Regulatory Affairs Associate
Buckeye Global
Applicable Shift Onsite 100% during about 2 months training period; after that, potential for hybrid (3 days onsite, 2 days remote) - training period is subject to change, hybrid is subject to review Job Summary This position will ensure compliance with North American and European requirements for safety data sheet (SDS) and label preparation. Responsibilities include completing hazard assessments of final and intermediate formulations, preparing hazard communication documentation, maintaining product information databases and confirming compliance with health and safety, transportation and waste requirements. Cross‑functional interaction with research and development, marketing and sales and operational facilities is essential. Key Job Responsibilities Maintain competencies in North American (HazCom 2024, WHIMS 2022) and European (CLP) hazard communication requirements. Assess, classify and author safety data sheets (SDS) using SAP Product Compliance authoring solution. Prepare SDS in multiple regional formats and according to local language requirements. Review raw materials and associated toxicology/ecotoxicology information to confirm appropriate classification of mixtures. Enter hazard information into SAP based system to provide compliant labeling to research and operations facilities. Perform transportation reviews to ensure appropriate classification of hazard materials/dangerous goods and associated packaging requirements. Maintain internal hazard database to communicate information to all internal areas of the company. Perform periodic audits to ensure hazard communication and transportation data accuracy and quality. Assist in review and update of SDS from contract and 3rd party manufacturers. Provide internal support for questions concerning hazard assessments, transportation classification and waste management. Maintain knowledge of domestic and international chemical inventories and lists for populating regulatory information section of SDS. Maintain transportation (DOT, IATA, IMDG) certifications. Assist in developing and updating procedures on SDS processes. Qualifications/Requirements Bachelor’s degree in chemistry, engineering, environmental studies, or other science‑based program 1+ years' industry experience Nice to have: 1 – 2 years’ experience in safety data sheet (SDS) authoring and regulatory compliance Nice to have: Experience with SAP Product Compliance/EHS module as well as experience with Microsoft Office programs Ability to interact with multiple departments and personalities Ability to maintain self‑motivation in independent work atmosphere. Ability to effectively manage multiple projects and prioritize workload. Strong communication, time management skills; team player #J-18808-Ljbffr
$29.42 per hour
...Overview The Fountain Group is currently seeking a Regulatory Affairs Associate I for a prominent client of ours. This position is located at Clark, NJ. Pay Rate: $29.42/Hour Duration: 6 months Shift Details: Hybrid is dependent upon candidate engagement, reactivity,...SuggestedShift work$30 - $36 per hour
...Job Title: Regulatory Affairs Associate I Position Type: Contract (12+ Months) Location: Clark, NJ 07066 Salary Rate: $30–36/hour Job Description We are seeking a detail-oriented Regulatory Affairs Associate I to support regulatory compliance activities for products distributed...SuggestedContract workWork experience placement- ...Overview Job Title: Regulatory Affairs Associate I Location: Clark, NJ 07066 Duration: 06 months Job Profile Summary Maintain competencies in North American (HazCom 2024, WHMIS 2022) and European (CLP) hazard communication requirements. Assess, classify and author safety...SuggestedLocal area
- ProKatchers LLC is looking for a Regulatory Affairs Associate I in Clark, NJ. The ideal candidate will maintain compliance with North American and European hazard communication requirements, assess and author safety data sheets (SDS), and prepare these documents in multiple...SuggestedContract work
$29.42 per hour
Overview The Fountain Group is currently seeking a Regulatory Affairs Associate I for a prominent client of ours. This position is located at Clark, NJ. Pay Rate: $29.42/Hour Duration: 6 months Shift Details: Hybrid is dependent upon candidate engagement, reactivity...SuggestedShift work$29.42 per hour
A prominent staffing agency is seeking a Regulatory Affairs Associate I to support a client in Clark, NJ. The role involves reviewing raw materials for regulatory compliance, tracking global regulations, and supporting product registrations. Candidates should have a Bachelor...Hourly pay- Buckeye Global in Clark, New Jersey is seeking a professional to ensure compliance with safety data sheet preparation and related documentation. The role involves assessing formulations, preparing documentation, and maintaining databases across various departments. The ...
- ...A leading regulatory compliance firm is seeking a detail-oriented Regulatory Affairs Associate I to support compliance activities for products distributed in the United States and Canada. The role involves reviewing product formulas and artwork for regulatory compliance...Contract work
- ...Europe and Asia enables us to be a powerful contributor and connector of right Talent. Job Description Description: The Regulatory Affairs Associate, with minimal guidance prepares, reviews and submits high quality annual reports with FDA within Annual report timelines...
