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Harmony Biosciences is recruiting for a Director, CMC Lead in our Plymouth Meeting, PA location. In this role you will be accountable for - and provide leadership to - interdisciplinary, matrix teams responsible for developing and executing product-specific integrated CMC strategies. The position is responsible for creating and formalizing the CMC strategy for multiple programs at various stages of lifecycle, to drive R&D / Commercial Franchise Team objectives and incorporate all CMC elements across drug substance, drug product, analytical, quality, regulatory CMC, and clinical/commercial supply. The CMC Lead will have a strong technical background and is expected to communicate and collaborate with the technical SMEs and lead the team in problem solving issues across the CMC functions.

Responsibilities include but are not limited to:

Lead cross-functional CMC teams for late-stage (Ph3 and launch) programs, while supporting programs in earlier (pre-clinical through Ph2) stages of development as necessary
Incorporate forward-thinking development plans, ensuring all necessary CMC activities will support registrational studies and commercial launch
Serve as the CMC \"asset owner\" with accountability to drive the creation and execution of Integrated 5-year CMC strategies and maintenance of 18-month rolling tactical project plans
Represent CMC on Franchise / Program Teams and actively collaborate with other functions (Clinical, Commercial, Regulatory, Clinical Pharmacology, Toxicology, etc.) to achieve the best development and business results for the company
Engage directly and extensively with operational and technical details across CMC functions, challenge technical SMEs, and lead effective problem-solving
Collaborate with Project Management, Quality, and Technical SMEs to manage key strategic vendor interactions for timelines, deliverables, and key milestones
Communicate and partner effectively with all functional areas within CMC (Technical Operations, Quality, Regulatory CMC), and other stakeholders (Pre-clinical Toxicology, Clinical Operations, Medical Affairs, etc.) to define and execute CMC strategies aligned with Franchise / Program Team Project Plans
Partner with CMC Project Managers to identify and escalate key issues and risks as well as resource allocation needs, as appropriate
Critically review relevant documents, including but not limited to all CMC regulatory submissions, briefing books, agency information requests, etc.
Lead or contribute to continuous improvement initiatives across the organization
Partner with the business development group to support or lead due diligence evaluations and activities associated with bringing in new assets in partnership with alliance management, as necessary

Qualifications:

Bachelor's degree required within scientifically relevant field (Chemical Engineering, Chemistry, etc.); Advanced degree MS / PhD / MBA is strongly preferred
8+ years experience of relevant pharmaceutical industry experience with a focus on CMC development and matrix management required
Track record of effective matrix leadership experience in the setting of program teams across the full product life cycle, e.g., CMC, Tech Ops line functions, Quality, Regulatory CMC, sub-teams or other cross-functional teams operating in a matrix environment ideally across an organization required
Broad understanding of CMC, supply chain, DS and DP development, or LCM development extending from IND to NDA and global launch & lifecycle including a solid understanding of global registration processes required
Technical expertise in a relevant pharmaceutical development discipline; experience with small molecules preferred
Demonstrated ability to lead, motivate, influence without authority a strategic direction; ability to effectively leverage and develop diverse perspectives and ideas from matrix teams and others
Excellent communication, negotiation, problem solving and decision-making abilities
Demonstrated ability to identify critical program risks and develop mitigation plans - strategic or tactical to mitigate risk, costs, and reputation of Harmony's business
Proficient in the use of Microsoft Office Suite required

Physical demands and work environment:

Travel (both domestic and international) is estimated to be 20% of the time for this position; Candidate must be able to maintain or obtain valid US Passport within 90 days of hire date. While performing the duties of this job, the noise level in the work environment can vary from relatively quiet (office) to moderate (laboratory/manufacturing). Hearing protection will be required at times.
Specific vision abilities required by this job include: close vision.
Manual dexterity required to use computers, tablets, and cell phone.
Continuous sitting for prolonged periods.

What can Harmony offer you?

Medical, Vision and Dental benefits the first of the month following start date
Generous paid time off and Company designated Holidays
Company paid Disability benefits and Life Insurance coverage
401(k) Retirement Savings Plan
Paid Parental leave
Employee Stock Purchase Plan (ESPP)
Company sponsored wellness programs
Professional development initiatives and continuous learning opportunities
A certified Great Place to Work for eight consecutive years based on our positive, values-based company culture

Want to see our latest job opportunities? Follow us on LinkedIn!

