Associate Scientist

Catalent • Greenville, NC

10d • Onsite

About The Position

Associate Scientist The Associate Scientist serves as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. 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 Associate Scientist is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation. The Role Organize multiple responsibilities to ensure tasks are appropriately prioritized and executed on time. Assist in the design, coordination, and execution of development and CTM activities, including formulation, data interpretation, equipment selection, generation of batch records and other appropriate documentation, and problem-solving exercises. Ongoing communication with internal support groups, resources, vendors, staff, and occasionally clients. Support departmental and corporate objectives. All other duties as assigned.

Requirements

• Associate degree in Life Sciences field with at least two years of pharmaceutical experience required or; Bachelor’s degree in pharmaceutical-relevant field (e.g., Chemistry, Engineering, Pharmaceutical Sciences, etc.) required.
• 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.

Responsibilities

• Organize multiple responsibilities to ensure tasks are appropriately prioritized and executed on time.
• Assist in the design, coordination, and execution of development and CTM activities, including formulation, data interpretation, equipment selection, generation of batch records and other appropriate documentation, and problem-solving exercises.
• Ongoing communication with internal support groups, resources, vendors, staff, and occasionally clients.
• Support departmental and corporate objectives.
• 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
• Education Level: Associate degree
• Number of Employees: 5,001-10,000 employees