UNKNOWN

FEED

During this 12-week program, interns will gain practical exposure to clinical trials, data management processes, technology platforms, global regulations, and cross-functional drug development while contributing to projects that support the delivery of medicines to patients. Purpose: The Data Management and Central Monitoring (DM CM) Summer Internship provides undergraduate students with hands-on experience supporting clinical data management and data acquisition activities within Global Development.

HOUR

Caring for the world, one person at a time... inspires and unites the people of Johnson&nbsp;&amp;&nbsp;Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson&nbsp;&amp;&nbsp;Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.

Our Family of Companies comprises:

 The world’s sixth-largest consumer health company. 
 The world’s most comprehensive medical devices business. 
 The world’s sixth-largest biologics company. 
 And the world’s fifth-largest pharmaceuticals company. 


We have more than 265 operating companies in more than 60 countries employing approximately 126,500 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.

Johnson & Johnson

Idar Summer Intern (DM CM)

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Qualifications/Skills Entrepreneurial personality, energetic and accountable in accomplishing the objectives of the business Strong communication skills Problem Solver High Performer able to manage and negotiate multi-million dollar contracts Ability to inspire customer confidence, promote and develop strong client to business relationships and become the provider of choice for existing and new clients. At Cambrex, we strive to build a culture where all colleagues have the opportunity to: engage in work that matters to our customers and the patients they serve learn new skills and enjoy new experiences in an engaging and safe environment strengthen connections with coworkers and the community We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company.

Cambrex is an innovative life sciences company with a refreshingly human approach. Driven by passion, our pharmaceutical products, expertise and technologies accelerate our customers’ small molecule therapeutics into markets across the world.

With over 35 years of active pharmaceutical ingredient (API) development and manufacturing expertise, a growing team of more than 1,200 experts and a strong presence in the USA and Europe, we are tried and trusted across branded and generic API markets.

Cambrex Corp

Director, Account Management

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This role owns a broad portfolio across the revenue lifecycle, including order and data capture, eligibility and coverage, prior authorization, clinical documentation, billing and claim readiness, patient financial experience and self-pay, vendor integrations, denials, and outcome measurement. With over 20 years of expertise in diagnosing rare disorders and diseases, and pioneering work in the identification of new disease-causing genes, our commitment to genetic disease detection, discovery, and diagnosis is based on sound science and is focused on enhancing patient care.

YEAR

GeneDX LLC

Product Lead, Revenue Cycle Management

Performs testing of raw materials, packaging components, IP, FP and/or ST samples including dissolution, assay, related compounds analysis, content/blend uniformity, particle size distribution by Malvern/Sieve, bulk and Tap density, cleaning validation and other tests according to the analytical methods, United States Pharmacopeia (USP) procedures in a regulated laboratory environment. Operates general analytical instruments during raw material, IP and FP testing such as High Pressure Liquid Chromatography (HPLC), UltraPerformance Liquid Chromatography (UPLC), Gas Chromatography (GC), Ultra Violet visible spectroscopy (UV/Vis), automatic titration, Infra-Red Spectroscopy (IR), Malvern Mastersizer, Thin Layer Chromatography (TLC) and dissolution apparatus (Distek).

Tris Pharma

QA R&D Chemist I

This role is responsible for applying formulation science, ingredient knowledge, consumer insights, and competitive intelligence to support innovation across categories such as hand sanitizers, skin care, body care, deodorants, mists, and other personal care and OTC products. The actual base pay offered to the successful candidate will be based on multiple factors, including, but not limited to, job-related knowledge/skills, experience, business needs, geographical location, and internal pay parity.

Church & Dwight Co. Inc. (CHD), a $3.5 billion company, was founded in 1846 and is headquartered in Ewing, New Jersey. We are one of the fastest growing Consumer Packaged Goods companies that has outpaced the Standard & Poor's by more than two times over the last 10 years.

Church & Dwight is a leader in the Household Consumer Products and Personal Care industry, with such brands as ARM & HAMMER, Trojan, First Response, Nair, Spinbrush, Oxi Clean, Orajel, VitaFusion and Xtra.

The Company’s business is divided into three primary segments, Consumer Domestic, Consumer International and Specialty Products.

The Consumer Domestic segment includes our eight power brands, ARM & HAMMER, Trojan, First Response, Nair, Spinbrush, Oxi Clean, Orajel, VitaFusion, and XTRA and other household and personal care products.

