Trabajos regulatory en New Brunswick, NJ - Page 5Crear alertas

Responsibilities: Autonomously support new product development core teams including development of regulatory strategies and the preparation of regulatory content for domestic and international submissions for IVD medical devices to support the core team's approved scope of regulatory activities,...

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

Provides verbal recognition and acceptance to children while providing clear and consistent expectations for the children's behavior. Must meet the basic requirements of the local child care regulatory agency. Observes all rules and regulations at Primrose School of North Edison and the local, st...

Regulatory expertise to read and interpret global GXP regulations, as well data integrity expectations expertise performing test scripts, traceability matrices, risk assessment and other validation deliverables, review. LabWare) quality assurance mindset for computer system validation for GxP spa...

Responsibilities: Carry out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws.Ensure compliance with current Good Manufacturing Procedures (cGMP), USP, EU and other global regulatory requirements at all times.Follow directions properly,...

Specific job responsibilities responsible for performing validation of computer systems, process automation, equipment, utility systems, and/or facilities by following approved standard operating procedures (SOPs), current Good Manufacturing Practices (GMPs) and all other regulatory requirements ...

The Associate Director, Medical Writing is responsible for the complete preparation, including but not limited to, the writing, reviewing, and editing of Protocols, Investigator Brochures (IBs), Clinical Study Reports (CSRs), and Clinical Summary Modules for regulatory submissions. Successful tra...

Reporting to the Sr Director, Quality Assurance - Pharmacovigilance, the Manager of Pharmacovigilance Quality Assurance serves as a strategic partner managing quality and regulatory compliance related to Good Pharmacovigilance Practices (GVP) and other related activities performed by Drug Safety ...

Promote a culture of continuous improvement, utilizing risk-based approaches and quality metrics to enhance product quality, process efficiency, and regulatory compliance in alignment with Corporate Quality initiatives. Represent Quality across all levels of the organization, including the Leader...

Director of Clinical Quality Assurance, the Director of Clinical Quality Assurance (CQA) serves as a strategic leader managing quality and regulatory compliance related to GCPs, acts as quality lead on the clinical development team, and collaborates on other related activities performed by Clinic...

Company: Everest Global Services, Inc. Strong understanding of the global reinsurance market and the relationship between catastrophe modeling, underwriting, pricing, and capital management. Familiarity with regulatory frameworks in key global markets (e.

Job DescriptionCompany Description BEUMER Group is an international manufacturing leader in intralogistics in the fields of conveying, loading, palletising, packaging, sortation and distribution technology. BEUMER Group offers the right solution for almost every logistic challenge. We are a fam...

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 cli

Complete media relations activities around clinical data, medical congresses, and regulatory achievements, including press material development, spokesperson prep, interview coordination, media monitoring, and reporting. Identify and prepare patient ambassadors to share their stories through earn...

This position is responsible for the preparation of regulatory submissions required to market medical devices in both the and Europe, support of international product registrations and related regulatory affairs activities, including execution of procedures and systems designed to ensure that the...

The position is responsible for day-to-day coordination with Regulatory, Manufacturing/Packaging, MSTG, Quality Unit, Product Development & Project Management HOD’s as well as Managers. Collaborates, coordinates & educates/mentors the ODR-India and ODR-US teams as well as cross-functional departm...

The Registered Nurse provides nursing care in the health care system within the scope of practice defined by the Nurse Practice Act and regulatory standards and assures awareness of ethical standards of practice as defined by the ANA code of ethics. The Registered Nurse is responsible for supervi...

Report all significant matters, issues and unusual customer activity to Manager maintaining personal knowledge of compliance and regulatory requirements.

Complete media relations activities around clinical data, medical congresses, and regulatory achievements, including press material development, spokesperson prep, interview coordination, media monitoring, and reporting. Identify and prepare patient ambassadors to share their stories through earn...

The Registered Nurse provides nursing care in the health care system within the scope of practice defined by the Nurse Practice Act and regulatory standards and assures awareness of ethical standards of practice as defined by the ANA code of ethics. Health Care/Dependent Care Flexible Spending Ac...

Provide direct patient care or direction and supervision to other health team members to ensure proper implementation of care in accordance with the requirements of the NJ Board of Nursing, current regulatory guidelines, the ANA Code of Ethics and institutional policies and procedures. You can ta...

The ideal candidate will have a solid understanding of cybersecurity frameworks, regulatory requirements, risk assessment methodologies, and emerging threats.

Regulatory Studio CMS Senior Manager. Collaborate cross-functionally with Regulatory Affairs and CMC functional teams. Support development of CMC regulatory strategies for.

The Director, Quality Assurance – GxP (GCP) is responsible for managing GxP Quality Assurance (QA) functions with an emphasis on Good Clinical Practice (GCP), compliance for both clinical and marketed products. The Director, Quality Assurance – GxP (GCP) ensures adherence to relevant regulatory

The Department of Emergency Medicine at Rutgers Robert Wood Johnson Medical in New Brunswick is seeking a full-time. The Director will be responsible for administrative supervision of all medical services performed in the RDU, managing the RDU per organizational and regulatory guidelines, and ove...

