Regulatory Affairs Specialist Jobs in Massachusetts
19 Massachusetts Regulatory Affairs Specialist jobs found on Monster.Jobs 1 to 19 of 19
Senior Regulatory Affairs Specialist (Devices) PURPOSE AND SCOPE: This candidate will be responsible for the preparation of regulatory documents (submissions) for new and existing medical device products. Individual may act as FDA liaison for some projects. In addition, this individual will evaluate and comment/advise on change controls and manufacturing for both clinical and commercial products....
Job duties and responsibilities: The Regulatory Affairs Specialist is responsible for identifying, evaluating, and ensuring meaningful compliance with all applicable laws, regulations, and standards. Efforts to ensure company compliance shall be inherently established within the company’s Quality System, the Mevion Business Management System. All RA/QA personnel shall seek to develop a quality and...
MRINetwork™ is the world's largest executive search and recruitment organization. We have a global network of more than 1,000 offices. Management Recruiters - The Boston Group is our 5 office organization, established in 1966 to provide executive and management level staffing services to a wide variety of industries. COMPANY INFO My client manufactures and develops dental, medical and surgical sup...
Click Here to Apply for this Job! Job Summary: This position is primarily responsible for international (specifically Asia) product submission/registration activities. This includes interpretation of relevant government regulations and assisting in establishing compliance to these regulations. Essential Duties and Responsibilities: •Responsible for product submissions, license renewals, periodic u...
Regulatory Affairs Specialist thru Senior Specialist for Medical Device 510k submissions. Two positions available in the Northeast, USA! Live in one of the world's leading innovative hotbeds with tons of lifestyle choices, cultural and outdoors activities available at your doorstep! Join a world leading and growing firm with tons of advancement opportunities and awesome comp & benefits. We will pa...
Company Confidential Danvers, MA, 01923
COMPANY DESCRIPTION NeuroLogica Corporation, a subsidiary of Samsung Electronics, is located in the Boston metro area. NeuroLogica develops, manufactures and markets innovative medical imaging equipment for healthcare facilities and private practices worldwide. Established in 2004, NeuroLogica’s founders have over 100 years of combined experience in the design, development and manufacturing of ima...
Health Care Regulatory Specialist Core Health is a Health Services Management company specializing in managing at-risk patients: the elderly, Medicaid beneficiaries and the Medicare-Medicaid Dually Eligible. We serve integrated health systems, Medicare Advantage Plans and Accountable Care Organizations. The Specialist will provide strategic and project management support to the Corporate Affairs D...
Publishing and Submission Support Specialist Location: Cambridge, MA Job Type: Full-Time Duration: 6 month contract (possible extension) Compensation: Open to discussion Objective: · The Publishing and Submission Support Specialist assumes responsibility for the compilation and publishing of all global regulatory submission types (including eCTD, NeeS, Global Dossier, paper etc.) and undertakes su...
About the company Our client is a global regulatory affairs consulting firms working with leading companies in the biotech, pharmaceutical and medical device industries. Job description Our client is looking for a Senior Regulatory Scientist to Participate as team member for a number of the company's global regulatory projects. The Senior Regulatory Scientist will define and implement regulatory s...
A leading global Biotechnology Organization is currently recruiting for a Project Manager, Regulatory Affairs based in Cambridge, MA. This is a long term 8+ month contract, paying a competitive hourly rate dependant on experience and qualifications. This position is interviewing immediately and can start as soon as possible (notice period is also fine). The Project Manager, Regulatory Submissions,...
Your challenge To contribute to the success of Philips Healthcare by managing Q&R challenges on both product and process level. The key to succeed is to utilize all your professional, technical and personal skills in a dynamic, multi-disciplinary environment Your responsibilities The Quality Specialist is primarily responsible for providing support to Q&R Management on the completion and maintenan...
Organization Overview: Commonwealth Care Alliance is a rapidly growing nonprofit organization providing integrated healthcare and social support services to people with complex medical needs. Our patients are seniors and persons with disabilities covered under Medicaid or both Medicaid and Medicare. Our innovative care model is nationally recognized for its effectiveness in improving health outcom...
The Customer Service Specialist will be the focal point with customers, internal and external, to build and manage trusting working relationships to drive profitable economics for the customer and the Teleflex OEM business. The position will manage activities across multiple functional areas to connect the operational processes and provide the customer with timely and accurate information and prod...
Additional Contract Services is looking to fill a position for Quality Assurance Specialist position in Bedford, MA 1st Shift Temp to Perm $26/hr. Start: Immediately A 45-minute phone interview first, and then an in-person if they pass the phone interview. General Summary: This is a late stage, venture-backed start-up that has taken ground breaking research in the area of gait normalization, devel...
Additional Contract Services is seeking a QA Specialist who has experience with FDA, metric reporting, and able to work in a cross-functional team with Manufacturing and Engineering. Our client has an immediate need to augment the Quality Assurance and Regulatory Affairs team with a QA Specialist. This new addition will be responsible for providing support to a fast-paced organization designing, d...
Respiratory Therapist - Clinical Specialist MUST HAVE HALF A PERSONALITY!!! THIS JOB INCLUDES A LOT OF TIME W/ DR. & HOSPITAL CLIENTS! My client has an exciting and unique full time field based Clinical Specialist Respiratory Specialist position. The Clinical Specialist serves as primary resource for educating customers and potential customers on all aspects of Operating Room protocol, product per...
Teleflex Medical OEM is the leading, global provider of comprehensive product development and production services to medical device manufacturers across the world. We set ourselves apart with deep expertise, decades of experience, and extensive, in-house capabilities, which include engineering, regulatory affairs, prototyping, manufacturing, assembly and packaging. Our customers depend on Teleflex...
ORGANIZATION OVERVIEW: Commonwealth Care Alliance is a rapidly growing nonprofit organization providing integrated healthcare and social support services to people with complex medical needs. Our patients are seniors and persons with disabilities covered under Medicaid or both Medicaid and Medicare. Our innovative care model is nationally recognized for its effectiveness in improving health outcom...
JOB SUMMARY Management of cGMP compliance activities for Quality Assurance – Compliance group in accordance with Organogenesis policies, standards, procedures and cGMPs. Typically manages 5 direct reports and works cross-functionally on a daily basis with Operations, Process/Product Development, Quality Control, and Regulatory. Key Responsibilities Manages the site’s Quality Management System to e...
Pharmalink Consulting - leading providers of reg affairs support
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Regulatory Affairs Associate
$38,760.00 - $94,500.00
Typical Salary for Regulatory Affairs Associate in Massachusetts
Source: Monster.com Careerbenchmarking Tool
Education / Training
Some College Coursework Completed
Source: Monster.com Careerbenchmarking Tool
Regulatory Affairs Associate
Ensures regulatory compliance by determining submissions requirements; assembling and preparing submissions; collecting and providing information.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Accomplishes organization goals by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.
Protects organization's competitiveness by keeping information confidential.
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