Intern - Quality Validation

Tolmar Careers•Windsor, CO

9h•Onsite

About The Position

Are you interested in learning new skills, exploring pharmaceutical research 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. About Tolmar Quality Validation Quality Validation is a key function in the pharmaceutical industry, focused on ensuring systems adhere to strict standards of quality, safety, and efficacy for our products, while also managing guidelines from the FDA and global regulatory bodies. Quality Validation involves systematic collaboration, planning, execution, and documentation of activities that demonstrate a company’s commitment to compliance with regulatory requirements and internal quality benchmarks. By validating systems—such as facilities, utilities, and equipment—Quality Validation helps protect the integrity of products, from raw material handling through to final packaging and distribution, ensuring systems perform their intended functions according to established specifications. Proposed Work Description The intern will be supporting the Quality Validation team. With coaching and direction from the team, specific activities could include, but are not limited to: Learn and support various pharmaceutical systems such as facilities, utilities, equipment, instruments, automated systems, and computerized systems Learn about system lifecycles and contribute to continuous improvement initiatives in validation practices Identify opportunities to improve company policies, procedures and facilitate recommendations Data entry and analysis in excel for: process improvements, refinements, and execution support Review validation supporting documentation and report packages Other duties as assigned

Requirements

Proficient computer skills with demonstrated knowledge in key Microsoft Office applications (Word, Excel, Project).
Strong communication skills and ability to work collaboratively and effectively in a team environment
Ability to work independently and efficiently
Ability to manage and prioritize multiple projects in a fast-paced environment
Effective organization and attention to detail
Willingness to maintain a regular and predictable work schedule, with some flexibility
Interest in the understanding of pharmaceutical systems and their lifecycle within a compliance and regulatory driven industry
Majoring in an engineering discipline (Chemical, Mechanical, Biomedical, Electrical and Computer Engineering) or closely related discipline.

Responsibilities

Learn and support various pharmaceutical systems such as facilities, utilities, equipment, instruments, automated systems, and computerized systems
Learn about system lifecycles and contribute to continuous improvement initiatives in validation practices
Identify opportunities to improve company policies, procedures and facilitate recommendations
Data entry and analysis in excel for: process improvements, refinements, and execution support
Review validation supporting documentation and report packages
Other duties as assigned