[ref. e0089922] Summer Intern - Analytical Chemistry

Role Overview & Key Functions::

We hire exceptional people and trust each other to work in whatever way lets us, be us – whether that’s onsite, from home, or anywhere in between.

Our summer intern program, which will run from May 27th – Aug 8th, allows students to gain real world work experience in a high energy, collaborative work culture.

This role will gain insight into analytical oversight as a sponsor for vendor management collaborating remotely with our third-party manufacturers. In addition, you will contribute to organizing data to facilitate analytical oversight, align third-party review processes, and support regulatory readiness.

• Support FDA data readiness and organization of XPOVIO® products and annual regulatory submission, including gap assessments for completed studies
• Manage and organize analytical-related documents such as raw data, Certificate of Analysis (COAs), and reports
• Interface with third-party vendors to align analytical programs that support manufacturing and stability
• Collaborate with Analytical and GMP Quality team members to assist in KPTI stability programs review process
• Assist in site evaluations to support ongoing Failure Modes and Effects Analysis (FMEA) initiatives aimed at reducing data review time within the Analytical Team
• Participate in weekly telecons and cross-functional team meetings with external manufacturing sites and internal program teams

Candidate Profile & Requirements::

• Currently enrolled in a full-time chemistry or pharmaceutical sciences degree program with some pharmaceutical testing experience
• Strong communication and time management skills capable of working independently and cross-functionally in a remote work environment
• Strong organization skills with the ability to handle multiple projects simultaneously and effectively
• Proficiency with Microsoft Office including Word, Excel, PowerPoint, Teams
• Analytical or quality control experience in small or large molecules or oral drug products a plus for exposure to different types of data
• Familiar with a variety of analytical testing such as HPLC, GC, Dissolution, FTIR, UV/Vis, Karl Fisher titration, etc.
• Familiar with data analytics and trending including excel for graphing and hyperlinking source documents
• Interest in understanding FDA regulatory commitments in commercial programs
• Familiar with cGMP, USP, FDA, and ICH requirements a plus
• You have a strong interest in life sciences and are passionate about giving patients with cancer a chance to enjoy more of life’s precious moments.
• You feel a strong connection with our ICARE values (Innovation, Courage, Alignment & Accountability, Resilience, and Energy)
• You demonstrate enthusiasm for learning and a commitment to career development

Our Value Proposition::

At Karyopharm, we live and demonstrate our ICARE values every day! Check out our Culture Video!