Regulatory jobs in New Brunswick, NJ - Page 4Create job alerts

Vibra Travels is seeking a travel Pediatric Speech Language Pathologist for a travel job in East Brunswick, New Jersey. Job Description & Requirements • Specialty: Pediatric Speech Language Pathologist, • Discipline: Therapy, • Duration: 13 weeks, • 40 hours per week, • Shift: 8 hours, days, • ...

Job Description We are seeking a Senior Privacy & Legal Counsel for the US and Canada to oversee WSA’s privacy practices and ensure adherence to applicable local, state, and federal regulations in the region. You will join a dynamic, multicultural international team of over 20 lawyers and report...

Comprehensive Healthcare Benefits. Prefer knowledge in governmental and regulatory guidelines in designated healthcare settings.

Job DescriptionDescription: As a Specialist CDL Driver at Lewis Environmental, you will be a critical part of our team, responsible for driving commercial vehicles to support a variety of Environmental Services projects. Your role will include transporting hazardous and non-hazardous materials, r...

MAINTENANCE MECHANIC New Brunswick, NJ (Onsite) 23583 At Wimmer Solutions, we believe care creates community. We work smart; we have built a reputation for results-oriented, innovative, business and technology solutions that help companies execute on their strategic initiatives. We have ...

We are seeking a hands-on Java Technical Lead who can lead a small team while actively contributing to design, development, and integration work. This role focuses on post-trade processing for regulatory reporting and collatera...

Data Reviewer III—New Brunswick, NJ With minimal direction from management, this individual: • Performs critical in-depth review of all scientific data for Quality Control laboratory documents (including, but not limited to review of raw data of in-process, API/Excipients, Finished Products, ...

Job DescriptionIf you love to make others smile, create a-ha moments, and develop future leaders join our team. As a Lead Infant Teacher, you will: • Be the primary caregivers to our little ones., • Help infants develop their fine motor skills., • Maintain feeding, sleeping, and diaper changin...

Job DescriptionBenefits: • Company parties, • Free uniforms, • Opportunity for advancement, • Paid time off

Plant Manager New Brunswick, NJ $140,000 - $165,000 + bonus opportunities Position Summary: We are seeking a highly experienced and results-driven Plant Manager to lead and oversee all daily operations of our manufacturing facility. You will be responsible for ensuring production effi...

The Pharmacovigilance (PV) Analytics and Reporting Specialist, PV Analytics Center of Excellence is responsible for successful execution, and close-out of activities aligned with the overall vision, strategy, and objectives of the Global Biostatistics & Data Sciences Function. The PV Analytics a...

Job Description Why work for Lightbridge Academy? When you join the Lightbridge Academy family, you become part of a team of lifelong learners passionate about children and families just like you are. As an early childhood education leader, and a key member of our teaching team, you embody the Li...

Overview: Interstate Waste Services is the most progressive and innovative provider of solid waste and recycling services in the country! We primarily service Northern New Jersey, Southern New York State, New York City, Connecticut, with a state-of-the-art rail served landfill located in Ohio. W...

Overview: Interstate Waste Services is the most progressive and innovative provider of solid waste and recycling services in the country! We primarily service Northern New Jersey, Southern New York State, New York City, Connecticut, with a state-of-the-art rail served landfill located in Ohio. W...

Job Description Job Description Date 06/2025 Location 1300 Airport Road, New Brunswick, NJ Title Material Handler Department Warehouse Reports to Manager, Warehouse FLSA (Exempt or Non-Exempt Non-Exempt Role Overview The Material Handler will perform all functions related to rece...

The Regulatory Affairs Lead for the Tactical Implementation Team will lead the regulatory team responsible for the execution of regulatory activities across assigned programs and markets. In collaboration with regulatory strategists, act as regulatory point of contact for cross-functional teams t...

Position Summary / Objective** The CMC Regulatory Senior Manager, Cell Therapy is responsible for content development, compilation, maintenance, and review of the Quality Module for regulatory submissions regarding: Clinical trial applications; New marketing applications; HA responses & backgrou

Europe, support of international product registrations and related regulatory affairs activities, including execution of procedures and systems designed to ensure that the product development process addresses all regulatory requirements as well. Responsibilities: This position is responsible for...

Regulatory Cmc Leadership And Strategy.This position is a key role that will provide regulatory CMC (RA CMC) leadership and strategy to achieve regulatory approvals in various countries.As a strategic function, RA CMC is required to collaborate closely with multiple functions within Insmed and wi...

Job Description Welcome to Distinctive Living, we're seeking a Medication Aide (Full-Time) for our Mira Vie at Warren community! Here at Distinctive Living, we want our people to realize their full potential. We're passionate about personal and professional growth and will do everything we can t...

IB, DSUR, regulatory responses) + Collaborate and serve as primary liaison between external partners for scientific advice Degree Requirements + Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred) Experience Requirements + 5+ years of experience in clini...

Responsibilities: Well versed in performing CMC compliance activities including Gap Analysis; assessment for Annex 3 comparative table with reference EU Member States Manage execution / authoring and review of CMC documentation (Module 1, 2 and 3 / Part II) for life cycle management - post-approv...

Communicates new and emerging technical accounting policy developments and related regulatory developments to managers and executives throughout LFG. Certifications** CPA A+ but not required Education 4 Year/Bachelor's degree or equivalent work experience (4 years of experience in lieu of Bac...

Responsible for handling all food and beverages in accordance with sanitary procedures and standards and complies with all federal, state/provincial, and local regulatory procedures regarding food service. Practice safe food handling at all times to prevent an outbreak of food borne illness. Foll...

Job Description Spectrum Vascular is a leading innovator in vascular access solutions, committed to delivering excellence and advancing patient care. As a key member of our team, the International Sales Support Associate will be responsible for supporting our International Direct and Distributer ...

