Tris Pharma, Inc. (www.trispharma.com) is a leading privately-owned biopharmaceutical company in the U.S. with a focus on development and commercialization of innovative medicines that address unmet patient needs. We have more than 150 US and International patents including applications and have marketed several branded and generic products in the U.S., have licensed our products in the US and international markets, and have a robust pipeline of innovative products spanning neuroscience and other therapeutic categories employing our proprietary science and technology.

Our science and technology make us unique, but it is our team members that set us apart; they are the engine that fuels Tris’ passion and innovation. Tris colleagues understand the criticality of operating a successful business and take pride in the company’s success. But of equal importance to each member of the team is how we interact with one another on a daily basis. We believe in each other and we believe in respectful, open and honest communications to help support individual and team success.

The Technical Writer supports the Operations department in the preparation/creation/modification of internal technical documentation. The incumbent disseminates technical information in easy-to-understand language to both technical and non-technical audiences. She/he will also assist other department designees in the preparation of appropriate concise and accurate technical internal documentation.

• Prepares and/or assists with the creation, writing and editing of internal documentation for the Operations group including but not limited to, SOPs, CAPAs, Customer Complaints, investigations and protocols; Updates Master Production and Manufacturing and Packaging Records and Component Specifications
• Understands and follows existing processes and procedures to create documentation which accurately records activities and recommends changes to streamline processes and actions
• Works collaboratively and cross functionally with internal departments (i.e., Technical Services, Quality Assurance, Scientific, etc.) for the delivery of effective and accurate written communication and documentation
• Participates in CAPA training and attendance at Report Review meetings, as needed
• Collaborates with subject matter experts (SMEs) and appropriate technical staff to create software documentation; Creates product manuals with screenshots and tutorials
• Observes Operations activities and processes to effectively support research and troubleshoot problems/issues as they arise

Minimum education and years of relevant work experience

Bachelors degree in a technical or scientific discipline ( Engineering, Chemistry, Biology, Physics, etc.)

Recent college graduations are encouraged to apply.

Special knowledge or skills needed and/or licenses or certificates required

• Ability to clearly and concisely organize and conceptualize complex technical information for non-technical and technical readers REQUIRED
• Potential to grasp technology quickly REQUIRED
• Strong writing and proofreading skills in a technical or scientific capacity REQUIRED
• Proficiency with Microsoft Office REQUIRED
• Familiarity and/or exposure to pharmaceutical manufacturing and production PLUS
• Current working knowledge of cGMPs in the pharmaceutical industry PLUS

Tris Pharma, Inc. offers a highly competitive compensation and benefits package. To build and enhance our diverse workforce, we encourage applications from individuals with disabilities, minorities, veterans, women, LGBTQ, etc. Tris Pharma, Inc. is an Equal Opportunity Employer. #LI-DNI