Harmony Biosciences is a pharmaceutical company headquartered in Plymouth Meeting, PA. The company was established in October 2017 with a vision to provide novel treatment options for people living with rare, neurological disorders who have unmet medical needs. For more information on Harmony Biosciences, visit www.harmonybiosciences.com

Harmony Biosciences is an Equal Opportunity, e-Verify Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

Recruitment agencies please note: Harmony Biosciences will only accept applications from agencies/business partners that have been invited to work on a specific role. Candidate Resumes/CV's submitted without permission or directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.

#LI-Hybrid

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The CMC Project Leader is accountable for the CMC project activities of mammalian projects of Sanofi’s R&D pipeline for pre-clinical and early clinical development from pre-candidate selection (PCS) to proof of concept (POC). The key accountability is to lead a cross-functional CMC team with members from R&D CMC including Mammalian DS platform, drug product & formulation platform, device development, Bioanalytics, Quality, Regulatory CMC, CMC dossiers, and Demand & Supply representatives in accordance to development phases.Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions. **About Sanofi:**We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.**Main responsibilities:*** The early-stage CMC Project Leader (CMC PL) is accountable for the CMC project activities of mammalian projects of Sanofi’s R&D Pharma pipeline for pre-clinical and early clinical development from pre-candidate selection (PCS) to proof of concept (POC).* For this mandate, he/she leads a cross-functional CMC team with functional members/sub-team leaders from R&D CMC including mammalian DS platform, drug product & formulation platform, Bioanalytics, device development, quality, regulatory CMC, CMC dossiers, and clinical supply chain as well as M&S representatives in accordance to development phases. He/she has an oversight in CMC and sub-teams of approximately 30-50 FTEs.* The CMC leader with his/her team in alignment with the CMC functions, creates a strategic and integrated CMC development plan based on global project objectives ensuring alignment with base case and accelerated plans and exploring opportunities for acceleration.* He/she represents the CMC team and functions as core member in the Global Project Team, contributes to overall project strategy and executes the appropriate actions within CMC to achieve project goals. Following the TPP, he/she defines the Quality Target Product Profile (QTPP)* He/she acts as overall product/process expert for the project and provides technical and scientific expertise on major project topics, drives and leads technical and scientific discussion and alignment within the CMC team and in R&D/M&S cross-functional governance meetings (Technical Review meetings, CMC Boards, RWG, DWG...).* He/she is responsible for quality of CMC contributions to pre-clinical and early clinical phase activities, and CMC elements for regulatory submissions and consultations. He/she assesses together with functions developability/manufacturability.* With the CMC team, he/she drives the evaluation of CMC risks and appropriately escalate to Senior Management (Cluster Head, Platform Head & Global Management as needed) and Global Project Team and proactively provides mitigation plans. He/she alerts decision makers and stakeholders to risks that can impact critical program timelines. In case of scientific/technical issues, he/she coordinates corrective measures across functions in cooperation with all relevant site and department heads.* He/she is responsible for implementation of CMC deliverables within budget considering external and internal costs. He/she leads and oversees planning of CMC project budget including communication and alignment with global project team and senior management.**About You**Education & Experience:PhD, MS, other university degrees in one of the areas of biopharmaceutical drug development (e.g., pharmaceutical chemistry, pharmacy, biology, biotechnology, biochemistry). Minimum of 10 years professional experience, ideally in CMC development, is required.Soft skills:* Leadership capabilities, strong team spirit and capacity to coordinate several activities and stakeholders.* Ideally experience in leading international and/or multi-cultural teams.* Good communication skills.* Ability to work in a matrix organization.* Experience in stakeholder management, ability to interact effectively with management and external bodies (e.g., auditors, health authorities, etc.), networking skills.* Influencing and negotiation skills to build solutions and partnership* Objectives and deliverables / results oriented. Capable to deliver under high pressure.* Take responsibility for decisions and accountable for results* Ability to challenge status quo and to propose alternatives.Technical skills:* Strong expertise in Biologics CMC area, with proven experience in at least 2 scientific areas, e.g., analytics, process development, regulatory CMC, manufacturing, etc.* Comprehensive scientific background in biotechnology and/or protein science.* Experience and understanding of current pharmaceutical environment including the economic and regulatory challenges.* Experience in working in cross-functional project team and in complex environment (e.g., activities across different sites).Languages: Fluent in English.**Why Choose Us*** Bring the miracles of science to life alongside a supportive, future-focused team.* Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.* Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.* Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.* Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.* Help improve the lives of millions of people globally by making drug development quicker and more effective.* Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.#GD-SA

