Chemist Salary at Zeolyst International BETA

Innospec Fuel Specialties is looking to add a Sr. Chemist to their fast-growing team in Newark, DE. Job Duties: Analyzes samples from various sources to provide information on different materials. Develops new techniques to analyze chemicals. Collaborates with specialists to interpret data and writes reports about the results. Analyzes test information to determine process efficiency and works on improvements. Plans, organizes, and performs scientific research projects in a particular scientific area. Capable to lead multiple projects in collaboration with business objectives. Prepares scientific reports or datasheets detailing the organization's products and their applications. Leads research teams in development of products. Proofread detailed technical reports. Prepare and deliver technical presentations on projects outside the research group. Job Requirements: Bachelor's degree in chemistry preferred 5-10 years of experience Analytical thinking skills Research skills 10% travel may

Senior Analytical Chemist – Malvern, PA Position Summary: The Senior Analytical Chemist will be involved in all phases of the production life cycle. This includes but is not limited to inspecting and evaluating raw materials, process samples and the releasing of finished products. This role accounts for validating and developing analytical methods to meet regulatory and customer requirements, preparing critical documentation, and performing data reviews to support product release. The Senior Analytical Chemist will also provide analytical support to the Process R&D group, recommend improvements to methods and procedures, and oversee the operation and maintenance of key laboratory equipment. This position demands a deep expertise in analytical techniques, method validation, and a proactive approach to problem-solving and process optimization. This position will directly report to the QC & Method Development Coordinator. Responsibilities :Conduct GMP analysis of raw materials, in-process

CHEMIST for ORGANICS SEMI-VOLATILES LABORATORY Build a Better Career Doing Purposeful Work! Would you like to join an award-winning, environmental testing laboratory where you can make a positive difference? Apply now with Suburban Testing Labs - STL where we live our mission every day to protect public health and preserve the environment. STL is a stable yet innovative company that's been successfully operating for over 60 years. We're a values-driven, environmental science lab where you won't just be a "number" -- you will be an integral part of our company with access to our executive leadership team. Our Chemists do important work that provides high quality, defensible data for our clients. In this role you’ll use state-of-the-art equipment & instruments to generate analytical data supporting environmental compliance and decision making. A key aspect of this position involves GC-MS testing (gas chromatography-mass spectrometry). Our compensation and benefits program includes: Compe

Innovative company is seeking an innovative and team-oriented surfactant and water treatment chemist in their facility located in the Philadelphia area. Chemist will be responsible for R&D projects covering a variety of formulation development and modification as well as leachate, condensate treatability study. The position will work closely with other R&D and QC Chemists as well as manufacturing technicians. This position will be located in West Chester, PA and report to the VP of Technology. Essential Functions & Responsibilities: Set-up internal standard test procedures New product development Leachate, condensate treatability study using various physical/chemical as well as biological processes. Scope, design and execute product performance improvement projects Formulation tailoring for unique customer specifications Operating bench scale or pilot scale leachate, condensate treatment systems Conduct water quality analysis. Support Manufacturing, Quality, Sales and Product Managemen

Job Description Job Description Wilmington PharmaTech (WPT) is seeking self-motivated Research Scientists to join our dynamic chemistry process department for active pharmaceutical ingredient (API) synthesis in clinical phase drug development. Key Responsibilities: Participates in the production of APIs in a kilolab or pilot plant setting by following batch records under cGMP environment. Records precisely all critical observations and documents all results during the production accurately. Diligently follows company SOPs to clean equipment for production and maintains appropriate cleaning records. Disassembles reactors for cleaning as necessary and reassembles them after the cleaning complete. Ensures and maintains kilolabs and related storage areas are in good condition. Performs routine qualifications for production equipment and maintains related records. Understands cGMP requirements of WPT and strictly follows all company policies, SOPs and best practices. Adheres to safety stand

Job Description Job Description Department Quality Control Job Title Chemist I FLSA Status Exempt 1. Role Purpose: The Quality Control (QC) Chemist I will be responsible to perform routine testing of incoming raw materials, packaging components, drug substances, in process samples, drug products, and stability samples in accordance with internal Methods of Analysis (MOA), compendial, and other test methods. Adherence to Standard Operating Procedures (SOP) and the United States Pharmacopoeia (USP) is required. Analytical techniques will include bulk/tapped density, pH, KF, titrations, dissolution, UV-VIS spectrophotometry, and other ancillary test methods, HPLC and other, as necessary. Attributable, legible, contemporaneous, original, and accurate documentation is also required. Work also needs to be completed in accordance with applicable FDA, OSHA, EPA, and DEA requirements. 2. Key Duties & Responsibilities: Performing routine analytical analysis of raw materials, packaging components

Job Description Job Description Candidates will design and perform experiments in order to develop new processes for the manufacture of new drug candidates. The candidate will be expected to subsequently undertake the manufacture of these drug processes at gram to kilo scale and support manufacture in pilot production as appropriate. An outstanding record of solving complex synthetic challenges combined with demonstrated hands-on ability to execute these processes at scale is required. This position requires a Ph.D. degree in Synthetic Organic Chemistry. The candidate needs to demonstrate a high level of technical ability, scientific creativity, teamwork and independence. Good communication skills are essential. Company Description Wilmington PharmaTech is a rapidly growing CRO/CMO serving the pharmaceutical industry. Company Description Wilmington PharmaTech is a rapidly growing CRO/CMO serving the pharmaceutical industry.

Quality Control Analytical Chemist II – Malvern, PA Responsibilities: Calibrate, maintain and operator laboratory equipment such as HPLC, GC, GC-HS, FTIR, pH meter, balances, KF, titrators and LCMS Conduct GMP analyses of raw materials, in-process materials, final product, and stability samples Complete GMP documentation needed to support release of raw materials, intermediates, and final products Validate methods for use in GMP environment Prepare documents such as methods of analysis, specifications, analytical reports etc. Provide analytical support to Process R&D (synthetic R&D) group and collaborate to advance the project Participate in method development and optimization as necessary Qualifications: Typically, BS w/ 3-5 years relevant experience or MS w/+2-year relevant experience in pharmaceutical industry. (or relevant fields) Previous QC/method development experience well considered Knowledge of cGMP regulations, USP, and chromatographic software is required. Excellent organiz