Greenville, North Carolina, United States · On-site
About Site Catalent’s Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and p…
Skills: Technical Writing, GMP Documentation, Microsoft Word, Microsoft Excel, Adobe Professional
Fayetteville, North Carolina, United States · On-site
Current University of Arkansas System employees, including student employees and graduate assistants, need to log in to Workday via MyApps.Microsoft.com, then access Find Jobs from the Workday search bar to view and appl…
Skills: Diagnostic Assessments, Individual Therapy, Family Therapy, Group Therapy, Crisis Intervention
Fayetteville, North Carolina, United States · On-site
Current University of Arkansas System employees, including student employees and graduate assistants, need to log in to Workday via MyApps.Microsoft.com, then access Find Jobs from the Workday search bar to view and appl…
Skills: Diagnostic Assessments, Individual Therapy, Family Therapy, Group Therapy, Crisis Intervention
Concord, North Carolina, United States · On-site
$28/hr–$42/hr
Department: 11864 Atrium Health Cabarrus - Clinical Nutrition Status: Full time Benefits Eligible: Yes Hours Per Week: 40 Schedule Details/Additional Information: This position is Sign-on Bonus eligible. Based on eligibi…
Skills: Medical Nutrition Therapy, Nutritional Assessment, Patient Counseling, Clinical Documentation, Patient Education
Greenville, North Carolina, United States · On-site
Position Summary Pharmacists at ECU Health are committed to the safe and effective use of medications through maximizing drug distribution and optimizing drug therapy outcomes; educating patients, providers, and ourselve…
Skills: Medication Management, Pharmacokinetics, Drug Therapy Optimization, Patient Counseling, Medication Reconciliation
Durham, North Carolina, United States · On-site
Reliability Engineer Position Summary: Work Schedule: Monday - Friday, 8:00am to 5:00pm100% on-site The Morrisville (MSV) facility is Catalent’s center of excellence for nasal product development and manufacturing, provi…
Skills: Equipment Specification, Preventative Maintenance, CMMS, GMP, Project Management
Wilmington, North Carolina, United States · Remote OK
$111k–$213k/yr
Job Description SummaryAs a contributing member of the LOCA, Containment & Stability Analysis Team, you will perform safety analysis for plant thermal-hydraulic stability, plant noise, Power Range Neutron Monitor (PRNM) …
Skills: Thermal-Hydraulic Stability Analysis, Plant Noise Analysis, PRNM Stability Interface, Two-Phase Thermal Hydraulic Analysis, BWR Technology
Duplin County, North Carolina, United States · On-site
Performs a variety of quality and/or safety checks to ensure compliance with quality standards, reliability standards, and all specifications. Assists with troubleshooting and resolving quality issues through audits, sam…
Skills: Food Safety, Quality Assurance, GMP, HACCP, SOPs
Wilmington, North Carolina, United States · On-site
At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven r…
Skills: cGMP, SOP Compliance, Oral Solid Dosage Manufacturing, Microencapsulation, Blending
Morrisville, North Carolina, United States · On-site
Overview Metabolon is seeking a motivated and technically curious Technical Support Specialist to join a newly created post-sales technical support team supporting customers of Metabolon’s Verus LC/MS-based metabolomics …
Skills: LC-MS, Metabolomics, Analytical Chemistry, Sample Preparation, Bioinformatics
Hickory, North Carolina, United States · On-site
$143k–$197k/yr
Requisition Number: 76282 The company built on breakthroughs. Join us. Corning is one of the world’s leading innovators in glass, ceramic, and materials science. From the depths of the ocean to the farthest reaches of…
Skills: Automated Measurement, Machine Vision, Sensing Technologies, Systems Integration, Metrology
Durham, North Carolina, United States · Hybrid
$46k–$73k/yr
School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusi…
Skills: Project Management, Time Management, Interpersonal Skills, Written Communication, Verbal Communication
Durham, North Carolina, United States · On-site
$98k–$273k/yr
Position Summary We are seeking a Principal Statistical Programmer to provide full end‑to‑end statistical programming support across clinical development programs. This role requires deep technical expertise, leadership,…
Skills: SDTM, ADaM, TLF Development, Base SAS, Advanced SAS
Charlotte, North Carolina, United States · On-site
Department: 36399 Carolinas Medical Center - LCH: Radiology Xray Status: Part time Benefits Eligible: No Hours Per Week: 0 Schedule Details/Additional Information: PRN. Senior Radiography program student preferred. This …
