Regional Regulatory Manager - Morrisville, PA

The Regional Regulatory Manager provides environmental and regulatory compliance support to facilities across the Northeast United States.This support includes permitting and filings, as well as regulatory approvals and compliance associated with chemical distribution that touche ...

Capital Health es la líder regional en proporcionar atención médica progresiva con inversiones significativas en nuestros destacados profesionales de la salud, enfermeras y personal excepcionales. · ...

+Job summary · A Regional Regulatory Manager provides environmental and regulatory compliance support to facilities across the Northeast United States. · +4-year degree in Environmental Science, Chemical Engineering, or related subject. · 5+ years of practical experience with env ...

Reporting to the Director, Regulatory Affairs, this position is responsible for managing organizational and programmatic activities related to regulatory processes in the Capital Health Medical Group (CHMG) and governing bodies. · ...

The Global Regulatory Manager will be responsible for all regulatory activities related to assigned products in line with business/R&D objectives. · Drive regulatory processes in line with business/R&D objectives. · Interact with Country Regulatory managers/regional leads regardi ...

We specialize in Contingent hiring Direct Hires Statement of Work Payroll Management IC Compliance RPO and Managed IT Services. · In conjunction with Regulatory Leads coordinate creation and approval of global regulatory plans transmit to internal and external experts to execute ...

The RIM Specialist will be a subject matter expert in the Regulatory Information Management (RIM) system with focus on activities like planning , tracking and monitoring activities related to commercial and investigational products applications/ submissions and registrations. · K ...

The Regulatory Information Management (RIM) Specialist will plan track and monitor activities related to commercial and investigational products applications submissions and registrations. The specialist will interact with regulatory associates globally maintain departmental proc ...

The RIM contractor enters and manages regulatory information for submissions approvals associated product data creates CMC change control content plan feeds DCN CS portal maintenance monitors data quality accuracy integrity participates in system testing upgrades executing script ...

The RIM Specialist will be a subject matter expert in the Veeva Regulatory Information Management (RIM) system with a focus on submissions, · correspondence, registrations and commitments for all products worldwide. · Ensure RIM Inbox requests for correspondence, · commitments an ...

+We are a trusted partner to our customers when it comes to innovation and an industry leader in clean label ingredients, · we are a true partner. · A commitment to Purely Better drives our innovation team to discover new, · on trend solutions. · Manage regulatory oversight for a ...

The Regulatory Manager leads the development, · oversight and execution of regulatory compliance programs across Bonduelle Americas' supply chain in support of business objectives. · ...

Vibrant Ingredients seeks a Regulatory Manager to oversee day-to-day regulatory operations and ensure compliance across assigned product lines. · ...

We are seeking a Scientific Global Regulatory Manager to support our team in the preparation of HA interactions and maintain tracking data for health authority meetings. · Support Regulatory Lead in the preparation of HA interactions (meeting preparation, rehearsals, execution, f ...

+We are seeking a Global Regulatory Manager to join our team. The successful candidate will have experience in regulatory knowledge and procedures. · +Interact with regulatory liaisons... · ...

We believe everyone has an opportunity to lead. We see the importance of your perspective and your ability to create value.We want you to fit inwith an inclusive culture, focus on work-life fit and well-being, and a supportive, connected environment; but we also want you to stand ...

We are hiring for an Urgent HOTJob in Lawrenceville, NJ. Responsibilities will include developing CMC regulatory strategy, preparing submission documents, managing CMC activities related to developmental or commercial compounds. · Experience with CMC regulatory documents (IND/CTA ...

The job involves participating in the development of the regulatory strategy for small molecules, biologics and cell therapy submissions. It also includes preparing and reviewing submission documents and interacting with health authorities. · BS/BA degree in scientific discipline ...

+ Job summary: Regulatory Affairs Manager is responsible for contributing to and implementing regulatory strategies and tactics for the Company. · + Responsibilities:Act as a primary contact for regulatory affairs on cross-functional product development and post-marketing teams. ...

We are seeking a Global Regulatory CMC Manager to join our team! As a key member of our regulatory affairs team, you will be responsible for developing and implementing global regulatory strategies for post-approval small molecule product submissions. · Participate in the develop ...