Biotechnology jobs in livingston, nj

Principal Maximo Integration Architect / M&A Cutover Lead

Ridgefield, New Jersey

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6d ago

Job Title: Principal Maximo Integration Architect / M&A Cutover Lead Location: Ridgefield, New Jersey (Onsite) - 4-5 days a week Project: M&A Maximo Migration Position Summary We are seeking a highly experienced Principal Maximo Integration Architect / M&A Cutover Lead to lead the technical architecture, integration strategy, and cutover execution for an enterprise IBM Maximo migration supporting a large-scale Mergers & Acquisitions (M&A) separation initiative. The ideal candidate will possess

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Contract, Third Party

Depends on Experience

Product Designer

New York, New York

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Today

Founding UX/UI Designer - Williamsburg, Brooklyn (Hybrid) Our client is a well-funded, early-stage biotechnology startup building artificial intelligence-driven drug development platforms. Backed by a premier accelerator and founded by a leading university research team, they train foundation models on human cellular and molecular data. Their technology translates complex biological patterns into actionable decision systems for drug response, toxicity, and diagnostics. They are seeking a UX/UI D

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Contract

USD 60.00 - 75.00 per hour

Field Service Engineer - NYC

New York, New York

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Today

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Beckman Coulter Life Sciences, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - inn

Full-time

USD 31.00 - 38.00 per hour

CSV Lead

Hybrid in Raritan, New Jersey

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Today

Job Title: CSV Lead Location - Raritan, NJ (Hybrid) W2/C2C Mandatory Skills - LIMS Lab Vantage & CSV Job Summary: Experience in the Pharmaceutical, biotechnology with LIMS Labvantage related System Development Lifecyle in Computer System Validation Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation. Knowledge of FDA guidances and industry standards (i.e., GAMP) Experience in writing and executing documentation for all as

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Contract, Third Party

55 - 60

Automation Engineer

New York, New York

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Today

About Us: The people of Memorial Sloan Kettering Cancer Center (MSK) are united by a singular mission: ending cancer for life. Our specialized care teams provide personalized, compassionate, expert care to patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, di

Full-time

USD 83,800.00 - 134,000.00 per year

CSV Consultant(Computer System Validation ? GenAI, Agentic , SAP

Raritan, New Jersey

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Today

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Contract

USD45.0/HOURLY - USD52.0/HOURLY

Field Service Engineer I/II

New Brunswick, New Jersey

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Today

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

Full-time

USD 27.00 per hour

Automation Engineering Technician Sr.

Livingston, New Jersey

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Today

Job Description Scope: The Genomics Automation Specialist serves as the technical owner for assigned laboratory automation systems at the Livingston site. This position is responsible for ensuring reliable, compliant, and efficient operation of automated laboratory platforms through preventive maintenance, troubleshooting, validation support, lifecycle management, and continuous improvement. The role partners closely with Automation Engineering while progressively assuming ownership of assigned

Full-time

Claims Consultant -Life Sciences or Cyber/Technology E&O (Hybrid)

New York, New York

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Today

Our employees are at the heart of what we do: helping people, businesses and society prosper in good times and be resilient in bad times. When you join our team, you are bringing this purpose to life alongside a passionate community. Feel empowered to learn and grow while being valued for who you are. At Intact, we commit to supporting you in reaching your goals with tools, opportunities, and flexibility. It's our promise to you. Who we are At Intact Insurance Specialty Solutions, we are exper

Full-time

USD 123,000.00 - 163,000.00 per year

Clinical Domain Consultant : NJ/MD/CA

Jersey City, New Jersey

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Today

Title: Clinical Domain ConsultantLocation: NJ/MD/CA JD: Role OverviewWe are seeking an experienced Clinical Domain Consultant with strong expertise in the Pharmaceutical and Life Sciences clinical domain. The ideal candidate will have hands-on experience across clinical development and clinical trial operations and will serve as a bridge between business stakeholders, clinical teams, data teams, and technology teams. The consultant will help translate complex clinical business requirements into

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Contract, Third Party

Depends on Experience

Alliance Manager - Personalized Healthcare Solutions

Remote or Hybrid in Tucson, Arizona

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Today

Greetings from IT Engagements IT Engagements is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. We have an immediate opening for the below position with one of our premium clients. Job Summary Required: 3+ years** of Alliance Management experience in pharmaceuticals, biotechnology, or diagnostics Bachelor's degree in Life Sciences, Business, or a related field Preferred: Hands-on experience with Salesforce and Conga CA-AM or CSAP certif

