparation for manufacturing events
• Responsible to close out help desk tickets regarding document corrections and updates
• Provide requested information during client and FDA audits
• Participate and contribute to the activities of the cross functional project development teams
• Participate and contribute to the continued implementation of electronic document software system
• Coordinate document approval across the organization
• Provide lean and agile response to changing priorities in service of multiple business units for both packaging and manufacturing activities
• Other duties as assigned

The Candidate

Minimum Requirements

• Requires Bachelor’s degree in a STEM-related field with at least 1 year of relevant experience; OR
• Requires Associate degree in a STEM-related field with at least 2 years of relevant experience; OR
• Requires High school diploma or equivalent with at least 3 years of relevant industry experience
• Ability to administer quality system programs and resources
• Familiar with GMP documentation requirements
• Proficient with computer systems such as Microsoft Office Word, Excel and Adobe Professional and database management software
• Effective presentation/communication skills, project/resource management skills
• Position requires the ability to occasionally lift 40 lbs unassisted, and occasionally push and pull a maximum of 100 lbs
• Majority of workday is performed while sitting, standing, and walking
• Requires the use of hands for simple grasping and fine manipulations
• Ability to climb, bend, stoop, twist, and have full range of motion in upper and lower extremities
• Occasional exposure to dust, fumes, gases, skin and respiratory irritants, moving machinery parts, and damp, humid and wet environments

Preferred Skill and Background

• Strongly prefer at least one year of technical writing experience

Why You Should Join Catalent

• Positive and fast-paced working environment focusing on continual improvement and innovation.
• Competitive Paid Time Off plus 8 paid holidays.
• Medical, dental, and vision benefits effective day one of employment.
• Tuition Reimbursement to help you finish your degree or earn a new one.
• Engaging site-based activities such as Music Bingo, Puppy Supply Donation Program, and seasonal events.
• Employee Resource Groups promoting Diversity and Inclusion.
• Green initiatives and community engagement programs including highway clean-up.
• Defined career path with annual performance reviews and growth opportunities.
• WellHub program promoting physical and mental wellness, including onsite fitness center.
• Exclusive discounts through Perkspot from over 900 merchants.

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life‑saving and life‑enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Catalent is an Equal Opportunity Employer, including disability and veterans.

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Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.

Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.