Job Description Spectrum Vascular is a leading innovator in vascular access solutions, committed to delivering excellence and advancing patient care. As a key member of our team, the Global Customer Experience Analyst will be primarily responsible for monitoring the company's Electronic Data ...

As applicable, all Sunrise team members who drive a Sunrise vehicle must sign the Driver job description and understand the key essential duties for safety and regulatory compliance. This is the 8th time Sunrise has received this top culture and workplace designation, highlighting the special pla...

Responsibilities: The Regulatory Affairs Associate, with minimal guidance prepares, reviews and submits high quality annual reports with FDA within Annual report timelines and in accordance with regulatory guidelines and applicable federal laws. With minimal guidance, ensure to compile and comple...

The Director of Medical Affairs organizes and directs Medical Staff with the Hospital Administration, Chief Medical Officer, Joint Commission, and applicable Federal, State, Local regulatory agencies. Reports to the Vice President of Medical Affairs/Chief Medical Officer, for all work, and suppli...

Essential Functions: + The Regulatory Affairs Specialist, assists in the management of regulatory submissions to (FDA) and other Health Authorities, as required, within company timelines and in accordance with regulatory guidelines and applicable federal laws. Description: The Regulatory Aff

Develop strategic direction and provide leadership for all regulatory interactions with FDA/global regulatory authorities. Develop global or US regulatory strategy for oncology products in development and through life cycle management, considering all relevant guidance, commercial needs, and comp...

Qualifications: Bachelor's degree in Quality Management, Regulatory Affairs, Life Sciences, or a related field.Minimum of 5 years of experience in QMS, quality assurance, regulatory compliance, or related roles.Strong knowledge of FDA and EU regulatory requirements,.

Responsibilities include:** + Accountable for ensuring compliance w/Colgate-Palmolive, local, state, and federal standards and guidelines related to EHS, Quality, and Regulatory + Serve as primary resource to the operations and quality team for issues involving design, process changes and eq

The Senior Scientist - CMC R&D will be responsible for developing study protocols, reports, BLA/IND sections, regulatory meetings packages, briefing books and any other R&D documents required for regulatory submissions and will be the key resource responsible to collaborate between R&D groups (pr...

Two new Regulatory Manager requisitions are about to go live in the system; one based in Princeton, NJ, and the other in San Diego, CA. Job Title: Regulatory Publishing Manager I Duties The Manager/Sr. Manager, Regulatory Publishing is responsible for publishing, QC, and transmittal of eCTD submi...

Job DescriptionBenefits: • 401(k), • Competitive salary, • Flexible schedule, • Paid time off, • Training & development Paramount Pharmacy Group 377 Hoes Lane, suite 201, Piscataway, NJ 08854 Position Type: Full-Time Operational Hours: Mo...

The Associate Scientist II, Biology supports adherence to all regulatory requirements and company Standard Operating Procedures (SOPs) including as appropriate. The Associate Scientist II, Biology is responsible for performing scientific experiments that contribute to research and drug discovery ...

R&D, Operations, Process Engineering, Quality Engineering, Supplier Quality, Regulatory. The Engineer may also participate in process design for manufacture of clinical-grade tissue forms at any stage of product development so that novel tissue forms may be manufactured and released for pilot cli...

Insmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases.Our most valuable resource is our employees, and everything we do is motivated by a patients-first mentality.We are dedicated to growing our team with talented indivi...

Job DescriptionBenefits: • 401(k) matching, • Competitive salary, • Flexible schedule, • Health insurance, • Paid time off, • Training & development Paramount Pharmacy Group 377 Hoes Lane, suite 201, Piscataway, NJ 08854 Position Type: Ful...

Job DescriptionBenefits: • Competitive salary, • Flexible schedule, • Opportunity for advancement, • Paid time off, • Training & development Paramount Pharmacy Group 377 Hoes Lane, suite 201, Piscataway, NJ 08854 Position Type: Fu...

Responsibilities: Provides SAS programming support to all clinical studies.Manages assigned programming CROs providing oversight and appropriate QC for programming deliverables.Provides statistical programming support for regulatory submissions (e.FDA, EMA), including electronic submission standa...

The ideal candidate will be responsible for overseeing and managing critical data related to pharmaceutical product lifecycle, ensuring data integrity, accuracy, and regulatory compliance. Perform regular audits and data reviews to ensure the highest level of data integrity and minimize risk. Con...

Knowledge of the software development life cycle (SDLC) and quality assurance methodologies is essential. Proven ability to identify and address issues during testing, ensuring software meets quality standards. Strong business knowledge of quality, regulatory, manufacturing, and compliance system...

Job Description Job Description Date 06/2025 Location 1300 Airport Road, North Brunswick NJ Title Operator, Compression & Encapsulation Department Standard Manufacturing Reports to Production Supervisor FLSA (Exempt or Non-Exempt Non-Exempt Role Overview The Compression and Enca...

Job Description Job Description Date 11/2020 Location 1300 Airport Road, North Brunswick NJ Title Production Operator Department Standard Manufacturing - Beads Reports to Production Supervisor FLSA (Exempt or Non-Exempt Non-Exempt Role Overview The Beads Operator is responsibl...

Job Description Job Description Date 06/25 Location 1300 Airport Road, North Brunswick NJ Title Operator, Tablet Coating 1 Department Standard Manufacturing Reports to Supervisor, Production FLSA (Exempt or Non-Exempt Non-Exempt Role Overview The Tablet Coating Operator is re...

Nonclinical Regulatory Document And Scientific Writer. Experience reviewing regulatory documents, DMPK and BA reports, and non-GLP/GLP data and notebooks.