Sr Project Manager, Operations for Tris Pharma, Inc. to work at our Monmouth Junction, NJ loc. Lead + manage proj plans detailing milestones, bdgt, resources, timing + roles + responsibilities for prgms incl scale up activities, process validation, post validation changes + comm w/ FDA. Provide tech spt to manufacturing + packaging ops or other depts by leading proj w/ or

QC Lab Operations Specialists for Tris Pharma, Inc. to work at our Monmouth Junction, NJ loc. Perform duties to accord w/ company policies + procedures, SOPs, + state, federal + local laws. Test raw materials, In process, extended release Intermediates, Finished Product + Stability samples, incl dissolution, assay, preservatives, Related Compounds analysis, content/blend

The Manager, Quality Management Systems (QMS) supports, oversees and manages the Quality Assurance (QA) Investigations and Product Quality Complaints Team to ensure manufacturing quality controls and procedures are followed in accordance with Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs), Food and Drug Administration (FDA) standards an

Tris Pharma, Inc. (www.trispharma.com) is a leading privately owned U.S. biopharmaceutical company focusing on development and commercialization of innovative medicines addressing unmet patient needs. We have over 150 US and International patents including applications and several marketed branded and generic products in the U.S. We have licensed our products in the US an

Under supervision, performs laboratory analyses of raw materials, in process (IP), finished products (FP) and stability (ST) samples for pilot and submission batches, according to SOPs and cGMP procedures. Prepares method validation protocols/reports, and carries out method validation activities, including interim method validation, to meet project timelines. Supports lab

The Qualification Engineer supports and assists the Facilities & Engineering department with writing and execution of various qualification protocols for production and critical utilities equipment to meet production requirements including deadlines and compliance in accordance with Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs) and Foo

The Quality Assurance (QA) Research and Development (R&D) Senior Chemist takes a leadership role for other chemists on the QA R&D team in supporting Quality Control (QC) and Analytical R&D (AR&D) activities. These include but are not limited to method improvements, system equivalency, transfers, verifications, alternate source qualifications and authoring residual solvent

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

Tris Pharma, Inc. ( ) is a leading privately owned biopharmaceutical company in the U.S . with a mission to develop and commercialize innovative therapeutics that address unmet patient needs. Our core focus is CNS, with a marketed portfolio of best in class ADHD medicines and an exciting pipeline of clinical stage programs across Pain, Psychiatry, and Neurology. Our propr

The Manufacturing Technician is responsible for supporting and assisting in the production of a range of pharmaceutical products in accordance to Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs), Food and Drug Administration (FDA) standards and batch record specifications. She/he operates, sets up and maintains various pharmaceutical prod

Responsible for all aspects of HVAC and refrigeration equipment maintenance while complying with cGMPs, SOPs, and FDA requirements Performs routine and complex work related to troubleshooting, repair, and upgrade of HVAC and refrigeration equipment; Identifies, repairs, maintains, installs and/or replaces HVAC systems and equipment in order to ensure a proper and efficien

The Quality Assurance (QA) Research and Development (R&D) Analytical Chemist 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,

The Clinical Scientist supports clinical development programs by actively participating in, and/or leading when appropriate, aspects of the development, oversight and execution of phase I to IV clinical research trials. Collaborating closely with Physicians, Clinical Leaders and other scientific colleagues, the incumbent contributes to the design, data collection and repo

The Metrologist supports laboratory departments by performing routine calibration and instrument performance verification, maintenance and repairs on highly complicated instrumentation including, but not limited to High Pressure Liquid Chromatography/Ultra Performance Liquid Chromatography (HPLC/UPLC), Gas Chromatography (GC), ultra violet visible spectrophotometry (UV Vi

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 addressing 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