US Packaging Associate

Work Hours: Monday-Friday, 8am-5pm

Our major pharmaceutical client in Indianapolis is looking for an experienced US Packaging Associate to join their clinical trial supply management team.

They are seeking a detail-oriented and proactive team member to support key supply chain operations in collaboration with external vendors and internal systems. This role is integral to ensuring smooth material movements, accurate data management, & effective label inventory control.

A successful candidate for this role is quick to learn new computer programs & follow established processes to confirm/process packaging of pharmaceutical drugs for clinical trials around the globe. This person can communicate via email in a professional manner with internal & external customers. They are able to complete daily tasks independently, while also open to learning & supporting the team as time allows. This person is able to prioritize work effectively & is familiar with following a timeline.

Currently, this position is hybrid, with three days a week on campus. During training, some additional in-person days may be required. Due to the nature of the pandemic, the successful candidate should be open to both working more in-person days in the future as well as open to working completely remote if that is needed.

Daily responsibilities:

• Collaborate with external vendors and Collaboration Partners (CPs) to verify qualifications.
• Monitor bulk label stock inventory and initiate reorders as needed.
• Manage decommissioning and destruction of labels. Enter data into the deviation management system to address HUB carrier shipment issues
• Support temperature excursion (deviation) processes for designated CPs
• Coordinate material movements across systems and teams.
• Provide systems support for Trackwise, SAP, eCTS, ATLAS, and QualDocs.

Requirements:

• Eagerness to learn and adapt to new computer systems.
• Strong team collaboration skills with a focus on meeting shared goals and deadlines.
• Ability to prioritize tasks and manage urgent issues effectively.
• High attention to details and accuracy.
• Capability to work independently within established workflows.
• Flexibility to work both remotely and on-site.

Education requirement

• Bachelor's degree

Bonus

• A pharmaceutical or clinical trial experience/education a plus but not required.

Keywords provides a competitive compensation package, good benefits and a casual, fun, productive and supportive working environment. We empower people to perform to the best of their ability with our "can do" attitude. We appreciate and embrace flexibility and learn at every opportunity to grow ourselves through experience, training and tackling new challenges. This is what makes us Keywordians.

Benefits:

• Medical, dental and vision benefits
• Paid time off (including sick and select holidays)
• 401(k) enrollment with 3% employer matching

We are an equal opportunity employer & all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Keywords Studios is committed to fair & ethical hiring practices. We expect candidates to conduct themselves with honesty & to participate in all applications and interviews independently, presenting their own knowledge & experience. Candidates should refrain from using AI assistance or third-party tools or services that could influence, capture, or otherwise interfere with the authenticity of the assessment process.