The Clinical Manager is responsible for the management and quality assurance of all clinical services of the program, including the training and supervision of all clinical staff. The Clinical Manager is a key leader on the Management Team and works closely with the Senior VP of Clinical Services to...
The project manager will work with other critical facilities specialists to evaluate new and existing server room and other critical environment projects. Project Manager – Critical Facilities Design Build – Marlborough, MA. Their projects are in the design-build areas for Cleanroom Cons...
Renewal by Andersen is looking to add an Install Project Manager to our team in Northborough, MA. Provide support to sales reps with pre-sale site visits to define project scope and ensure the scope of work is reflected in pricing and contract documents. ...
Project Manager - Power Delivery. These consulting services provide clients with overall project management tasks in the areas of comprehensive engineering design of electrical transmission and distribution, substation, and transmission line projects nationwide. Project Manager Responsibilities:. Pr...
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. Come join a growing, global division and become a member of a large and experienced regulatory team!. Acting as company representative, developing and ...
We have a robust pro Regulatory Affairs, Regulatory, Specialist, Principal, Product Development, Support, Business Services. ...
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. 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...
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...
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...
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...
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...
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...
Under the general direction of the Principal Investigator or designee, the Research Program Manager I is responsible for managing the day-to-day operations of NIH or other externally funded, large scale projects. The Research Program Manager will collaborate with investigators, consultants, project ...
CRJ wants you to join our growing team of compassionate and dependable Program Managers to support the wonderful individuals we serve!. Ensure that personal, medical and nursing care, behavior plans, teaching programs and other services are delivered by program staff in an appropriate and consistent...
Establish and implement program management practices and tools to continuously improve project execution, tracking, and reporting across the portfolio. Experience leading complex programs in Jira. ...
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...
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...
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. Regulatory affairs experience in generating applications and experience in collaboration with ...
Leadership in driving continuous and incremental delivery of value to the business • Talent for driving change and continuous improvement • Coaching/mentoring in agile principles to help develop a high performing, agile team • Ability to drive consensus and resolve conflicts across mu...
Assist and ensure program and consumer funds are handled according to HMEA policies and procedures. Maintain day to day operations in Manager’s absence. Ensure the people’s rights, privacy and confidentiality are respected and serve as the program Human Rights Officer. Perform assigned tasks delegat...
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...
The role will be responsible to work through multiple levels within the organization and external stakeholders to influence and drive Waters Quality, Regulatory & Clinical Affairs strategy to support Waters business growth and success of the Clinical organization. Lead the Global Design Quality Assu...