Intern - Process Engineering

Tolmar Careers•Windsor, CO

9d•$19

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 Process Engineering The Process Engineering team is the process design and support arm of MS&T (Materials Science & Technology) and is tasked with providing engineering expertise for our commercial and development products. Some of the tasks Process Engineering is responsible for includes scale-up and lifecycle management changes for commercial products/processes as well as support of any changes in process equipment or raw materials/excipients or components as well as providing input into the process and product design of new products in the Tolmar pipeline. The Process Engineering team has responsibilities that create a challenging, yet extremely rewarding fast-paced work environment. Proposed Work Description The nature of business is that priorities can shift according to the needs of the company/department and therefore the work described below is a sampling of the kinds of work we expect this position to entail: Work with Process Engineers to design experiments, collect and analyze data to support changes to processes or product materials/excipients. Assist with general engineering tasks such as reviewing notebooks and data. Learn and apply cGMP documentation practices within a pharmaceutical environment. Additional duties may be assigned based on department needs. Potential travel between Fort Collins and Windsor, reimbursable.

Requirements

Basic knowledge of laboratory or manufacturing principles and procedures.
Good documentation skills.
Attention to detail.
Ability to learn and understand complex systems.
Effective verbal and written communication.
Willingness to maintain a regular and predictable work schedule
Proficiency with all Microsoft Office applications.
Ability to work independently as well as co-operatively within a team environment.
Pursuing a degree in Chemical or Biomedical Engineering, Chemistry, Biology, or related field.
Have achieved an overall cumulative GPA of 3.0 (on a 4.0 scale) or higher.

Nice To Haves

Exposure to or coursework covering process design.
Knowledge of Pharmaceutical development and Current Good Manufacturing Practices (CGMP) with interest in the pharmaceutical industry preferred.

Responsibilities

Work with Process Engineers to design experiments, collect and analyze data to support changes to processes or product materials/excipients.
Assist with general engineering tasks such as reviewing notebooks and data.
Learn and apply cGMP documentation practices within a pharmaceutical environment.
Additional duties may be assigned based on department needs.
Potential travel between Fort Collins and Windsor, reimbursable.