The DMV Clerk ensures the accurate and efficient processing of vehicle titles by verifying title information is correct, maintaining knowledge of current laws regarding vehicle titles, and interacting with customers and regulatory agencies to resolve title issues.Processes vehicle titles with pre...

We are looking for a highly skilled.In this role, you will provide expert guidance on corporate tax matters, cross-border structuring, regulatory compliance, and transfer pricing for a global business.You will support strategic decision-making across business units and help ensure the group’s ope...

The Director is responsible for planning, directing, coordinating and implementing all aspects of the Regulatory compliance programs and assist with the planning, directing, coordinating and implementing of the Quality program at Robert Wood Johnson University Hospital.

The Emergency Management Specialist will assist the Emergency Management Director and Emergency Management Assistant Director with RWJBH affiliate support related to planning, training, exercising, logistics and regulatory surveys. NJ Certified Emergency Manager (CEM) or IAEM (CEM) or FEMA Emerge...

Collaborates with Service Line Managers to ensure the highest quality of care is provided and is in compliance with federal, state, and local regulatory requirements,. The Operations Manager demonstrates the ability to direct and delegate the daily operations of the assigned unit department utili...

Maintain strong relationships with external modeling vendors, regulatory bodies, industry groups, and other stakeholders to ensure the company stays at the forefront of global catastrophe modeling practices. The leader will be tasked with leading a cross-functional team, working with internal sta...

Writes technical documents such as methods, specifications, method validation protocols and reports, method transfer protocols and reports based on corporate policies and SOP's, compendia, ICH and FDA regulatory guidance.

The Registered Nurse provides nursing care in the health care system within the scope of practice defined by the Nurse Practice Act and regulatory standards and assures awareness of ethical standards of practice as defined by the ANA code of ethics. The Registered Nurse is responsible for knowled...

The Registered Nurse provides nursing care in the health care system within the scope of practice defined by the Nurse Practice Act and regulatory standards and assures awareness of ethical standards of practice as defined by the ANA code of ethics. Float pool nurses have proven to be a valuable ...

Ensure complaints are processed in a timely manner and in compliance with regulatory requirements (e.

Job Description Summary: The Associate Director, Statistical Programming provides technical leadership and operational oversight for the statistical programming activities required to support multiple clinical development programs, the associated clinical studies and regulatory submissions. The A...

AML Compliance Analyst role in the Edison, NJ area. BSA/AML Compliance Analyst responsibilities include:. Maintains current on BSA/AML/OFAC news and events as well as regulatory updates.

Autonomously support new product development core teams including development of regulatory strategies and the preparation of regulatory content for domestic and international submissions for IVD medical devices to support the core team's approved scope of regulatory activities, with focus on ins...

Proven understanding of aseptic techniques and cell manufacturing. Four (4) years of relevant experience in a manufacturing, medical, and/or laboratory environment. Regulatory knowledge of pharmaceutical manufacturing.

In this role, you will optimize the operational systems and processes of the company, maximizing efficiency and profitability while remaining compliant with all legal and regulatory requirements.The ideal candidate has an analytical mind, a deep understanding of business and financial principles,...

The Registered Nurse provides nursing care in the health care system within the scope of practice defined by the Nurse Practice Act and regulatory standards and assures awareness of ethical standards of practice as defined by the ANA code of ethics. The Registered Nurse is an individual practitio...

Under the supervision of the Chief Executive Officer, the QAPI Specialist will support company-wide initiatives to maintain the highest standards of quality care and ensure adherence to regulatory requirements specific to substance use disorder treatment and general healthcare practices.Facility ...

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. Regulatory Affairs or related coursework. With minimal guidance, ensu...

Develop, implement, and oversee comprehensive safety policies and procedures aligned with industry best practices and regulatory requirements. Be the primary point of contact for all safety-related matters, including regulatory compliance, employee training, and emergency response planning.

Advanced knowledge of regulatory requirements related to pharmaceutical manufacturing and 21 CFR requirements. This position shall ensure regulatory compliance of all Sun sites, with products distributed in the US market, for Field Alert Reports and Drug Product Recalls. Experience conducting Tec...

Assist in responses to any internal audit, corporate audit, or regulatory audit observations involving Quality Control.

Manage and coordinate activities associated with the GxP IT Quality Assurance (QA) program for GPS and R&D computerized systems regulatory compliance across the end-to-end product lifecycle (GPS and R&D) for software development and validation lifecycle activities associated with regulated comput...

Job Title: Data Integrity Manager. It is responsible for providing support to the Lead of the GxP Data Integrity program across the end-to-end product lifecycle, ensuring that regulatory and CLIENT requirements are thoroughly and effectively addressed promptly. IT, Computer System Validation, Res...