#LI-SA

#vhd#LI-Hybrid# Pursue *progress*, discover *extraordinary*Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our

and check out our Diversity Equity and Inclusion actions at !*US and Puerto Rico Residents Only*Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive
#J-18808-Ljbffr
","**Job title**: *Project Leader CMC, Mammalian Projects Cluster** *Location: Framingham, MA***About the Job**Sanofi has an opening for a Project Lea...","Project Leader CMC, Mammalian Projects Cluster",[88],["B","3523541984"],"Work at Sanofi","/jobs/3523541984-project-leader-cmc-mammalian-projects-cluster","Framingham, MA, United States","/jobs?keyword=Sanofi","/jobs?location=Framingham%2C+MA%2C+United+States","/jobs?keyword=Project+Leader+CMC%2C+Mammalian+Projects+Cluster",{"_65":66,"_67":89,"_69":90,"_71":91,"_73":92},"Framingham","Framingham, MA, United States, 01704","MA","01704",["D",1777377600000],"Eacademy Sanofi","Job Title
Project Leader CMC, Mammalian Projects Cluster

Location
Framingham, MA

About the Job
Sanofi has an opening for a Project Leader role in our Chemistry Manufacturing & Control (CMC) organization. The CMC Project Leader is accountable for the CMC project activities of mammalian projects of Sanofi’s R&D pipeline for pre‑clinical and early clinical development from pre‑candidate selection (PCS) to proof of concept (POC). The key accountability is to lead a cross‑functional CMC team with members from R&D CMC including Mammalian DS platform, drug product & formulation platform, device development, Bioanalytics, Quality, Regulatory CMC, CMC dossiers, and Demand & Supply representatives in accordance to development phases.

Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI‑powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.

About Sanofi: We’re an R&D‑driven, AI‑powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main responsibilities

The early‑stage CMC Project Leader is accountable for the CMC project activities of mammalian projects of Sanofi’s R&D Pharma pipeline for pre‑clinical and early clinical development from PCS to POC.

Lead a cross‑functional CMC team with functional members/sub‑team leaders from R&D CMC including mammalian DS platform, drug product & formulation platform, Bioanalytics, device development, quality, regulatory CMC, CMC dossiers, and clinical supply chain as well as M&S representatives in accordance to development phases. Oversight of approximately 30‑50 FTEs.

With the CMC team, create a strategic and integrated CMC development plan based on global project objectives, ensuring alignment with base case and accelerated plans and exploring opportunities for acceleration.

Represent the CMC team as a core member in the Global Project Team, contribute to overall project strategy and execute the appropriate actions within CMC to achieve project goals. Following the TPP, define the Quality Target Product Profile (QTPP).

Act as overall product/process expert for the project, provide technical and scientific expertise on major project topics, drive and lead technical and scientific discussion and alignment within the CMC team and in R&D/M&S cross‑functional governance meetings (Technical Review meetings, CMC Boards, RWG, DWG…).

Responsible for quality of CMC contributions to pre‑clinical and early clinical phase activities, and CMC elements for regulatory submissions and consultations. Assess developability/manufacturability together with functions.

Drive evaluation of CMC risks with the team and appropriately escale to Senior Management and Global Project Team, provide mitigation plans, alert decision makers and stakeholders to risks that can impact critical program timelines. In case of scientific/technical issues, coordinate corrective measures across functions in cooperation with all relevant site and department heads.

Responsible for implementation of CMC deliverables within budget, lead and oversee planning of CMC project budget including communication and alignment with global project team and senior management.

About You
Education & Experience
PhD, MS, or other university degrees in biopharmaceutical drug development (e.g., pharmaceutical chemistry, pharmacy, biology, biotechnology, biochemistry). Minimum of 10 years professional experience, ideally in CMC development, is required.

Soft skills

Leadership capabilities, strong team spirit and capacity to coordinate several activities and stakeholders.

Experience leading international and/or multi‑cultural teams.

Good communication skills.

Ability to work in a matrix organization.

Experience in stakeholder management, ability to interact effectively with management and external bodies (e.g., auditors, health authorities), networking skills.

Influencing and negotiation skills to build solutions and partnership.

