3359 Ehs Safety Manager Director jobs in East Brunswick,NJ

New, Posted 3 hours ago

EHS Specialist

Amazon

Staten Island, NY 10314

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Maintenance Supervisor

Adecco

New Brunswick, NJ 08901

$105,000/yr

~ 15 min OnsiteHealth InsuranceRetirement Benefit

Associates degree in electro-technology or similar, military technical training and/or trade/vocational schooling
Experience with PLC's
5+ years in a high-volume or high-speed environment
2+ years supervising or leading maintenance staff
Understanding of LEAN 5S, GMP, and OHSA standards

SmartExplore AI is experimental.

New, Posted 1 hour ago

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Remote Customer Service

Hire Standard Staffing

East Brunswick, NJ

$120,000/yr

RemoteHealth Insurance

Must be a U.S. or Canadian citizen

SmartExplore AI is experimental.

New, Posted 3 hours ago

Associate Director, Continuous Improvement (Onsite)

Merck & Company

Rahway, NJ 07065

New, Posted 3 hours ago

Global Facilities Director

CBRE Group

New York, NY 10025

New, Posted 3 hours ago

Strategy and Operations, Associate Director

Bristol Myers Squibb

Princeton, NJ 08540

New, Posted 11 hours ago

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Assistant Director

The Learning Experience

East Brunswick, NJ 08816

$50,000/yr

OnsiteFlexible ScheduleHealth InsurancePaid Time OffRetirement Benefit

CDA credential required
Prior childcare or preschool leadership experience preferred
Strong knowledge of New Jersey licensing standards
Experience supporting teachers and classroom operations
Excellent communication and organizational skills

SmartExplore AI is experimental.

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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.