Skills: Diagnostic X-rays, Patient Care, Radiation Safety, Medical Imaging, BLS
Charlotte, North Carolina, United States · On-site
Provide diagnostic quality radiographs for physicians and/or physician assistants while protecting employees and patients from unnecessary radiation and usage of appropriate protection standards. At OrthoCarolina, our te…
Skills: Medical Imaging, Medical Records Management, Patient Care, Radiography, Radiology
Wilmington, North Carolina, United States · Remote OK
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Country Approval Specialist – Make an Impact at the Forefront of Innovation! We have successfully supported the top 50 pharmac…
Skills: Regulatory Submissions, Local Regulatory Strategy, Informed Consent Form Negotiation, TMF Management, Site Activation
Charlotte, North Carolina, United States · On-site
The Asahi Kasei Group operates with a commitment of creating for tomorrow. Our business sectors, Material, Homes, and Health Care, contribute to the development of society by anticipating the changing needs of those arou…
Skills: Chemical Testing, Physical Testing, Resin Testing, ISO Certified Systems, MS Office
Charlotte, North Carolina, United States · On-site
The Asahi Kasei Group operates with a commitment of creating for tomorrow. Our business sectors, Material, Homes, and Health Care, contribute to the development of society by anticipating the changing needs of those arou…
Skills: Chemical Testing, Physical Testing, Resin Testing, DSC, TGA
Durham County, North Carolina, United States · Hybrid
California, US residents click here. The job details are as follows: Who We Are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purp…
Skills: Clinical Supply Chain Management, Vendor Management, IVRS/IWRS Systems, GCP, GMP
Durham County, North Carolina, United States · Remote OK
$183k–$270k/yr
California, US residents click here. The job details are as follows: Who We Are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purp…
Skills: Medical Monitoring, Clinical Development, ICH GCP, Protocol Review, Patient Safety
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The Technical Writer is responsible for authoring, formatting, and organizing technical documents such as Master Batch Records and protocols in collaboration with Subject Matter Experts. They also manage document databases, coordinate approvals, and provide necessary documentation during FDA and client audits.
Candidates must have a background in science, engineering, or industrial technology with experience ranging from one to three years depending on the level of education. Proficiency in Microsoft Office, Adobe Professional, and familiarity with GMP documentation requirements are essential.
Catalent’s Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development.
Technical Writer 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, Days.
100% based on-site in 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.
Requires a Bachelor’s degree in a science-related field, Engineering, or Industrial Technology, along with at least one year of relevant technical writing experience; OR Associate degree in a science-related field, Engineering, or Industrial Technology, with at least two year of relevant technical writing experience; OR High school diploma or equivalent with at least three year of relevant technical writing experience.
Individual may be required to sit, stand, walk regularly and occasionally lift up to 40 pounds.
Ability to administer quality system programs and resources.
Familiar with GMP documentation requirements.
Proficient with Microsoft Office Word and Excel and Adobe Professional.
Experience with database management software.
Positive and fast-paced working environment focused on continuous improvement and innovation
Competitive Paid Time Off plus 8 paid holidays
Medical, dental, and vision benefits effective from day one
Tuition reimbursement to support your educational goals
Engaging site-based activities such as NCAA Basketball Brackets, Golf Scrambles, and Onsite Pet Adoption Events
Employee Resource Groups promoting diversity and inclusion
Community engagement initiatives including Adopt-a-Highway clean-up
Defined career path with annual performance reviews and growth opportunities
WellHub program for physical and mental wellness
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 [email protected]. 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 [email protected] 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
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