Intern - Technical Services

Tris Pharma, Inc. (www.trispharma.com) is a leading privately-owned biopharmaceutical company located in Monmouth Junction, NJ. We focus on development and commercialization of innovative medicines that address unmet patient needs. We have >150 US and International patents and 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 and open, honest communications to help support individual and team success.

WHAT YOU WILL DO: 

We have an exciting Intern opportunity for a graduate student in our Technical Services department. Technical Services collaborates closely with, and provides direct validation support to, pharmaceutical development and manufacturing operations. This is a great opportunity to gain hands-on experience in a small, but productive, pharmaceutical department. It is a paid on-site assignment eligible for appropriate college credit (at school’s discretion) running approximately 6 mts. Work hours can be 24 -40 hrs/week 

Selected candidate will train with, and work closely alongside, Technical Services Engineers in assisting and supporting validation activities accurately and completing appropriate documentation fully and compliantly in accordance with current Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs) and Food and Drug Administration (FDA) requirements. 

WHAT YOUR TRAINING INCLUDES:

· Monitoring Batches and other engineering tasks on manufacturing floor following cGMPs

· Initiate Change Controls for batch records, procedures and policy updates

· Assist in issuance of protocols, batch records and coordinate with manufacturing for TS activities on the floor

· Assist in the upkeep of document databases, document scanning, filing and storages following Good Documentation Practices (GDPs)

· Assist in sample collections and transfers to appropriate labs for testing

· How to meet project deadlines and performance standards as assigned

· How to follow and comply with all Company, state and federal policies and procedures, including safety rules and regulations

REQUIREMENTS:

Open to Masters candidates in Pharmaceutical, Biomedical or Chemical Engineering or related scientific majors.

• Proficiency with Microsoft Office REQUIRED

• Verbal and written communication and skills REQUIRED

• Analytical thinking with problem-solving skills and the ability to adapt to changing priorities and deadlines REQUIRED

• Coachable, fast learner having a constant desire to advance skill set REQUIRED

• Strong training in, and understanding of, basic chemistry concepts REQUIRED

• Planning, organization and time management skills including the ability to support and prioritize multiple projects REQUIRED

· Prior exposure to pharmaceutical manufacturing and general knowledge of pharmaceutical manufacturing (tablet press, granulator, fluid bed processor etc.) PREFERRED

This is an Office and Manufacturing based position that will periodically require the use of Personal Protective Equipment (PPE). 

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