Intern - Supplier Quality

Tolmar Careers•Fort Collins, CO

14h•$19•Onsite

About The Position

Are you interested in learning new skills, exploring pharmaceutical research, quality and manufacturing, networking with experts, and building a resume that opens doors? Join us to jumpstart your career! At Tolmar, you will connect with like-minded professionals in a supportive community. This is a place where you can make a meaningful impact and feel empowered by the abundant opportunities for growth. Tolmar, Inc. is a fully integrated pharmaceutical company based in Colorado. We develop, manufacture, and distribute both branded and generic prescription medications globally, focusing on oncology, urology, and pediatric endocrinology. Our long-acting injectables and oral medications offer innovative treatment options that meet the diverse needs of patients worldwide. By leveraging emerging technologies and developing new products, we aim to simplify treatment delivery and enhance the overall patient experience. The Supplier Quality department assists with ensuring the quality of the materials and products sourced by Tolmar to produce drug products meets all internal and global requirements. This includes assuring the systems in place for selecting, approving, managing and requalifying suppliers comply with applicable guidelines and regulations established by the FDA and other global regulatory bodies. Supplier Quality is an important aspect of quality assurance. The intern will be supporting the Supplier Quality team. With coaching and direction from the team, specific activities could include, but are not limited to: Updating standard operating procedures (SOPs) and work instructions (WIs) including formatting them per company procedures and routing for approval in the company’s electronic document management system (EDMS). Requalification of suppliers. Investigating potential impact of Supplier Change Notifications to Tolmar products. Working globally with suppliers on Supplier Corrective Action Requests (SCARs) to confirm that suppliers are implementing corrective and preventive actions when non-conforming purchased product is identified. Other duties as assigned.

Requirements

Proficient computer skills with demonstrated knowledge in key Microsoft Office applications (Word, Excel, PowerPoint).
Effective organization and attention to detail.
Willingness to maintain a regular and predictable work schedule, with some flexibility.
Effective oral and written communication.
Ability to interact collaboratively and effectively in a team environment.
Ability to work independently
Majoring in an engineering discipline (Biomedical, Chemical or Mechanical Engineering) or closely related discipline.

Nice To Haves

Familiarity with Software systems and understanding is a plus but not required.

Responsibilities

Updating standard operating procedures (SOPs) and work instructions (WIs) including formatting them per company procedures and routing for approval in the company’s electronic document management system (EDMS).
Requalification of suppliers.
Investigating potential impact of Supplier Change Notifications to Tolmar products.
Working globally with suppliers on Supplier Corrective Action Requests (SCARs) to confirm that suppliers are implementing corrective and preventive actions when non-conforming purchased product is identified.
Other duties as assigned.