QA R&D Chemist I

QA R&D Analytical Chemist, I Location: Monmouth Junction, New Jersey Summary The Quality Assurance (QA) Research and Development (R&D) Chemist I supports Quality Control (QC) and Analytical R&D (AR&D) activities by initiating appropriate change controls and updating specifications to reflect changes in methods. Analytical support activities include, but are not limited to: method improvements, system equivalency, transfers, verifications, alternate source qualifications and authoring residual solvent, elemental impurity and nitrosamine risk assessments, as directed by R&D. The incumbent may also perform additional responsibilities including laboratory analyses of raw materials, in-process (IP) testing, finished products (FP), stability (ST) sample testing and analytical instrumentation maintenance and calibration. Essential Functions Carries out responsibilities in accordance with company policies, Standard Operating Procedures (SOPs) and state, federal and local laws Creates, reviews or revises SOPs, methods, specifications, verification protocols, reports and change control requests, as needed; Performs vendor qualification for raw materials and packaging materials Performs testing of raw materials, packaging components, IP, FP and/or ST samples including dissolution, assay, related compounds analysis, content/blend uniformity, particle size distribution by Malvern/Sieve, bulk and Tap density, cleaning validation 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), UltraPerformance Liquid Chromatography (UPLC), Gas Chromatography (GC), Ultra Violet visible spectroscopy (UV/Vis), automatic titration, Infra-Red Spectroscopy (IR), Malvern Mastersizer, Thin Layer Chromatography (TLC) and dissolution apparatus (Distek) Collaborates closely with R&D for analytical method transfer studies and other analytical method related issues Assists with the identification and troubleshooting of problems with instrumentation and analytical preparations Authors Residual Solvent, Elemental Impurity and Nitrosamine risk assessments Meets project deadlines and performance standards, as assigned Maintains a clean and organized lab area Complies with all Company policies and procedures, including safety rules and regulations Adheres to GMPs and GDPs Any other QA R&D related tasks assigned by Supervisor or QA R&D Management Qualifications Minimum Education And Years Of Relevant Work Experience Bachelor’s degree in Chemistry or related science field and minimum 3 years lab experience in a cGMP related industry OR Master’s degree in Chemistry or related science field and minimum 1 year lab experience in a cGMP related industry. Special knowledge or skills needed and/or licenses or certificates required Hands on experience with analytical instrumentation (i.e., UV, IR, HPLC, UPLC, Malvern Mastersizer, GC and/or dissolution instruments) in a pharmaceutical, biotechnology or academic setting 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 Ability and willingness to work additional hours as required by business needs Preferred Qualifications Experience working with Food and Drug Administration (FDA), International Council on Harmonisation (ICH) guidelines, cGMPs and SOPs regulatory rules, regulations and guidelines Proficiency with Empower software and other laboratory software Experience with wet chemistry and chemistry related to sampling methods, quality control systems, analysis and documentation practices and procedures Prior experience working in a QC lab Travel Requirements 0% Physical Requirements Laboratory based position Ability to use Personal Protective Equipment (PPE) Ability to stand for extended periods of time Salary and Benefits Anticipated salary range: $85k – 95k. 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. Equal Opportunity Employer 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. #J-18808-Ljbffr