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Contract

$$73

IBM Maximo Architect || Ridgefield, NJ

Ridgefield, New Jersey

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5d ago

Principal Maximo Integration Architect / M&A Cutover Lead Principal Maximo Integration Location: Ridgefield, New Jersey (Onsite) - 4-5 days a week Description Position Summary We are seeking a highly experienced Principal Maximo Integration Architect / M&A Cutover Lead to lead the technical architecture, integration strategy, and cutover execution for an enterprise IBM Maximo migration supporting a large-scale Mergers & Acquisitions (M&A) separation initiative. The ideal candidate will possess d

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Contract, Third Party

Depends on Experience

Senior Director, Information Technology (BioPharma Industry)

Morristown, New Jersey

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Today

Description The Senior Director, Information Technology will lead enterprise technology strategy, infrastructure, cybersecurity, GxP validation, SOX compliance, and the business application roadmap for a growing late-stage clinical biopharmaceutical organization transitioning toward commercialization. This role will architect scalable technology capabilities, establish practical governance, and align IT with business objectives. The leader will manage a small internal IT team, oversee managed s

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Full-time

USD 210,000.00 - 255,000.00 per year

IT Project Manager with GxP

Remote

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4d ago

Title: IT Project Manager with GxP Location: Boston MA (1x Month) Duration: 6 Months Visa: No H1b Need an IT/Infrastructure PM with recent Pharma and GXP experience. Must have experience working with MSPs or Vendors Description: The Project Manager will be responsible for the end-to-end project lifecycle of multiple simultaneous IT projects in a GxP regulated environment. The PM will engage in new and in-flight projects to ensure project resources are aligned to deliver on schedule and within

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Full-time

70 - 75

Regulatory Specialist

Remote

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3d ago

Job Title:Regulatory Specialist Location:Rosemont, IL - Remote Duration: Long Term Contract Key Responsibilities: Provide strategic input and technical guidance on regulatory requirements to R&D project teams. Develop and implement regulatory strategies to facilitate the progress of US and Global programs and initiatives for the company. Evaluate regulations, establish framework, and design and implement science-based registration strategies for company products to ensure rapid, high-quality s

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Contract

Depends on Experience

Third Party Risk Manager

New York, New York

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2d ago

Your Journey at Crowe Starts Here: At Crowe, you can build a meaningful and rewarding career. With real flexibility to balance work with life moments, you're trusted to deliver results and make an impact. We embrace you for who you are, care for your well-being, and nurture your career. Everyone has equitable access to opportunities for career growth and leadership. Over our 80-year history, delivering excellent service through innovation has been a core part of our DNA across our audit, tax, an

Full-time

USD 59,800.00 - 114,500.00 per year

Staff Automation Engineer

Raritan, New Jersey

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Today

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m

Full-time

USD 94,000.00 - 144,500.00 per year

Engineer Pharma Validation

Remote

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Today

Job Summary Responsible for the validation of facility utilities, equipment processes and cleaning for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210, 21 CFR 820, and other applicable regulatory requirements. Assist in authoring and executing protocols to demonstrate that manufacturing and cleaning processes are executed with consistent quality and results within a controlled environment. Responsible for managing and or performing reval

Full-time

USD 73,000.00 - 110,000.00 per year

AI Data Engineer - Scientific Data Platforms (Remote)

Remote or South San Francisco, California

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Today

Pay Rate Low: 35 | Pay Rate High: 40 Our client is a leading global biotechnology and pharmaceutical organization driven by a mission to innovate, continuously advance science, and ensure everyone has access to the healthcare they need. Title: AI Data Engineer - Scientific Data Platforms Location: Remote, Must work PST Pay rate: $35-38/hr (Depends on experience level) Schedule: Full-time (40 hours/week) Duration: 1-year contract, (Plus benefits) Position Overview This role addresses a crit

Full-time

USD 35.00 - 38.00 per hour

eTMF Specialist, Pharma, BiAnnual Review Project

Remote or Almont, Colorado

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Yesterday

Description: Remote Our client is seeking an eTMF Specialist to support a biannual review of Phase Trial Master Files. The specialist will ensure TMFs are complete, accurate, compliant, and inspection-ready through comprehensive quality review and collaboration with internal and external stakeholders. Due to client requirements, applicants must be willing and able to work on a w2 basis. For our w2 consultants, we offer a great benefits package that includes Medical, Dental, and Vision benefi

Contract

Biotechnology jobs in Livingston, NJ, USA