Summer Internship: Purification Intern… at BeOne Medicines · Hopewell

Summary: BeOne Medicines is a rapidly growing company focused on fighting cancer, and they are seeking a Drug Substance Purification Intern. The intern will gain hands-on experience in the pharmaceutical manufacturing process, including purification processes and compliance with regulatory standards. Responsibilities: - Acquire hands-on experience in adhering to Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and Good Documentation Practice (GDP) standards to maintain high-quality laboratory operations - Collect and organize information related to manufacturing - Conduct equipment testing and verification procedures to ensure accuracy and reliability in laboratory processes - Assist in red-lining of standard operating procedures and master batch records Required Qualifications: - Evidence of good verbal and written communication - Ability to work in fast paced dynamic environment with competing priorities - Demonstrated ability to collaborate within and between diverse groups - Proactive identification and implementation of continuous improvement opportunities - Able to receive and incorporate feedback – passion for ongoing professional development a plus - Aptitude for learning moderately complex technical systems - Must be able to stand for long periods, up to 8 to 12 hours/day - Must be able to reach above shoulder level, bend/stoop, push/pull, and handle/grip frequently - Must be able to work scheduled 40 hours with the ability to work overtime as needed - Must be comfortable in working in varying temperatures - Frequent lifting, pushing, pulling, and carrying. Ability to lift to 60 lbs - Regular reaching, bending, stooping, and twisting - Acquire hands-on experience in adhering to Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and Good Documentation Practice (GDP) standards to maintain high-quality laboratory operations - Collect and organize information related to manufacturing - Conduct equipment testing and verification procedures to ensure accuracy and reliability in laboratory processes - Assist in red-lining of standard operating procedures and master batch records - Microsoft Office applications Preferred Qualifications: - Enrolled in an undergraduate, graduate, or PhD program preferably in science, biochemistry, biotechnology, biology, chemical engineering and/or related discipline Required Skills: Laboratory Practice (GLP), Manufacturing Practice (GMP), Documentation Practice (GDP) Important Skills: Biochemistry, Biotechnology, Chemical Engineering Nice-to-Have Skills: Continuous Improvement, Technical Systems Learning, Microsoft Office Benefits: Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, Wellness