Scientist, Formulation R&D: Develop and optimize formulations for oral solid dosage forms (tablets, capsules, and modified release products). Conducting pre-formulation studies, excipient compatibility assessments, and dissolution profiling. Supporting analytical method development and validation for assay, dissolution, and stability- indicating methods. Design and execute stability studies as per ICH guidelines to establish product shelf life. Perform troubleshooting of formulation and analytical issues during development and scale-up. Collaborate with manufacturing and quality teams for pilot-scale and commercial-scale technology transfer. Prepare technical reports, development documents, and regulatory submission support (ANDA/CTD). Ensure strict adherence to cGMP, GLP, and regulatory requirements throughout the development process.
Requirements: Must have at least a Master’s degree in Pharmacy or Chemistry or Pharmaceutics, or related field. Must have 12 months of experience in the position or in a related position.
Salary: $117K - $120K per annum.
Hours: 40 hrs/wk 8:30am – 5:30pm
Location: Piscataway, NJ
Scientist, Formulation R&D • Piscataway, NJ, United States
Job Title: Clinical Lead, Early Clinical and Experimental TherapeuticsLocation: Cambridge, MA, Morristown, NJAbout the JobAre you ready to shape the future of medicine? The race is on to speed up d... Show more
If you have at least 5 full years of regional field monitoring, Provident Research is looking for you!This position will be working with a Provident Research Inc.Functional Source relationship.Inte... Show more
HORIBA US Life Science Field Leader.The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environm... Show more
Company DescriptionEurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our... Show more
Join Weiss-Aug A Leader in Precision Manufacturing and Innovation.Be part of a company that's shaping the future of manufacturing where your ideas, skills, and passion matter.Weiss-Aug, is a leadi... Show more
Ardena is a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO) specializing in precision medicine development.Ardena supports pharmaceutical ... Show more
The Research Study Manager oversees day-to-day clinical research operations across multiple oncology sites, ensuring high-quality execution of clinical trials, regulatory compliance, and effective ... Show more
Consultant Life Science ConsultingHybrid role:On-site in Cedar Knolls, NJ TuesdayThursday; remote Monday & FridayNuvera, now part of Inizio Engage, is a specialized consulting firm in the life ... Show more
Environmental ScientistJob ID15484# of Openings1Job LocationUS-NJ-ParsippanyCategoryEnvironmentalRelocation AssistanceNoService LineIESJob DescriptionDewberry is currently seeking an experienced En... Show more
We're here for one reason and one reason only to cure cancer.Every moment is dedicated to developing treatments and every action moves us one step closer to our goal.We've made incredible scientif... Show more
Computer System Validation Specialist.GxP application area Has working experience in any one or two of the following domains - clinical development and supply chain, drug discovery, MES, QMS, LIMS... Show more
Decision Intelligence Principal.Company Overview: Axtria is a global provider of data analytics, software, and consulting services for the Life Sciences and Pharmaceutical industry.With 3,700+ empl... Show more
Life Sciences Experience Design Strategy Senior Manager.Throughout the health ecosystem, you'll find courageous and inspiring people who are committed to driving transformation, advancing access to... Show more
Study Manager I, Extractable and Leachable.The Study Manager I, E&L will manage and coordinate projects for extractable and leachable (E&L) testing, including writing and reviewing study protocols ... Show more
Associate Director, Global Regulatory Sciences - Cmc.Those aren't words that are usually associated with a job.But working at Bristol Myers Squibb is anything but usual.Here, uniquely interesting w... Show more
Position Onsite Functional Area DescriptionThe Worldwide Patient Safety group is responsible for ensuring the safety of our medicines:The Worldwide Patient Safety group is responsible for pharmacov... Show more
SUMMARY OF POSITIONThe successful candidate will help in the clinical development of 505(b)(2) products and complex generics.The candidate should be able to act as an independent clinical pharmacol... Show more
Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts with national and international companies.We guarantee 15-25 hours per week with an hourly pay of bet... Show more
Location: Parsippany, NJ Type: Direct Hire - Full time permanent Compensation: $100,000.Work Model: Hybrid 2 days onsite, 3 days work from home.Lead analytical method transfers and validation acti... Show more
Work ScheduleFirst Shift (Days)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety StandardsJob DescriptionJoin us as a Scientist!At Thermo Fisher Scientific, you'll ... Show more
