Regulatory affairs specialist jobs in Hackensack, New Jersey (NJ) State

Responsibilities include managing the entire contract development lifecycle, as well as ensuring corporate regulatory and license compliance requirements are met. Proven track of success in legal compliance, including a strong grasp of legal terms and conditions, to ensure that contracts, regulat...

Maintains accurate contractual and compliance records for organizational efficiency and legal compliance, often using electronic tools/systems to store documents securely. Summary/objectiveHudson Technologies is seeking a highly motivated contracting and compliance professional with a minimum of ...

Risk and Controls Program ManagerRutherford, NJHybridContract$73/hr - $78/hrGrow your career as a Risk and Controls Program Manager with an innovative global bank in Rutherford, NJ. Escalate program risks to the Program Director, or Program Sponsor, when appropriate. What You Will Be Doing**+...

DutiesWHAT IS THE SMALL BUSINESS/SELF EMPLOYED (SBSE) DIVISION?A description of the business units can be found at: https://www.Vacancies will be filled in the following specialty areas: Small Business Self Employed Field ExaminationThe following are the duties of this position at the full workin...

For the HR Compliance Specialist position, this role will require creating and maintaining policies and procedures. The position will plan, direct, or coordinate activities for the company to ensure compliance are within ethical and regulatory standards including ACA, HIPAA, and more. Collaborate...

You will support all regulatory-related activities, including but not limited to: researching industry updates pertaining to labeling compliance; supporting the review processes for packaging, marketing materials, and digital information. Research and consult on food labels, packaging, and other ...

Regulatory Affairs Labeling Associate Level I is needed to support Client business to prepare and review regulatory labeling deliverables based on Reference Listed Drug labeling, FDA Guidance, regulation and Client internal practices. Applying strategic thinking, pharmaceutical educational kno...

Our client, a Reputable, Global Pharmaceutical Company, is seeking a Regulatory Affairs Strategy professional at the Director level. The position will report directly into the VP of Regulatory Affairs. Develop and implement Regulatory Affairs strategy for Oncology programs. Regulatory Affairs Str...

Joining an established & small Medical Device company, within quality team with both sustaining and new product activities in the pipeline, the Senior Design Assurance Engineer position will give someone the opportunity to lead and mentor quality members, and take the reigns on all design quality...

Role: Quality Engineer - Mobile Testing (. ...

The Quality Engineer is responsible for ensuring optimal production quality performance by addressing quality issues, implementing corrective actions, and maintaining adherence to quality management systems. We are working with a global sing-use medical device company looking for a Quality Engine...

We are seeking a highly skilled and experienced Real Estate and Construction Project Manager with. They will be responsible for coordinating and managing all project activities from inception to completion, ensuring that projects are completed on time, within budget, and to the highest quality st...

The QA & DEA Compliance Coordinator is responsible for maintaining all administrative controlled substances activities, including all reports and quotas, maintain all controlled substance certificates, performs duties of the QA & compliance associates as required. Reports to Senior Manager of Qua...

The Project Manager is the project leader and will drive projects forward through strong collaboration, with a quality and results-driven mindset. The Project Manager is responsible for the overall coordination, implementation, execution and completion of product development projects ensuring con...

As a Construction Project Manager at Spotless Brands, you'll play a pivotal role in driving the development of new car wash facilities in the New York/New Jersey market, specifically supporting Flagship Car Wash. Work with the Pre-Construction Project Manager during this phase. From initial feasi...

Regulatory affairs strategy experience and understanding of CMC, nonclinical and clinical development. Responsible for developing and implementing short and long term global regulatory strategies that support the success of investigational and marketed pharmaceutical products throughout their lif...

Ability to author clear and concise regulatory documents (CMC authoring) with oversight of all documents for regulatory submissions and associated messaging. Ensure development programs are compliant with ICH regulatory requirements and all local country regulatory requirements. Work closely with...

Specialist Regulatory Affairs Fort Lee , New Jersey Apply Now. Specialist for Regulatory Affair. As the US Product Owner (USPO), responsible for the maintenance of the US dossiers and the execution of lifecycle and regulatory compliance activities of the assigned licensed products in line...

Coordinates the collection of documents, records, reports, and data from the Development, Clinical Affairs, Quality, and Operations Departments for inclusion in regulatory documents. Responsible for the coordination and preparation of document packages for regulatory submissions from all areas of...

The Staff Regulatory Affairs Specialist will work in BD Medical - Pharmaceutical Systems Business Unit taking on a lead role at the project level in developing and executing regulatory strategy and compliance plans to promote and support drug delivery solutions for pharma combination product deve...

Regulatory and QA Specialist Our client is a highly regarded manufacturer of flavors and essential oils. It is located in northern NJ. We have been working with this company for a number of years and ...

Eligibilities & qualifications....

Prepare new and maintain existing regulatory files in accordance with regional requirements, including but not limited to document updates, management of regulatory information in databases, and navigating document control systems. Review regulatory content for completeness, accuracy, consistency...

In lieu of a Master’s degree in Regulatory Affairs and two (2) year of work experience in the job offered or related occupation in which the required experience was gained, employer will also accept a Bachelor's degree in Regulatory Affairs and five (5) years of work experience in the job offered...