AR&D Sr. Scientist I at Tris Pharma

South Brunswick, New Jersey, United States -

Full Time

Start Date

Immediate

Expiry Date

01 May, 26

Salary

135000.0

Posted On

31 Jan, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Method Development, Method Troubleshooting, Physical Characterization, HPLC, GC, UV/Vis Spectroscopy, IR Spectroscopy, TLC, ICP-MS, LC-MS, Dissolution Apparatus, Pre-formulation Studies, Reverse Engineering Studies, OOS/OOT Investigation, cGDP Compliance, Technical Report Writing

Industry

Pharmaceutical Manufacturing

Description

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 >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 our team members 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. Equally 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. Our AR&D lab is located in our Monmouth Junction, NJ headquarters has an immediate need for an experienced Analytical Research and Development Senior Scientist I Summary The Analytical Research and Development (AR&D) Senior Scientist I, under minimal guidance, performs analytical method development and troubleshooting of existing methods, designs and executes physical characterization studies to facilitate product understanding. Serving as analytical lead for assigned projects the incumbent provides analytical input to support complex technical investigations, guides highly specialized analytical tasks and conducts research on assigned problems and studies to support product development. She/he also prepares technical reports and other relevant scientific packages for internal and external use ESSENTIAL FUNCTIONS Primary duties/responsibilities · Carries out responsibilities in accordance with company policies, Standard Operating Procedures (SOPs) and state, federal and local laws · Acts as AR&D lead for assigned development projects liaising with Product Development (PD) department on analytical deliverables · Sets up and operates analytical instruments to support sample testing, including High Pressure Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultra Violet Visible spectroscopy (UV/Vis), Infrared Spectroscopy (IR), Thin Layer Chromatography (TLC), automatic titration, Inductively Coupled Plasma Mass Spectroscopy (ICP-MS), Liquid Chromatography–Mass Spectroscopy (LC-MS) and dissolution apparatus · Performs analytical method development and troubleshooting of existing analytical methods for in process (IP), finished products (FP) and stability (ST) sample testing; Performs and guides laboratory analyses of raw materials, IP, FP and ST samples · Designs and executes physical characterization studies to facilitate product understanding, such as rheological, microscopy, surface area and thermal studies · Designs, guides and performs reverse engineering studies of Reference Listed Drug (RLD) to support Product development · Designs, guides and performs pre-formulation studies (i.e, pH solubility, pH stability, excipients compatibility studies, etc.) in collaboration with PD · Performs trend analysis of development stability results, investigates Out of Specification (OOS) and Out of Trend (OOT) results in support of project directives · Provides analytical input to support complex technical investigations · Documents all testing details and results in laboratory notebooks compliant with current Good Documentation Practices (cGDPs); Prepares analytical method development reports, technical protocols/reports and scientific packages for internal and external use · Creates and reviews ARD SOPs, as needed · Safely and properly disposed of chemical waste, as needed · Cleans, maintains and calibrates laboratory instruments to ensure compliance with current Good Laboratory Practices (cGLPs) and current Good Manufacturing Practices (cGMPs); Cleans and organizes AR&D lab areas · Assists and trains lower level scientists · Performs related duties as assigned Requirements Requirements KNOWLEDGE/SKILLS/ABILITIES REQUIRED Minimum education and years of relevant work experience Bachelors degree in Chemistry or related science field and minimum 10 years experience in analytical development in the pharmaceutical or biotechnology industry OR Masters degree in Chemistry or related science field and minimum 8 years experience in analytical development in the pharmaceutical or biotechnology industry OR PhD in Chemistry or related science field and minimum 3 years experience in analytical development in the pharmaceutical or biotechnology industry. Special knowledge or skills needed and/or licenses or certificates required Strong knowledge and experience of physical characterization, thermal, spectroscopic and chromatographic techniques and concepts Hands on experience in setting up and operating multiple analytical instrumentation which may include: UV/Vis, HPLC, GC, TLC, ICP-MS and dissolution apparatus Strong working experience in designing and executing pre-formulation, analytical and physical characterization studies with high scientific standard Working knowledge of cGMP, Food and Drug Administration (FDA), Drug Enforcement Administration (DEA) and Occupational Safety and Health Administration (OSHA) regulations and guidance Strong technical writing skills, including SOPs, investigations, protocols, reports and scientific packages Ability to train and mentor lower levels scientist Proficiency with Microsoft Office Verbal and written communication and skills Ability to work independently and collaboratively, as required, in a fast paced, matrixed, team environment consisting of internal and external team members Analytical thinking with problem-solving skills and the ability to adapt to changing priorities and deadlines Planning, organization and time management skills including the ability to support and prioritize multiple projects Fluent in English (verbal and written) Ability to identify and distinguish colors Travel requirements 0% Physical requirements Laboratory based position Ability to lift up to 30 lbs Ability to use Personal Protective Equipment (PPE) Ability to stand for extended periods of time Anticipated salary range: $115k – 135k. Base salary offered is contingent on assessment of candidate’s education and experience level relative to requirements of the position and a review of related industry standards and internal equity. Additional benefits: In addition to base salary, full-time employees are also eligible for incentives, including, but not limited to: bonus eligible, medical, dental, vision, Rx insurance, 401K with match, life insurance, paid Company Holidays, PTO, Paid Volunteer Time and Employee Resource Groups. 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-_

Responsibilities

The Senior Scientist I performs analytical method development, troubleshooting, and designs physical characterization studies to advance product understanding, serving as the analytical lead for assigned projects. This role involves guiding specialized analytical tasks, conducting research, and preparing technical reports and scientific packages for internal and external use.