Church & Dwight

Research Chemist

The Senior Research Chemist in upstream innovation will play a critical role in assessing new technologies and areas for innovation to advance the global innovation pipeline of personal care businesses such as TheraBreath, HERO, and Batiste, impacting more than 1 billion dollars in company sales. This position requires a strong background in oral care, consumer goods chemistry, extensive knowledge of good laboratory practices, experience translating consumer insight into executable innovation, and an understanding of how to take products from idea to the commercial market.

Church & Dwight Co Inc

Senior Research Chemist

Working at Intertek means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustainability to life. Intertek, a leading provider of quality and safety solutions to many of the world's top-recognized brands and companies, is actively seeking a Chemical Technician III to join our Chemicals & Pharmaceuticals team in Whitehouse, New Jersey.

Intertek Group Plc

Chemical Technician (Inorganic Spectroscopy)

The Senior Software Developer will develop modular Python-based analytical applications and supporting software, contribute to differential privacy and disclosure-avoidance tools, build evaluation applications, support production analytical pipelines and automated output generation, develop dashboards and technical tools, ensure reproducibility and scalability, and support documentation, testing, training, and Government knowledge transfer. E-Logic, Inc. is seeking a Senior Software Developer to support the development, testing, implementation, validation, and optimization of software applications and analytical tools supporting the IRS RAAS Statistics of Income (SOI) Division's production of differentially private Qualified Opportunity Zone statistics.

E Logic

Senior Software Developer

The Hire Talent

To conform to U.S. Government export regulations applicable to that information, applicant must either be (A) a U.S. person, defined as a (i) U.S. citizen or national, (ii) U.S. lawful permanent resident (green card holder), (iii) refugee under 8 U.S.C. § 1157, or (iv) asylee under 8 U.S.C. § 1158, (B) eligible to access the export controlled information without a required export authorization, or (C) eligible and reasonably likely to obtain the required export authorization from the applicable U.S. government agency. Trusted by leading AI labs, startups, and global enterprises, CoreWeave combines superior infrastructure performance with deep technical expertise to accelerate breakthroughs and turn compute into capability.

Core Weave

Staff Data Engineer - Data Engineering

FULL_TIME

The role will lead phase-appropriate development, scale-up, technology transfer, manufacturing, control strategy, validation readiness, and lifecycle activities for peptide drug substance programs, while serving as a key technical interface with external CDMOs and internal Quality, Regulatory, Drug Product, Clinical Supply, and program teams. The Company's lead candidate, pemvidutide, is a unique dual-action therapy targeting both glucagon and GLP-1 receptors in a balanced 1:1 ratio in development for the treatment of metabolic dysfunction-associated steatohepatitis (MASH), alcohol use disorder (AUD), and alcohol-associated liver disease (ALD).

Altimmune

Senior Director, Drug Substance Development

Talent Acquisition

OTHER

Train end users, upskill internal teams, and lead structured knowledge transfer sessions to enable independent system support. Employees hired into this position are eligible for the following benefits, subject to the applicable plan terms and eligibility requirements: Health Insurance: Medical, dental, and vision insurance options are available through a third-party provider.

Intellectt INC

LabVantage LIMS/ELN Consultant

Ceipal

Required Skills: Preferred Skills: Analytical Reasoning, Budgeting, Business Savvy, Consulting, Econometric Models, Financial Analysis, Financial Competence, Financial Forecasting, Financial Modeling, Financial Planning, Financial Reports, Financial Risk Management (FRM), Industry Analysis, Internal Controls, Organizing, Project Management, Technical Credibility. All Job Posting Locations: Palm Beach Gardens, Florida, United States of America, Raritan, New Jersey, United States of America, Raynham, Massachusetts, United States of America, Warsaw, Indiana, United States of America, West Chester, Pennsylvania, United States of America.

Senior Manager, Data Science

Working within an agile delivery model, you will partner closely with business stakeholders, Data Engineers, Data Scientists, AI Engineers, Architects and Technology experts to design, test and deliver solutions that are practical, scalable and aligned to measurable business outcomes. Work as an active member of cross-functional agile delivery teams, partnering closely with Data Engineers, AI Engineers, Data Scientists, Architects, Technology experts and business product owners.

Axis Capital Holdings LTD

Insights & Analytics Lead - North America

The Executive Director, Quality Control will be responsible for all aspects of quality control, from drug development through commercialization, including the manufacture of clinical products, conducting clinical trials, oversight of GCP and GLP CROs, and the manufacture/distribution of commercial products globally. This role will also be responsible for leading science-driven, phase appropriate analytical development to support clinical programs to commercial registration and post-approval improvements both internally and at third party contractors.