Objectives and deliverables / results oriented. Capable to deliver under high pressure.

Take responsibility for decisions and accountable for results.

Ability to challenge status quo and propose alternatives.

Technical skills

Strong expertise in Biologics CMC area, with proven experience in at least 2 scientific areas, e.g., analytics, process development, regulatory CMC, manufacturing.

Comprehensive scientific background in biotechnology and/or protein science.

Experience and understanding of current pharmaceutical environment including economic and regulatory challenges.

Experience working in cross‑functional project team and complex environments (e.g., activities across different sites).

Languages
Fluent in English.

Why Choose Us

Bring the miracles of science to life alongside a supportive, future‑focused team.

Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

Enjoy a thoughtful, well‑crafted rewards package that recognizes your contribution and amplifies your impact.

Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high‑quality healthcare, prevention and wellness programs and at least 14 weeks’ gender‑neutral parental leave.

Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real‑world needs.

Help improve the lives of millions of people globally by making drug development quicker and more effective.

Work at the forefront of drug discovery, harnessing cutting‑edge AI, data, and digital platforms to push the boundaries of science.

Equal Opportunity Employer
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, national origin, age, ancestry, nationality, marital, domestic partnership or civil union status, sex, gender, gender identity or expression, sexual orientation, disability, veteran or military status, domestic violence victim status, atypical cellular or blood trait, genetic information or any other characteristic protected by law.

#J-18808-Ljbffr
","Job Title
Project Leader CMC, Mammalian Projects Cluster

Location
Framingham, MA

About the Job
Sanofi has an opening ...",[103],["B","3522613088"],"Work at Eacademy Sanofi","23 hours ago","/jobs/3522613088-project-leader-cmc-mammalian-projects-cluster","/jobs?keyword=Eacademy+Sanofi",{"_65":66,"_67":89,"_69":90,"_71":91,"_73":92},["D",1777377600000],"Sanofi in Framingham, MA, is seeking a Real Time Series Product Owner to drive the development of innovative real-time data platforms. This role is key in connecting pharmaceutical manufacturing with digital innovation, managing product backlogs, and collaborating with R&D labs. The ideal candidate has a Bachelor's degree and 5+ years in product management with experience in data-intensive products. Sanofi offers a supportive environment focused on health and well-being, along with a competitive rewards package.
#J-18808-Ljbffr
","Sanofi in Framingham, MA, is seeking a Real Time Series Product Owner to drive the development of innovative real-time data platforms. This role is...","Real-Time Series Product Owner - AI-Driven Biopharma Data",[112],["B","3516236972"],"/jobs/3516236972-real-time-series-product-owner-ai-driven-biopharma-data","/jobs?keyword=Real-Time+Series+Product+Owner+-+AI-Driven+Biopharma+Data",{"_65":66,"_67":89,"_69":90,"_71":91,"_73":92},["D",1777377600000],"**Job Title:** *Real Time Series Product Owner** **Location:** *Framingham, MA***About the Job**Join the digital engine driving Sanofi’s transformation - where AI, automation, and bold experimentation power faster science and smarter decisions. Here, you’ll help build the first biopharma company powered by AI at scale.The Real-Time Series Product Owner is accountable for the vision, roadmap, and value delivery of real-time data acquisition and time‐series platforms in Sanofi R&D labs (Lucullus, MFCS, SynTQ...). The role sits within the Digital R&D organization, in the Lab Integration & Operations team, where you'll drive the development of innovative real supporting our CMC. This key role sits at the intersection of pharmaceutical manufacturing and digital innovation, leading the vision for real-time that transform how we leverage manufacturing data across Sanofi's global network.Join our Digital R&D organization Series Product Owner, where you'll drive the development of innovative real supporting our CMC an. This key role sits at the intersection of pharmaceutical manufacturing and digital innovation, leading the vision for real-time that transform how we leverage manufacturing data across Sanofi's global network.**About Sanofi**

