761 Connor Group Global Services Llc jobs in New Jersey

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CDL Class A Driver - Lambent Logistics LLC

LAMBENT LOGISTICS LLC

Woodstown, NJ 08098

$24/hr

OnsiteUrgently HiringHealth InsurancePaid Time Off

Must be at least 21 years old
Have a valid Class A Commercial Driver License (CDL)
Must Successfully Pass DOT Physical
Must be able to speak, read, and write in English to communicate with the general public, to understand highway traffic signs and signals in the English language, to respond to official inquiries, and to make entries on reports and records
No current CDL suspension or revocation
Clean Motor Vehicle Record (MVR) & good DAC Report
Successfully pass a background check and have a clean MVR
Must pass a DOT physical and pre-employment drug screen
Ability to effectively learn and operate a GPS
Must be able to use handheld technology and smart phone applications
Must be flexible with work schedule (Day/Evening/Night shifts/Weekends)

SmartExplore AI is experimental.

New, Posted 2 hours ago

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Nurse Professional Development Specialist - Center For Ambulatory Surgery Pacu/ Dar - P/t With Benef

Hackensack Meridian Health

Hackensack, NJ 07601

$66,560/yr

OnsiteUrgently HiringEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Graduate Degree (Master's or greater) in Nursing or related field. If the graduate degree is in a related field, must have a baccalaureate degree in nursing.
Graduate of an NLN/AACN accredited program in nursing.
Minimum of 3 or more years of current experience in Nursing in acute setting
Excellent written and verbal communication skills.
Proficient computer skills that may include but are not limited to Microsoft Office and/or Google Suite platforms.
Magnet Recognition Program knowledge.
Must acquire and maintain competencies, certifications and continuing education in order to meet any facility accreditation or individual licensing requirements for areas assigned. This may include Advanced Cardiac Life Support (ACLS), Neonatal Resuscitation Program (NRP), and Pediatric Advanced Life Support (PALS).
NJ State Professional Registered Nurse License.
AHA Basic Health Care Life Support HCP Certification.

SmartExplore AI is experimental.

New, Posted 1 day ago

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Sales Executive

Capelli Sport

South Hackensack, NJ 07606

$75,000-$80,000/yr

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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.

SmartExplore AI is experimental.

New, Posted 1 day ago

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Sales Support Assistant, Group Sales

Six Flags

Old Bridge, NJ 08857

New, Posted 5 hours ago

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Litigation Attorney

Krompier Law Group LLC

Parsippany, NJ 07054

$80,000-$90,000/yr

New, Posted 2 hours ago

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In-Home Sales & Tech Support (Part-Time)

ASURION INSURANCE SERVICES

Orange, NJ 07050

$25.85/hr

Onsite

A valid driver's license and satisfactory driving record with at least 1 year driving experience
A personal vehicle (excluding motorcycles)
Proof of valid car insurance
The maximum expected travel distance is 120 miles, one-way
Work a varied 5-day week schedule designed to meet customers on their timeline –this will include evenings, weekends and holidays
A personal cellphone
Must be comfortable working around household pets
Base hourly rate is guaranteed for all hours worked and paid bi-weekly. Earned pay can now be accessed early!

SmartExplore AI is experimental.

ResumeLibrary

Sales Support Assistant, Group Sales

Six Flags

Allentown, NJ 08501

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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.