Revance

Executive Director, Quality Control

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You'll also: Partner with cross-functional stakeholders, including Therapeutic Area teams, Clinical Pharmacology, Clinical Operations, Nonclinical Safety, Regulatory Affairs, Biometrics, and external collaborators, to develop and execute integrated Translational Bioanalytical and Biomarker strategies that support clinical development programs. Who You Are: You have a PhD in Analytical Chemistry, Pharmacokinetics, Pharmacology, Pharmaceutics, Bioanalytical Sciences, or a related discipline, along with a minimum of 10 years of progressive experience in the biopharmaceutical or pharmaceutical industry, with substantial experience supporting translational sciences, bioanalysis, biomarkers, and clinical development.

Insmed Inc

Director, Translational Bioanalytical Sciences

This role requires close collaboration with regional sales teams, application specialists, marketing, regulatory affairs, and business units to identify growth opportunities and develop strategic commercial plans that accelerate Waters leadership in PFAS analysis. The role will focus on positioning Waters PFAS analytical solutions, workflows, applications, consumables, informatics, and services to enable laboratories to expand testing capacity, improve productivity, and respond to evolving regulatory requirements.

Waters Corp

Business Development Manager PFAS

To conform to U.S. Government export regulations applicable to that information, applicant must either be (A) a U.S. person, defined as a (i) U.S. citizen or national, (ii) U.S. lawful permanent resident (green card holder), (iii) refugee under 8 U.S.C. § 1157, or (iv) asylee under 8 U.S.C. § 1158, (B) eligible to access the export controlled information without a required export authorization, or (C) eligible and reasonably likely to obtain the required export authorization from the applicable U.S. government agency. You need to be technically fluent enough for the real architecture conversations: relational data modeling and query performance at scale, object storage, an analytical search index maintained alongside a transactional system of record, permission models, and the lifecycle of data customers cannot afford to lose.

CoreWeave Inc

Engineering Manager, Artifacts & Registry - W&B

Minimum of 10 years of progressive hands-on experience in medical device product development under FDA Quality System Regulation (21 CFR Part 820) and ISO 13485, with a demonstrated track record of successfully advancing complex electromechanical or electro-fluidic devices from concept through verification, validation, and commercialization. Effectively synthesize, condense, and communicate complex technical data, experimental results, trade-off analyses, and risk assessments through clear presentations, design reviews, and written reports for cross-functional audiences including R&D, Quality, Regulatory, Manufacturing, and senior leadership.

Integra LifeSciences Holdings Corp

Sr Principal Engineer, Product Development

As the Subject Matter Expert and Issue Manager for key contaminants, including mycotoxins, heavy metals, mineral oils, 3-MCPDE/GE, plasticizers, pesticides, and PFAS, you will lead risk assessments, investigate emerging issues, and provide expert guidance across the organization. 5-8 years of experience in the food industry within Quality, Food Safety, Analytical Chemistry, or Toxicology, with expertise in contaminants such as mycotoxins, heavy metals, process contaminants, mineral oils, pesticides, PFAS, and packaging migrants.

Nestle SA

Senior Chemical Contaminant Risk Specialist (Hybrid)

Follow SOPs to manage our chemical compound collection for both catalog chemicals and client compounds, including registration of compound, weighing of compounds, preparing data sheets, labels and other documents. Genesis Drug Discovery and Development (GD3 or Company), a member of the Genesis Global Group, is a fully integrated CRO providing services to support drug discovery programs of our clients from target discovery through GLP tox studies.

Analytical Scientist Jobs in New Jersey

Idar Summer Intern (DM CM) Johnson & Johnson

Director, Account Management Cambrex Corp

Product Lead, Revenue Cycle Management GeneDX LLC

QA R&D Chemist I Tris Pharma

Research Chemist Church & Dwight

Senior Research Chemist Church & Dwight Co Inc

Chemical Technician (Inorganic Spectroscopy) Intertek Group Plc

Senior Software Developer E Logic

Staff Data Engineer - Data Engineering Core Weave

Senior Director, Drug Substance Development Altimmune

LabVantage LIMS/ELN Consultant Intellectt INC

Senior Manager, Data Science Johnson & Johnson

Insights & Analytics Lead - North America Axis Capital Holdings LTD

Executive Director, Quality Control Revance

Director, Translational Bioanalytical Sciences Insmed Inc

Business Development Manager PFAS Waters Corp

Engineering Manager, Artifacts & Registry - W&B CoreWeave Inc

Sr Principal Engineer, Product Development Integra LifeSciences Holdings Corp

Senior Chemical Contaminant Risk Specialist (Hybrid) Nestle SA

Research Assistant Comparative Biosciences Inc

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