$70k - $75k
...The Regulatory Compliance Associate, in this highly detail‑oriented role, is responsible for coordinating the workflow of domestic and international product labeling projects, maintaining all project documentation, obtaining required approvals, and communicating new and...Full timeWork at office- ...Role: Regulatory Affairs Associate Location: United States Duration: Long Term contract Position Summary We are seeking a detail-oriented Regulatory Affairs Associate to support regulatory activities for medical devices, pharmaceuticals, biotechnology products, or combination...Long term contract
$70k - $75k
...Regulatory Compliance Specialist Base pay range: $70,000.00/yr - $75,000.00/yr The Regulatory Compliance specialist, in this highly detail... ..., ingredient specifications, and certifications. The associate also supports regulatory and customer compliance programs, religious...Full timeWork at officeImmediate start- Stark Pharma is looking for a detail-oriented Regulatory Affairs Associate to support regulatory activities for medical devices and pharmaceuticals. You will prepare and submit regulatory documentation, maintain compliance, and assist with FDA submissions to ensure adherence...
- ...The Regulatory Affairs Sr. Associate is an experienced medical device regulatory professional who can independently support and, where appropriate, lead regulatory activities across the product lifecycle. This role is intended for a stronger candidate with hands-on experience...Work at office
$20.85 per hour
...selected candidate will be required to submit to a name-based and fingerprint-based criminal history record check. There will be a cost associated with this process for new employees. No cost is associated with this process for existing DMV employees. Related program...Hourly payPermanent employmentTemporary workWork experience placementWork at officeMonday to FridayNight shift- ...and GLP auditing experience. The role involves conducting audits, reviewing bioanalytical studies, and ensuring compliance with regulatory standards. Strong communication and organizational skills are essential, along with at least 5 years of experience in the field....3 days per week
$20.85 per hour
A state government agency in New Jersey seeks a Driver License Examiner to administer eligibility tests for various licenses. This role involves high volumes of transactions, checking vision, and evaluating driving skills. Candidates should possess a valid North Carolina...Hourly payTemporary work$173.2k - $272.6k
...training integration. Proficiency with data governance, AI risk assessment, and compliance monitoring. Knowledge of medical ethics, regulatory compliance audits, and pharmaceutical compliance. Adaptability, decision‑making, and project risk assessment skills....For contractorsWork at office- A leading staffing solutions provider in New Jersey is seeking a Regulatory Affairs Associate to prepare and submit annual reports to the FDA. The ideal candidate will have a Master’s degree in Science and at least 3 years of experience in the pharmaceutical industry....
$80k - $96k
...goal is simple–do what's right for patients, surgeons, tissue donors, and their families through our guiding principles. The Regulatory Affairs Specialist is responsible for working with product development and manufacturing management to ensure that the product development...Temporary workWork at officeLocal areaMonday to FridayFlexible hoursShift work- ...company based in Clark, New Jersey, is looking for a highly organized Color and Artwork Developer II. This role involves managing regulatory artwork projects from inception to approval, ensuring compliance within the artwork management system (TAG). The ideal candidate...
- ...The incumbent in this individual contributor role ensures the compliance of equipment and the ECQ group with local, global, and regulatory guidelines. The incumbent will perform periodic reviews of equipment, policies and procedures, gap analysis where required, and small...Work at officeLocal area
- Dormont Manufacturing Co is looking for a Trade Compliance Analyst to support import/export operations. This position involves ensuring compliance with U.S. regulations, partnering with customs brokers, and maintaining data integrity within trade systems. Qualified candidates...
$61.5k - $88.5k
...determination and documentation). Drive data quality improvements between Oracle ERP/Fusion and GTM to reduce clearance delays and rework. Regulatory & OGA Coordination Coordinate compliance requirements across applicable Partner Government Agencies (e.g., FDA, EPA, USDA),...Work at office- ...The Compliance Coordinator is responsible for supporting regulatory compliance operations for Huber Winery, Starlight Distillery, and... ...accurate, and compliant with federal regulations. Qualifications Associate’s or Bachelor’s degree in Business, Accounting, Compliance,...Work at officeLocal areaMonday to Friday
- ...support in the interpretation of regulations and the Bank's policies and procedures and disseminate information on matters affecting regulatory compliance, including consultation with management and teammates on compliance-related issues. Maintain knowledge of consumer...
- Solomon Page is seeking a Clinical Data Analyst for an onsite role in Clark, New Jersey. The ideal candidate will possess a Bachelor’s degree and at least 3 years of lab and research experience. Responsibilities include hands-on lab work, data analysis, and creating technical...Contract work
$70k - $75k
A leading food manufacturer is seeking a Regulatory Compliance Specialist to coordinate product labeling projects and maintain compliance documentation. The ideal candidate will have an associate degree and at least 3 years of experience in quality assurance within a food...Full time$70k - $75k
A food manufacturing firm is seeking a Regulatory Compliance Associate in Kenilworth, New Jersey. This role focuses on coordinating product labeling projects and ensuring compliance with regulations. Candidates should have an associate degree, at least 3 years of experience...Full time- Job Title Individuals will be handling multiple activities in a team supporting diverse NA Scientific data needs. Will be in the R&I group (Research and Innovation) Primary Functions Data architecture, data development and design, data quality management, reference...
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