Greenville, North Carolina, United States · On-site
Mid level$1.1B raised
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 packa…
Skills: Technical writing, Good Manufacturing Practice, Documentation management, Master Batch Records, Change control
Greenville, North Carolina, United States · On-site
$18/hr–$22/hr
Mid level
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Greenville, North Carolina, United States · On-site
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Greenville, North Carolina, United States · On-site
$30/hr–$43/hr
Mid level
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Greenville, North Carolina, United States · On-site
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Senior+
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Greenville, North Carolina, United States · On-site
$18/hr–$21/hr
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Greenville, North Carolina, United States · On-site
Entry level$1.1B raised
Sample Management Technician I Role About Site Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation deve…
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Greenville, North Carolina, United States · On-site
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Greenville, North Carolina, United States · On-site
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Greenville, North Carolina, United States · On-site
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Summary Responsible for the case management of the post-transplant renal patients. This position is designated as an on-site, patient-facing role. In-office presence is an essential function due to the need for real-time…
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Greenville, North Carolina, United States · On-site
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Greenville, North Carolina, United States · On-site
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Job Title: Registered Nurse I, Supervisor Department: Primary Care, Arlington FLSA Status: Non-exempt About us Physicians East, P.A.is a team of skilled healthcare professionals united to meet the challenge of delivering…
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Greenville, North Carolina, United States · On-site
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Greenville, North Carolina, United States · Hybrid
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Greenville, North Carolina, United States · On-site
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Greenville, North Carolina, United States · On-site
$34/hr–$46/hr
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Skills: Nursing, Patient assessment, Care planning, Interdisciplinary collaboration, Basic Life Support
Greenville, North Carolina, United States · On-site
Senior$20B raised
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Skills: Leadership, Pharmaceutical manufacturing, Manual visual inspection, cGMP, FDA compliance
Greenville, North Carolina, United States · On-site
$34/hr–$46/hr
Entry level
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Skills: Nursing Care, Patient Assessment, Care Planning, Interdisciplinary Collaboration, Patient Documentation
Greenville, North Carolina, United States · On-site
Mid level
Petco Veterinary Services offers relief veterinarians the chance to work in two distinct settings: Vetco Vaccination Clinics and Vetco Total Care full-service veterinary hospitals. In both environments, you'll have the o…
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Full-time
high school, associate degree, bachelor degree
Paid Time Off, Paid holidays, Medical insurance, Dental insurance, Vision insurance, Tuition reimbursement
Posted 19d ago
Apply by Sep 26
~40 hrs/week
Responsibilities
Collaborate with subject matter experts to create and update essential manufacturing documentation such as Master Batch Records and protocols. Support manufacturing and packaging activities by maintaining documentation systems, coordinating approvals, and assisting during audits.
Requirements
Requires a Bachelor's degree in a STEM field, or an Associate degree with 2 years of experience, or a high school diploma with 3 years of industry experience. Proficiency in GMP documentation and standard office software is essential.
Full 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 to join our team. In this role, you will work closely with subject matter experts to create and update essential documentation, ensuring accuracy and compliance. You will support manufacturing and packaging activities by maintaining documentation systems and coordinating approvals. This position offers the chance to contribute to cross-functional projects and play a key role in supporting audits and regulatory requirements.
Collaborate with subject matter experts to gather information for creating or updating documents such as Master Batch Records and protocols, and coordinate related change control documents
Review documents with subject matter experts and Operations personnel to ensure accuracy, executability, and consistent formatting
Maintain accuracy of the documentation database and ensure inputs meet company standards
Assist in making inputs to the Manufacturing Resource Planning system in preparation for manufacturing events
Close out help desk tickets related to document corrections and updates
Provide requested information during client and FDA audits
Participate in cross-functional project development team activities
Support the continued implementation of electronic document software systems
Coordinate document approvals across the organization
Respond quickly and effectively to changing priorities for multiple business units in packaging and manufacturing
The Candidate
Minimum Requirements
Bachelor’s degree in a STEM-related field; OR
Associate degree in a STEM-related field with at least 2 years of relevant experience; OR
High school diploma or equivalent with at least 3 years of relevant industry experience
At least one year of technical writing experience strongly preferred
Ability to administer quality system programs and resources
Familiarity with Good Manufacturing Practice documentation requirements
Proficiency with computer systems such as Microsoft Word, Excel, Adobe Professional, and database management software
Effective presentation and communication skills, as well as project and resource management skills
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 complete or earn a new degree
Engaging site-based activities such as Music Bingo, donation programs, and seasonal events
Employee Resource Groups promoting diversity and inclusion
Green initiatives and community engagement programs
Defined career path with annual performance reviews and growth opportunities
WellHub program supporting physical and mental wellness, including an 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.
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.
Championing the missions that matter™. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) and trusted partner to pharma, biotech, and consumer health companies worldwide. We put patients first in everything we do, helping people live better and healthier lives through every product we help develop, manufacture and deliver. With over 1,000 active development programs at any given time, we launch over 100 new products and line extensions annually. Catalent has supported half of all FDA approvals over the past decade, and our teams working at over 40 global sites help us produce over 60 billion doses every year.
Our strength lies in our people: teams across our more than 40 sites and thousands of passionate scientists and technicians who bring expertise in development sciences, delivery technologies, and multi-modality manufacturing. What unites us is our commitment to championing our partners’ missions as our own, anticipating customer needs, solving complex challenges and ultimately making a difference in the lives of patients across the globe.
At Catalent, you will be able to directly have an impact, solving problems and ensuring excellence for our customers. Our focus on delivering meaningful outcomes alongside our customers means your work directly impacts millions of people around the world. Join us in championing the missions that matter.
Catalent is headquartered in Tampa, Florida, with over 40 global sites. Visit www.catalent.com to learn more.
Offices: 101 E Kennedy Blvd, Tampa, Florida 33602, US · 14 Schoolhouse Road, Somerset, NJ 08873, US · Frankland Road, Blagrove, Swindon, Wiltshire SN5 8YG, GB · 4-9-17 Akasaka, Minato-ku, Tokyo 107-0052, JP · 160 Pharma Dr, Morrisville, NC 27560, US
How many Healthcare jobs are open in Greenville, NC right now?
There are currently 534 open healthcare positions in Greenville, NC listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Healthcare roles in Greenville, NC?
Companies currently hiring include ECU Health, Thermo Fisher Scientific, Physicians East, Grace Federal Solutions,LLC, Catalent, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Healthcare jobs in Greenville, NC?
Yes — 41 of the 534 open healthcare positions offer remote or hybrid work (17 remote, 24 hybrid).
How do I apply for Healthcare jobs in Greenville, NC?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.