Chemist Salary at Pharmaceuticals Llc BETA

Seeking a Quality Control Chemist to join a Pharmaceutical company near Glassboro, NJ. Only local candidates will be considered. SUMMARY: The incumbent demonstrates proficiency through a wide exposure to pharmaceutical analyses and has a firm grasp of scientific principles and skill in applying this knowledge. The incumbent has practical experience in pharmaceutical analyses and routinely performs analysis in two of the functional areas (HPLC, GC, or Wet Chemistry). The incumbent performs and trains on routine chromatographic analyses. The incumbent works independently. ESSENTIAL DUTIES AND RESPONSIBILITIES: Provides analytical support for production. Performs GC, HPLC and/or Wet chemistry analyses on Raw Material, In-process and Finished Lot samples. Supports Analytical and Chemical Development by testing samples. Provides quick turnaround of In-process samples to production. Thoroughly documents all results in a laboratory notebook as well as compile all data into an ancillary. Empti

Job Title: Chemist Department: Quality Control Location: New Brunswick, NJ SUMMARY: This position is responsible for performing various laboratory tests to determine chemical and physical characteristics or composition of solid or liquid materials. Laboratory tests will primarily include wet chemistry and may include basic use of instrumentation such as Gas Chromatography and High Pressure Liquid Chromatography. The Chemist I will also be responsible for supporting the Quality Control laboratory through reagent compounding. This position will also be responsible for performing identification testing using wet chemistry or instrumentation analysis, physical property testing and general laboratory upkeep. The individual will also be responsible for maintaining a laboratory notebook in accordance with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP). ESSENTIAL DUTIES AND RESPONSIBILITIES: Performs tests on a wide variety of samples of manufactured products to veri

Chemist III—New Brunswick, NJ Job Summary Perform analytical testing drug products such as tablets and capsules and liquid products. Operate instruments such as HPLC, GC, Dissolution, Particle size, KF titrator. Perform method transfer and validation. Calibration of analytical instruments. Area Of Responsibility Performs routine analytical tests of pharmaceutical raw materials, in-process samples, blends, finished products, and stability samples using instrumentation such as HPLC, UPLC, GC, UV/VIS, FTIR, dissolution apparatus, particle size analyze, etc. Timely complete the laboratory training. Complete the assign task as schedule and complete the laboratory documentation contemporaneously. Legible and accurate documentation of all the raw data, observations in the worksheets/templates/notebooks. Perform QC testing of exhibit batches Perform the testing of process validation/characterization batches and stability samples. Compile the analytical data and notify the results to supervisor

Our client, a skincare brand, is looking to hire a Senior Chemist to join the team at their corporate office onsite in Edison. Candidates must be able to work a 5 day, in office schedule. Job Duties Include: Lead reformulation initiatives to enhance product performance, stability, and to ensure alignment with regulatory and market demands Develop skin, hair, and body care formulations that prioritize technical excellence, consumer appeal, and market relevance Serve as the technical lead on cross-functional projects, facilitating communication between R&D, Regulatory, QC, and Manufacturing teams Troubleshoot and resolve technical challenges related to stability, viscosity, pH, compatibility, and texture to meet quality and performance standards Collaborate to transform concepts into feasible, trend-driven products Scale formulations from bench prototypes to pilot and full-scale manufacturing Oversee stability testing and analyze results to ensure formula integrity across varying conditi

We’re seeking an experienced Senior Scientist/Head Chemist with proven expertise in formulation development, troubleshooting, and innovation across skin care, hair care, and body care. In this role, you’ll work closely with Marketing, Product Development, and Manufacturing to deliver high-performance, market-ready products that align with consumer trends and business goals. The Role In this role, you will be responsible for: Developing innovative formulations for skin care, hair care, and body care, ensuring technical excellence, consumer appeal, and market relevance. Leading reformulation efforts to optimize product performance, improve stability, and align with regulatory or market needs. Troubleshooting technical issues related to stability, viscosity, pH, compatibility, and texture, delivering solutions that meet quality and performance standards. Collaborating with Marketing and Product Development to translate concepts into viable, on-trend products. Scaling up formulations from

Details: Pay for this position is 28.00 to 31.43 hourly depending on experience. This position is a one-year contract with the possibility of extension or conversion to permanent. Location: Branchburg, NJ Hours: 7:00 am to 3:30 pm Qualifications: BS in Chemistry, Physics, or related Scientific discipline 3 + years of related industrial experience in QC environment QC analytical chemistry experience is required. Experience with chromatographic (GC, HPLC, GPC) and spectroscopic instruments. Experience in a cleanroom environment. Preferred, but not required experience: ICP-MS systems, GFAA, OES-ICP, Method development. Summary You will join the QC Analytical/Metals group for the analysis lithography chemicals and other formulations used in the semiconductor fabrication industry. This is a hands-on role with 80% of time spent in the lab. Performs routine and non-routine sample analysis Conducts hands-on laboratory work Operate and maintain analytical equipment Provides analytical and troub

Summary: QC Chemist: This position’s purpose is to support the Quality Control lab for analysis of purified water, raw materials, finished and stability samples. Essential Duties and Responsibilities: QC Chemist Sample of Raw materials and Purified water for Analysis Arrange retain samples for raw materials and finished products Performing daily analytical balance verification- as required Performing calibration of pH meters and Fluoride Ion meters as required Preparation and standardization of Volumetric solutions and test solutions as required Arranging chemicals in the lab and checking for their expiration dates as required Arranging quality control documents as needed as required Performing wet analysis for raw materials and finished products, which includes Loss on drying, Viscosity, pH and water content etc. Performing chart replacement for all chart records which monitor temperature and humidity as required. Perform analysis using HPLC/UV-Visible spectrophotometer for raw materi

Job Description Research Chemist - Chromatography - Whitehouse, New Jersey Intertek Pharmaceutical Services located in Whitehouse, New Jersey, USA, is a cGMP contract testing, analytical research and development laboratory. Intertek Pharmaceutical Services works directly with both large and small pharmaceutical companies to help bring safe and effective pharmaceutical products to market. An opportunity has arisen for a Research Chemist to join this organization focused on chromatographic method development, validation and oversight of method performance. Intertek's Chemical & Pharmaceuticals team brings quality and safety to life through regulatory guidance and supply chain assurance to support your unique pharmaceutical or biopharmaceutical outsourcing requirements. Over the last 20 years, our network of laboratories and regulatory experts have provided high quality custom pharmaceutical services ensuring Total Quality Assurance for some of the world's largest and most innovative phar