694 Seaport Global Holdings Llc jobs in New Jersey

High School diploma or equivalent
Valid driver's license, auto insurance, and reliable transportation
Ability to demonstrate high level communication skills
Strong problem-solving skills and ability to overcome objections and close sales
Self-motivated with a results-oriented mindset
Demonstrate accountability and enthusiasm for achieving financial goals
Ability to work independently with minimal supervision
Willigness to work outside 90% of the time for extended periods in any season, with potential exposure to inclement weather

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Hoboken - $18.50 hour - Fulltime Delivery Foot Courier delivering Amazon packages for Delivery One (the company)

Delivery One LLC

Hoboken, NJ 07030

$18.50/hr

OnsiteHealth InsurancePaid Time Off

MUST SPEAK PROFIECIENT ENGLISH
Eligible to work in the U.S [or Canada]
At least 18 years of age
Successfully pass a pre-employment drug test

SmartExplore AI is experimental.

New, Posted 17 hours ago

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Pressure Point Roofing LLC - Commercial Roofing Working Foreman

Pressure Point Roofing LLC

all cities, NJ

$35-$45/hr

OnsiteBilingual PreferredHealth InsurancePaid Time OffRetirement Benefit

Valid Driver's License
Minimum of 5 years of leadership experience specifically within the commercial roofing field
Proven proficiency in commercial roofing systems including TPO, PVC, and EPDM
Demonstrated ability to lead and hold crews accountable while maintaining high team morale
Absolute commitment to safety leadership and the consistent enforcement of OSHA standards
Physical ability to work in various weather conditions all year, work at heights, lift 70+lbs, and climb ladders

SmartExplore AI is experimental.

New, Posted 3 hours ago

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Utility Line Locator

UtiliQuest, LLC

Toms River, NJ 08753

OnsiteHealth InsurancePaid Time OffRetirement Benefit

To be 18 years of age or older
Authorization to work in the United States for this company
High School Diploma, GED equivalent, or relevant work experience
Valid State driver's license (cannot be Provisional), including an acceptable MVR record
**Routinely** : work alone in remote locations with arms above shoulder level, operate vehicle, squeeze, fine hand motion, bend, stoop, stand, walk, lift up to 55 pounds, use keyboard and mouse
**Occasionally** : use portable ladder, work in confined spaces and climb stairs

SmartExplore AI is experimental.

New, Posted 4 hours ago

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Delivery Driver

Pride Delivery Services Llc

Linden, NJ 07036

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Brand Manager, Neutrogena Global Makeup

Kenvue

Summit, NJ 07901

HybridPaid Time Off

Bachelor's degree in marketing, business administration, or a related field.
5-10 years of experience in marketing, with a focus on Beauty.
Makeup industry experience required.
Knowledge of the beauty industry is a must.
Ability to think creatively and strategically.
Strong analytical and problem-solving skills.
Experience in innovation and communications campaign development.
Excellent communication and collaboration abilities.
Ability to conduct and analyze customer and competitor research.
Experience in budget development for new product development and rollouts.

SmartExplore AI is experimental.

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Sr Manager Global Packaging Stewardship

Kenvue

Summit, NJ 07901

HybridPaid Time Off

Advanced degree in materials science or engineering, polymer science, chemistry, chemical engineering, or a related discipline.
Significant experience (typically 8–12+ years) in packaging stewardship, material design, sustainability or related roles within industry, consulting, or trade associations.
Strong understanding of packaging systems for consumer products, including plastics, paper, glass, metals, or emerging materials.
Demonstrated experience applying scientific and technical data in regulatory, policy, or advocacy contexts.
Proven ability to engage externally with industry groups, regulators, or technical stakeholders.
Excellent written and verbal communication skills, with the ability to translate complex topics for diverse audiences.

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Vice President, Global Regulatory Affairs, Team Lead, Strategy

Genmab

Plainsboro, NJ 08536

RemoteEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Advanced scientific degree required; PhD in a bioscience discipline (e.g., molecular biology, pharmacology, immunology, biochemistry, or related life sciences) or MD strongly preferred.
Minimum of 15+ years of progressive experience in Global Regulatory Affairs within the biotech or pharmaceutical industry, with at least 8–10 years in roles of increasing leadership responsibility.
Demonstrated track record of successful global regulatory submissions (IND/CTA, BLA/NDA/MAA, supplements, and life-cycle management) across major health authorities including FDA, EMA, PMDA, and Health Canada.
Extensive experience leading and interacting with health authorities, including successful execution of Type A/B/C meetings, Scientific Advice, End-of-Phase meetings, Pre-BLA/NDA meetings, and Advisory Committee preparations.
Significant experience in oncology, immunology, or other complex therapeutic areas (biologics, antibody-drug conjugates, bispecifics, or novel modalities preferred).
Deep expertise across the full product lifecycle — from early development through late-stage clinical, registration, launch, and post-marketing.
Proven experience leading regulatory strategy for partnered or co-developed programs, including negotiation with collaboration partners.
Demonstrated success building, leading, and scaling high-performing global regulatory teams across multiple geographies.
Experience representing Regulatory Affairs at the executive level Governance Committees as required.
Comprehensive knowledge of global regulatory frameworks, including FDA (21 CFR), EMA (EU CTR, EU MDR where applicable), ICH guidelines, and emerging markets regulations.
Expertise in expedited regulatory pathways (Breakthrough Therapy, Fast Track, Priority Review, Accelerated Approval, PRIME, Orphan Drug Designation).
Strong understanding of CMC regulatory requirements, nonclinical and clinical regulatory expectations, pharmacovigilance, labeling, advertising/promotion, and post-marketing commitments.
Working knowledge of companion diagnostics (CDx) co-development and combination product regulations, where relevant.
Familiarity with regulatory information management systems, eCTD publishing, and digital submission platforms.
Ability to interpret emerging regulatory guidance, policy, and legislation and translate implications into actionable strategy.
Strategic thinker with the ability to translate regulatory science into actionable commercial and development strategy.
Exceptional executive presence and communication skills; able to influence and align stakeholders at all levels, from technical teams to C-suite and Board.
Demonstrated ability to navigate complex, matrixed, global organizations and drive alignment across R&D;, Clinical, CMC, Commercial, Legal, and Medical Affairs.
Strong decision-making skills under uncertainty; comfortable balancing scientific rigor, regulatory risk, and business priorities.
Inspirational people leader with a strong track record of coaching, mentoring, and developing talent.
Cultural awareness and experience working across geographies, particularly across US, EU, and Asia-Pacific regions.
High integrity, resilience, and the ability to thrive in a fast-paced, science-driven biotech environment.
Collaborative mindset with a bias for action and continuous improvement.