QC Chemist Salary at Dmi/ Canterbury Corp BETA

QC Chemist Job Title: Quality Control Laboratory Chemist – Radiopharmaceuticals Evergreen Theragnostics, Inc. is a radiopharmaceutical company headquartered in Springfield, NJ. We operate in a brand-new state-of-the-art facility, developing our own radiopharmaceutical products and providing contract development and manufacturing services for other radiopharmaceutical companies. We also operate our own cutting edge cancer research laboratories. Evergreen is a small team, where all team members support each other in a variety of activities. We are looking for team members who are motivated to take on new challenges and excited to help build the company. Job Description: We are seeking a highly skilled and experienced Quality Control Laboratory Chemist to join our team in the Radiopharmaceuticals division. This critical role involves the quality control processes documentation development, analytical methods improvement, and ensuring compliance with regulatory standards. The ideal candida

Job Description Our Linden, NJ Facility is Looking for a Lab Chemist I (Internship), they will beresponsible for sample preparation, the analysis of samples to determine their chemical and physical properties. This is a traditional, white lab coat position that offers no travel and a flexible schedule! We are looking for an experienced individual with good work ethic. Pay: $19.50 Shift: 1st Duration: May - Sept Why work for Clean Harbors? Health and Safety is our #1 priority and we live it 3-6-5! Competitive wages Comprehensive health benefits coverage after 30 days of full-time employment Generous paid time off, company paid training and tuition reimbursement Positive and safe work environments Opportunities for growth and development for all the stages of your career Responsibilities Key Responsibilities: Ensures Health and Safety is the number one goal by following policies, processes, and acting in a safe manner at all times. Responsible for maintaining a safe working environment t

Division Overview: Aurolife was founded in 2008 as part of a group of companies that has a long history of excelling in generic pharmaceutical prouct development and manufacturing. Aurolife has a 10 year history of extraordinary manufacturing practices in the solid oral dose arena. The support and expertise of our parent organization has given Aurolife a jump start in building a solid pharmaceutical portfolio very quickly. The Aurolife family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality control and regulatory affairs. In addition to several formulations under manufacture, we have a robust pipeline of products. Aurolife's aim is to provide healthcare at economical prices to make this a healthier world to live in. Job Overview: The Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist will work as a member of team to effectively plan and QC an

Chemist- South Plainfield, NJ Key Responsibilities: Prepare samples of OTC drug, pharmaceutical products per established methods. Conduct basic chemical analyses using laboratory instruments such as IR, UV, dissolution, viscosity, melting point, and other equipment. Perform HPLC and/or GC quantitative analysis Report data from methods and instruments, providing results ready for data review and QA. Assist in maintaining reagents and disposable supplies to ensure the lab operates efficiently. Perform raw materials, in process, finished products testing of solid dosage products. Qualifications: Life Sciences Bachelor’s degree or Science-based Associate’s degree (Chemistry preferred). 5-8 years of QC experience in a pharmaceutical or GMP environment. Experience with HPLC and/or GC quantitative analysis required Experience with Empower 3 software

RESPONSIBILITIES: Must be able to perform assigned sampling, physical, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemicals, physical and instrumental techniques (HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments) as per as per USP monograph / In-house / any other Compendial monographs. Must record data and results as specified in documentation procedures. Documents work clearly and perform tests accurately. Must comply with regulatory/in-house requirements (may include but not limited to safety, housekeeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity. Must prepare and review the analytical documents. Associate Chemist II will be responsible to prepare and/or Review Test Procedures, SOPs, and Protocols as assigned Responsible for maintaining independent verification testing progra