Tracks and reports on status of all project deliverables per the approved project schedule. Plans and executes one or more simultaneous project(s) from initiation through delivery. Organizes cross-functional activities, ensuring completion of the project while adhering to budget, scope and schedule ...
Responsible for the preparation and compiling of document packages for regulatory submissions, audits and inspections. Manage and maintain regulatory databases and technical files. Reviews materials such as labeling, marketing materials or user manuals to ensure compliance with regulatory agency req...
As a Robotics Program Manager, you will play a pivotal role in the integration of robotics automation within our organization. Work today, get paid tomorrow through our earned wage access program*. Program Management and Stakeholder Communication:. Soft Skills/Competencies: · Excellent oral and writ...
The Regulatory Affairs Specialist will work closely with the Director of Regulatory Affairs to obtain and maintain global regulatory approvals to allow IPG to market its state of the art devices worldwide. Senior Regulatory Affairs Specialist #24-150 | Posted 07/24/2024 Marlborough, Massachusetts Ap...
Responsibilities for preparation and submission of global regulatory applications, as well as maintenance of internal regulatory file documentation. May lead small projects or represent Urology Regulatory Affairs on corporate teams, as needed. Regulatory Affairs or related experiences. Come join a g...
Principal Regulatory Affairs Specialist - Endoscopy. This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. Acts as a core team member on develo...
Principal Regulatory Affairs Specialist – Endoscopy. This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. Responsible for preparation and subm...
We have a robust pro Regulatory Affairs, Regulatory, Specialist, Principal, Product Development, Support, Business Services. ...
NPI Technical Program Manager, Deployment Readiness. The WW Technology Deployment org is seeking a talented and solutions-oriented NPI Technical Program Manager to contribute to delivering transformational innovation to the business. Experience managing programs across cross functional teams, buildi...
Principal Regulatory Affairs Specialist - Endoscopy. This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. Acts as a core team member on develo...
BELFOR Project Managers have either a restoration or construction focus. Qualified candidates will be the industry expert and are local, regional, or national BELFOR resources for large projects, complex projects, and high-risk/high-profile environments. Project Managers are eligible to become BELFO...
Principal Regulatory Affairs Specialist - Endoscopy. This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. Acts as a core team member on develo...
The IT Governance, Risk, and Compliance Specialist will play a key role on the iboss team by aligning security initiatives with enterprise programs and business objectives. The IT GRC Specialist will make an impact on iboss’ security program and services through experience with various areas includi...
We expect the Manager, Regulatory Affairs CMC to join a growing team and provide support to interpret the current, approved and planned clinical regulatory landscape by contributing to the regulatory submission form process. May act as a submission compliance liaison with other areas of Regulatory A...
Regulatory Manager, Regulatory Affairs - CMC (Gene Therapy). Plans and prepares CMC regulatory packages, assesses changes for potential regulatory impact, responds to action letters, and maintains filings and approvals. Acts as CMC regulatory lead or deputy for complex projects/products, requiring a...
Program Managers oversee the day-to-day operations of residential program, providing leadership, guidance, and clinical support. The program manager also manages the staff schedule to ensure program coverage and serves on-call as needed. The program manager monitors trainings for all program staff a...
Amazon’s Offensive Security, Penetration Testing Team is seeking a Program Manager (PM) to help keep Amazon's applications and services secure for its customers. You’ll be using your program and project management skills to continually improve and mature the program, orchestrate penetration testing ...
CRJ wants you to join our growing team of compassionate and dependable Assistant Program Manager to support the wonderful individuals we serve!. BH provides domestic violence treatment and education, community reentry services, mentoring programs, and intensive outpatient programs. Coordinates and s...
Food Safety Compliance Specialist to assist the Food Safety Manager with ensuring compliance with all food safety and sanitation laws and regulations in assigned store locations. The Food Safety Compliance Specialist’s goal is to maintain a food-safe and healthy environment for all customers, associ...
This includes developing and implementing regulatory strategies for product approvals, leading the registration of products, ensuring compliance with global regulatory requirements, and managing the regulatory affairs team. Title: Regulatory Affairs Manager. The Regulatory Affairs Manager will be re...
Individual Contributor responsible for QA Compliance Strategy for clinical and pre-commercial cell and gene therapies. Oversees contract manufacturing organizations (CMOs), monitoring information requests, reviewing CMO work, and following up on compliance-related items. Develops compliant Quality p...
Proven experience with Python, R, SQL, and a data visualization program like Tableau or PowerBI. Communities, school districts, special education programs, and regional transit authorities count on our companies to get people where they need to go safely and on time. In 2018, Beacon Mobility was acq...
Regulatory Manager, Regulatory Affairs - CMC (Gene Therapy). Plans and prepares CMC regulatory packages, assesses changes for potential regulatory impact, responds to action letters, and maintains filings and approvals. Acts as CMC regulatory lead or deputy for complex projects/products, requiring a...
Facility Engineering Compliance Specialist. Facility Engineering Compliance Specialist . The Facilities Compliance Specialist will be part of the Facility Engineering department supporting the Manufacturing, lab, warehouse, and administrative areas. The Facilities Compliance Specialist is responsibl...
This Compliance Specialist will perform critical QA compliance tasks in support of GMP manufacturing programs as AIRM moves through clinical trials and commercialization. The successful candidate will foster compliance across a broad range of Quality Assurance areas and will work closely with talent...