Manufacturing Specialist Intern

Alcami Corporation•Morrisville, NC

6d•Onsite

About The Position

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 regulatory track record. Are you interested in joining our team? Job Summary The Alcami Intern will complete company onboarding activities and provide feedback to ensure our onboarding program is efficient and engaging. Interns will develop their skills and increase their knowledge of CDMO regulations and activities while working in a world-class pharmaceutical environment. The Alcami Intern Program is a minimum 10-week paid program. Alcami interns are provided hands-on work experience building upon knowledge and skills learned in the classroom. Interns work side-by-side industry leaders in a dynamic, fast-paced environment who are passionate about being part of a team developing life-saving drugs around the world. The program concludes with individual presentations to Alcami leaders. On-Site Expectations 100% on-site position. 1st Shift: Monday - Friday, 7:00am - 4:30pm.

Requirements

Enrolled in a 4-year college or university pursuing a bachelor’s degree in Engineering, Life Sciences, or a field related to the internship.
Good verbal and written communication and documentation skills required.
Strong detail orientation and organizational skills required.
Good problem-solving and basic trouble-shooting ability required.
Willingness to collaborate with other team members.
Good knowledge of Microsoft Office including Word, Excel, and PowerPoint.
Follows all safety policies and leads by example a safety-first culture.
Produces high quality work products with a focus on first time right.
Complies with the company code of conduct, policies, and regulatory standards.

Responsibilities

Maintain inspection‑readiness binders with current SOPs, training records, and emergency contacts.
Assist Quality and Manufacturing Supervisors with completing batch record corrections.
Support continuous improvement efforts by identifying opportunities to update SOPs, defect libraries, batch documentation, and training processes, including simplifying procedural steps through documentation improvements.
Track and trend manufacturing activities to support process improvement.
Coordinate and source materials for hands‑on training activities (dispensing, compounding, filling, visual inspection).
Assist with organizing and maintaining in‑process and finished product samples, ensuring they are stored under the correct temperature‑controlled conditions (2–8°C, ‑20°C, ‑80°C).
Assist operators in vial/syringe manufacturing activities by preparing required materials and documentation.
Identify opportunities to improve training processes and simplify procedural steps through documentation updates.
Organize safety instrumentation information and calibration records.
Manage hazardous waste manifests and ensure return copies are received within 45 days.
Inventory, inspect, and restock spill kits as needed.
Perform AED inspections.
Participate in weekly safety walkthroughs and monthly warehouse walkthroughs.
The intern will complete all onboarding activities and provide feedback for process improvements.
The intern will be trained on proper techniques and documentation in a GMP environment. Techniques will depend on the group and area.
Interns will be trained on safety and quality expectations, and are expected to maintain safety and quality standards, and report safety observations according to company policy.
Upon completion of the internship, incumbents will conduct individual presentations to Alcami leaders.
Other duties as assigned.