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. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations catalent.com . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE . 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.

Requirements

Must-haves

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

Nice-to-haves

Preferred Skill and Background

Application prep

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Keywords to mirror

agile

Platform: workday
Effort: long

Benefits

Benefits detected in the listing.

Dental

Vision

Paid Time Off

Wellness