Development Scientist I

Catalent

8d • Onsite

About The Position

Development Scientist I
The Development Scientist I serves as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. This role is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation.
Position Summary
This position is 100% on-site at the Greenville 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 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 Development Scientist I will design, coordinate, and execute development and CTM activities, including formulation, data interpretation, equipment selection, generation of batch records and other appropriate documentation, and problem-solving exercises.

Requirements

• Bachelor’s degree in pharmaceutical science, chemistry, engineering, or related science with at least three years of industrial pharmaceutical experience required or;
• Master’s degree in pharmaceutical science or chemistry or related science with at least two years of industrial pharmaceutical experience required or;
• Ph.D. in Pharmaceutical Science or related field or Pharm.D. with at least one year of industrial pharmaceutical experience preferred.
• Some exposure to hazardous chemicals and other active chemical ingredients.
• Position requires the capacity to handle and manipulate objects using hands and arms.
• Requires ability to occasionally lift items in excess of 50 pounds.
• This position requires that a respirator be worn for your safety, and as such, employment is contingent upon being able to complete a medical evaluation with satisfactory results. The medical evaluation is conducted via an external vendor assigned by Catalent.

Responsibilities

• Independently design and execute experiments.
• Interpret data and make sound recommendations based on data.
• Solve formulation and process problems.
• Author SOP’s, IQ/OQ/PQ documents, development and technical reports, and CMC sections for regulatory submissions.
• Maintain competency and training for relevant processes and equipment.
• Ensure that all work is accurate, precise, properly documented, within GMP requirements.
• Organize multiple project responsibilities to ensure tasks are appropriately prioritized and executed on time.
• All other duties as assigned.

Benefits

• 152 hours of PTO + 8 paid holidays
• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees