NewProject Chemist/Data Validator Haley & Aldrich IncProject Chemist/Data ValidatorNew York City, NY$65,000–$85,000 / yearOur team of 1,000+ engineers and scientists across the United States draws inspiration from one mission: to work closely with clients as they navigate change to create safer, more robust places to live and work. In this role, you will play a vital part in supporting site assessment and remediation projects by performing comprehensive data validation on soil, water, and air environmental laboratory results.
NewSr Lab System Support Engineer@Rahway, NJ - onsite Diverse Lynx, LLCSr Lab System Support Engineer@Rahway, NJ - onsiteRahway, NJSr Lab System Support Engineer plays a key role in supporting laboratory operations by ensuring the smooth functioning of lab systems, analytical instruments, and data workflows. Lab System Lifecycle Management: Manage end to end lab system lifecycle including implementation validation maintenance and decommissioning.
Quality & Food Safety Supervisor Bunge LTDQuality & Food Safety SupervisorKearny, NJ$76,140–$85,657.50 / yearPlan, organize, and work under minimum supervision, provide analytical and troubleshooting assistance to the operations department, highlight deviations, collaborate and communicate effectively with various departments and managers, establish effective and open interpersonal relations, and perform related duties as required. Must be proactive and be able to demonstrate sound problem-solving skills, have experience with analytical instruments (GC, NIR, FTNIR, Spectrophotometer), Microbiological sampling and testing, and good knowledgeable of laboratory procedures and practices in edible oil crushing and refining or manufacturing environment.
NewSenior Scientist, Regulatory CMC ImmunityBioSenior Scientist, Regulatory CMCSummit, NJImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. This position will support the development of submission strategies for CMC modules and updates, including life cycle management; and generation of submission-ready content for the Quality/CMC sections of all clinical trial and marketing authorization applications for ImmunityBio, Inc.
NewPrincipal Scientist, Regulatory CMC ImmunityBioPrincipal Scientist, Regulatory CMCSummit, NJImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. Key responsibilities will include contributing to the development of submission strategies for CMC modules and updates, including life cycle management; and generation of submission-ready content for the Quality/CMC sections of all clinical trial and marketing authorization applications for ImmunityBio, Inc.
Annual Product Quality Review Program Lead Tris PharmaAnnual Product Quality Review Program LeadMonmouth Junction, NJ$100,000–$145,000 / yearMinimum education and years of relevant work experience: Bachelors degree in Chemical Engineering, Pharmaceutical Sciences, Chemistry, or a related scientific discipline and minimum 5 years in quality systems, process validation, product quality review or quality engineering in the pharmaceutical or biotechnology industry in positions of increasing technical responsibility OR combination of education and related quality systems, process validation, product quality review or quality engineering in the pharmaceutical or biotechnology industry in positions of increasing technical responsibility. Analyzes and interprets large datasets from Manufacturing, Packaging, Laboratory departments, complaints, deviations, Corrective Action Preventive Action (CAPAs), change controls and stability programs to identify statistically significant trends, process shifts and emerging quality risks including, but not limited to: analyzing Deviation and Rejection Profiles, trending manufacturing deviations, batch failures, yield losses and Out-of-Specification (OOS) laboratory findings (i.e., dissolution, uniformity, particle size), etc.
Director Business Development - Mobile AC - Remote Solstice Advanced Materials IncDirector Business Development - Mobile AC - RemoteMorris Plains, NJRemote$226,930–$283,369 / yearAlign with Sales Leadership at the executive level, provide strategic direction for target account planning, lead a rigorous business development MOS, and hold accountability for the prioritization of business opportunities and cross-functional resource allocation. You will champion innovation and growth in new segments at the executive level, build and steward high-impact strategic customer relationships, and lead the identification and evaluation of mergers, acquisitions, joint ventures, and other strategic alliances.
SAP Logistics and Operations Lead Quidelortho CorpSAP Logistics and Operations LeadRaritan, NJRemoteAs the organization is embarking on extending functional use of these SAP Modules and launching other cutting-edge tools, we are looking for a SAP Logistics and Operations Lead for design, implementation and ongoing support of core SAP functionality and best of breed applications for Logistics, Plant Maintenance, Quality Management and Manufacturing execution. QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine.
NewSAP Functional Lead (Manufacturing, Plant Maintenance And Quality Management) QuidelOrtho CorporationSAP Functional Lead (Manufacturing, Plant Maintenance And Quality Management)Raritan, NJRemoteAs the organization is embarking on extending functional use of these SAP Modules and launching other cutting-edge tools, we are looking for a SAP Functional Lead for design, implementation and ongoing support of core SAP functionality and best of breed applications for Logistics, Plant Maintenance, Quality Management and Manufacturing execution. QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine.
Senior Developer D&A - Beverages DoehlerSenior Developer D&A - BeveragesPrinceton, NJ$115,000–$125,000 / yearAdditionally, the role involves maintaining detailed project documentation, supporting product trials and scale-ups, troubleshooting formulation challenges, and driving continuous improvement throughout the product development process. The D&A Developer is responsible for managing and executing development projects from concept through completion, ensuring they are delivered efficiently, accurately, and in alignment with quality and business objectives.