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.**Main Responsibilities*** Define and communicate the vision, strategy, and roadmap for real-time time series data platforms supporting our CMC teams.* Drive product development through all stages from conception to launch, ensuring with Digital strategy* Manage the product backlog and prioritize features based on business value and CMC/M&S strategic priorities* Enable predictive analytics and advanced process control through time series data integration* Ensure solutions support GMP-compliant digital infrastructure requirements* Partner with M&S teams to enable data-driven process understandingStakeholder engagement* Act as primary point of contact between R&D labs (process development, analytical development, MSAT, QC where relevant) and technical teams for the covered products.* Facilitate requirement workshops with scientists, engineers, and lab operations to capture needs around experiment orchestration, PAT integration, method execution, and data visualization.* Communicate roadmap, release plans, and change impacts to stakeholders and governance forums in a clear and concise wayLab and system integration* Drive integration of Real Time Series platform

and related systems with lab instruments, data historians, LES/ELN, LIMS, MES, and enterprise data platforms.* Ensure data models, contextualization (batch, run, recipe, parameter metadata), and event/alert structures support downstream analytics, modeling, and reporting.* Collaborate with architecture and infrastructure teams on connectivity, performance, security, and scalability of time‐series data solutions (on‐prem and/or cloud).Compliance, quality, and operations* Ensure solutions and changes comply with GxP where applicable, data integrity expectations and cybersecurity standards.* Partner with QA, CSV, and validation teams to define validation strategies, risk assessments, and documentation for system and integration changes.* Define and track operational KPIs (system availability, data completeness, latency, incident volume), and support incident and problem management for the product family.Continuous improvement and value realization* Collect and analyze user feedback and usage data to refine backlog and maximize adoption and value of Real Time Series platform, Unicorn and associated services.* Champion best practices for digital lab workflows, real‐time monitoring, and data-driven decision making in partnership with scientific and operational stakeholders.* Identify opportunities to leverage advanced analytics, AI/ML, and digital twins on top of the time‐series data foundation.**About You**Required Qualifications* Bachelor's degree in Computer Science, Engineering, Information Systems, or related field* 5+ years of experience in product management with data-intensive products* Experience working with time series data, IoT platforms, or real-time analytics* Understanding of pharmaceutical CMC processes and GMP environments* Experience with agile product development methodologies* Ability to build business relationships and understand end-to-end digital product use and needsPreferred Qualifications* Knowledge of manufacturing execution systems (MES) and process* Familiarity with PI System/OSIsoft or similar industrial historians* Strong analytical skills with ability to interpret complex manufacturing data* Demonstrated ability to listen to stakeholders and end users, ensuring products are built to address their specific needs and use cases* Excellent communication and collaboration skills across technical and business teams* Experience developing products with Agile methodologies a must* Excellent stakeholder management and communication skills* Bring the miracles of science to life alongside a supportive, future-focused team.* Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.* Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.* Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.* Make your work count by supporting a company that brings life-changing treatments to millions — and is committed to doing right by patients, communities, and the planet.* Drive progress from within by helping simplify, scale, and modernize how a global biopharma business delivers smarter, faster, and more sustainably.* Support teams across science, medicine, and operations by building better systems, shaping bold strategies, and enabling innovation at speed.Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.#GD-SA

#LI-SA

#LI-Hybrid#vhd# Pursue *progress*, discover *extraordinary*Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our

and check out our Diversity Equity and Inclusion actions at !*US and Puerto Rico Residents Only*Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without
#J-18808-Ljbffr
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Newsday Media Group is a locally owned, independent media company grounded in journalistic excellence, integrity, and commitment to the communities it serves. With 19 Pulitzer Prizes and dozens of Emmy Awards, it's one of the most decorated news organizations in the country.

The company is in the middle of a significant transformation, expanding from its newspaper roots into a multimedia operation spanning digital, video, podcasts, live events, and data-driven civic engagement. NMG properties include the flagship Newsday and Newsday.com, NewsdayTV, the Newsday Live events series, and nextLI, a civic research and community forum platform funded by The Rauch Foundation.

A new 130,000-square-foot headquarters in Melville features a broadcast-quality TV studio and multimedia production space. Newsday Live produces a growing calendar of food and wine tastings, author talks, sports Q&As, concerts, and community events. Feed Me, the company's food and dining vertical, includes a web series, quarterly print magazine, and restaurant coverage. Brand 360, the in-house content studio, partners with advertisers across healthcare, education, energy, tourism, and retail.

Newsday's investigative unit has driven real-world change, from prompting schools to replace unsafe football helmets to contributing reporting that led to federal corruption convictions. Community programs include the Newsday Marching Band Festival, CheerFest, Scholar-Artist honors, and partnerships with local nonprofits focused on hunger, housing, youth education, and child welfare.

For people who care about local journalism, multimedia storytelling, and community impact, Newsday is doing the work at scale.

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