Associate QC Analytical Chemist

Description

Tris Pharma, Inc. (www.trispharma.com) is a leading privately-owned U.S. biopharmaceutical company with a focus on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs. We have more >150 US and International patents and market several branded ADHD products in the U.S. We also license our products in the US and ex-US markets. We 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 fueling Tris' passion and innovation. Our colleagues understand the criticality of operating a successful business and take pride in the company's success. But of equal importance to each team member is how we interact with one another on a daily basis. We believe in each other and in respectful, open and honest communications to help support individual and team success.

We have an immediate opening in our Monmouth Junction, NJ QC Lab for an (Associate) QC Analytical Chemist. This is an entry level scientific position and we will train qualified candidates who meet listed requirements. Recent college graduates are welcome to apply.

The (Associate) Quality Control (QC) Analytical Chemist performs analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), and/or stability samples (ST). She/he is also responsible for following Analytical Methods, current Good Manufacturing Practices (cGMPs), Protocols, Standard Operating Procedures (SOPs) and company policies.

• Carries out responsibilities in accordance with the organization's policies, SOPs, and state, federal and local laws
• Performs testing of raw materials, IP, FP and/or ST samples including dissolution, assay, content/blend uniformity, particle size distribution, and other tests according to the analytical methods, United States Pharmacopeia (USP) procedures in a regulated laboratory environment
• Analyzes and interprets test results
• Operates general analytical instruments during raw material, IP and FP testing such as High-Pressure Liquid Chromatography (HPLC), Ultra Violet visible spectroscopy (UV/Vis), Automatic Titration, Infra-Red Spectroscopy (IR), Atomic Absorption (AA), Thin Layer Chromatography (TLC) and Dissolution apparatus (distek)
• Assists with the identification and troubleshooting of problems with instrumentation and analytical preparations
• Meets project deadlines and performance standards as assigned
• Complies with all Company policies and procedures, including safety rules and regulations

Requirements

Bachelors in Chemistry or related scientific field AND 0-3 years hands-on lab experience in a pharmaceutical, biotechnology or university laboratory REQUIRED.

* Proficiency with Microsoft Office REQUIRED

* Excellent verbal and written communication and skills REQUIRED

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

* Coachable, fast learner with a constant desire to advance skill set REQUIRED

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

* Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects REQUIRED

* Ability and willingness to work additional hours as required by business needs REQUIRED

* Hands-on experience with analytical instrumentation (UV, IR, HPLC, and/or dissolution instruments) in a pharmaceutical, biotechnology or academic setting a 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