Manufacturing Technician Integrated Resources, IncManufacturing TechnicianPlainsboro Township, New JerseyContractorManufacturing TechnicianJob DescriptionInterface with area leadership and other support groups to execute cleaning processesProvide immediate feedback to area leadership on process deficiencies or delaysDemonstrate respect, encouragement and teamwork to peers to complete daily tasksMaintain prompt time management around start/stop and breaks with a focus on timely task completionMust pass and maintain gowning qualification required to access the manufacturing controlled areasMust perform all related cleaning processes per current proceduresPerform daily equipment cleaning, set up, and disassemblyPerform visual equipment cleaning inspections and must be able to identify "cleaned" and "used"Must be able to understand and follow cGMP; QSR, USP and ISOPerform additional production support tasks as assigned including cross-trainingReconcile all materials into and out of the manufacturing controlled areasSupport department and plant Safety goals by continuously demonstrating safe behaviorAbility to work flexible shifts, and flexible days within the week to meet requirementsPaperworkDocument entries clearly and legibly per good documentation practicesPerform in-process data entry reviews and support resolution to deficienciesPerform math operations to determine formulation requirements and reconciliationsQualificationHigh School diploma or equivalent. Degree in related science a plus.1 to 2 years of cleanroom experience in the Medical Device or Pharmaceutical/Biotech industryBasic computer skills for email and data entryMust be able to lift 50-60lbsMust read, write and speak in English, and communicate clearly and concisely.
LCMS Sales Specialist II (Liquid Chromatography Mass Spectrometry) Shimadzu Scientific Instruments, Inc.LCMS Sales Specialist II (Liquid Chromatography Mass Spectrometry)Somerset, NJ$100,000–$105,500 / yearPart timeIn this role, you will act as a consultative sales expert, taking full ownership of a defined territory (Eastern Pennsylvania, New Jersey, New York City, Long Island) and associated product lines while strategically developing the territory for sustainable year-over-year growth. Shimadzu Scientific Instruments is seeking a LCMS Sales Specialist II to promote and grow sales of Shimadzu’s premier LCMS portfolio, including LCMS Single Quad, LCMS-QQQ, Q-TOF, MALDI, CLAM, Applications Specific Accessory devices and Application Specific Software’s.
Sr. Regulatory Affairs Specialist Integrated Resources, IncSr. Regulatory Affairs SpecialistEdison, New JerseyFull timeRegulatory Affairs SpecialistA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. This is a Direct Hire role with the clientJob DescriptionJOB SUMMARYThis person will be a Regulatory liaison between product development and the regulatory agencies.
Chemist Integrated Resources, IncChemistElizabeth, New JerseyFull timeJob DescriptionBachelor's degree in Chemistry or related science from an accredited college or university; and a minimum of 1-3 years of related laboratory work experience in a pharmaceutical environment; or an equivalent combination of training and experience. Physical Requirements and Working Conditions: Incumbents in this class are subject to extended periods of sitting, standing, walking, lifting materials weighing up to 50 pounds, vision to monitor and moderate to loud noise levels.
Scientist I, DMPK / ADME WuXi AppTecScientist I, DMPK / ADMECranbury, New JerseyOverview: Associate Scientist I is responsible to conduct routine in vitro ADME assays in compliance with applicable methods, including but not limited to weighing the chemical, preparing the solutions, performing assays, and generating the data reports. Learn and enhance technical knowledge of in vitro ADME assays, such as stability, CYP inhibition/induction and transporter, etc, as well as technical knowledge of DMPK including ADME, PK, Metabolism, and bioanalysis.
Pool Service Valet INFINITE BLU POOL SERVICES LLCPool Service ValetKenilworth, NJ$20–$24 / hourFull timeThis role involves performing routine pool cleaning, water chemistry balancing, equipment inspections, and customer service support. We are seeking a reliable and detail-oriented Pool Cleaner / Valet Technician to join our team for the seasonal pool service period.
Quality Control Laboratory Technician Aquinas ConsultingQuality Control Laboratory TechnicianBranchburg, NJStrong organizational and communication skills with the ability to follow SOPs, interpret routine technical data, multitask in a fast-paced environment, and experience with LIMS or SAP is a plus. Qualifications: Associate's degree in Chemistry, Physics, or a related scientific discipline with two or more years of laboratory experience, or a Bachelor's degree with demonstrated hands-on laboratory experience.
Urgent Hiring Medical Laboratory Scientist In Clifton NJ 07012 eTeam Inc.Urgent Hiring Medical Laboratory Scientist In Clifton NJ 07012Clifton, NJ$30–$40 / hourFollow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result; 2. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens; 3. Analyze specimens using approved testing procedures (see department SOPs). Identify problems that may adversely affect test performance or reporting of test results, correct the problems encountered or immediately notify the senior technologist or supervisor.
Scientist II or III - Automation Scientist - FSP ParexelScientist II or III - Automation Scientist - FSPNew JerseyFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. These platforms include high-throughput systems from Tecan and Unchained Labs, as well as medium-throughput platforms from Technobis, Mettler Toledo Quantos, Trajan Chronect, and similar systems.
Vice President, Business Development - Life Sciences Gerson Lehrman Group IncVice President, Business Development - Life SciencesNew York, NY$117,000–$120,000 / yearThe role is responsible for originating and developing strategic partnerships across top 30 global pharmaceutical, biotech, medtech and diagnostics companies, as well as high-growth innovators, and for materially increasing GLG's share of wallet within these accounts. We connect global decision-makers-from hedge fund managers and private equity partners to strategy leaders at Fortune 500s-with the specific, authoritative voices required to answer their most critical questions.