Pharmaceutical Development Intern

Company: Disability Solutions
Location: Greenville
Posted on: February 1, 2025

Job Description:

Pharmaceutical Development InternPosition SummaryCatalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.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.The Pharmaceutical Development Intern role is an entry level, part-time role that will assist in project execution.Shifts: 20-28 hours/week.Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.The Role

• With close supervision support and assist in qualification of equipment
• With close supervision, assist in dispensing operations and assist in the development of timelines, Gantt charts and entry into MS Project,
• Become familiar with the QAD inventory system, and utilize system to dispense raw materials with close supervision, assist in the development of timelines, Gantt charts and entry into MS Project
• Research existing documents, and perform data entry and data analysis
• Execute experiment documentation such as protocols and manufacturing records
• With close supervision, assemble, disassemble, and clean and store equipment
• Ensure that all work is accurate, precise, properly documented, and compliant with SOPs and FDA cGMP guidelines
• All other duties as assigned.The Candidate
  • Current or recent enrollment in an undergraduate or graduate degree program (e.g. Chemistry, Chemical Engineering, Mechanical Engineering, or Pharmaceutical Science)
  • Must be located within 50 miles of the Greenville, North Carolina, site to be considered
  • Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds.
  • This position requires you to wear a respirator for your safety, and as such, employment is contingent upon you being able to complete a medical evaluation with satisfactory results prior to the start of your employment.Why You Should Join Catalent
    • Opportunities for professional and personal development & growth.
    • Several Employee Resource Groups focusing on D&I--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 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 . 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 .

Keywords: Disability Solutions, Wilmington , Pharmaceutical Development Intern, Healthcare , Greenville, North Carolina