Regulatory Affairs Associate
Akkodis
Akkodis is seeking a Regulatory Affairs Associate for our Contract position with a direct client. Position : Regulatory Affairs Associate Location : Portland, ME Duration : 12 months Pay Range: $20/hr - $20/hour on W2 without benefits (Pay rate varies based on experience) We are seeking an experienced Regulatory Affairs professional to support global medical device registrations and ensure compliance throughout the product lifecycle. The role will be responsible for preparing and managing regulatory submissions, registrations, post-market compliance activities, and regulatory documentation while partnering with cross-functional teams including R&D, Quality, Manufacturing, and Marketing. The ideal candidate will have strong knowledge of medical device regulations, regulatory submission requirements, product registrations, and regulatory documentation management. This individual will serve as a regulatory liaison, support regulatory strategy activities, monitor changing regulatory requirements, and help ensure timely approvals and continued compliance of marketed products across global markets. Key Responsibilities: Prepare, coordinate, and maintain regulatory submissions, registrations, amendments, and reports. Support pre-market and post-market regulatory activities for medical devices. Monitor global regulatory changes and assess business impact. Maintain product registrations, licenses, approvals, and facility registrations. Collaborate with internal stakeholders on regulatory strategy, product changes, labeling, and compliance requirements. Support SOP development and regulatory process improvements. Ensure accuracy, quality, and completeness of regulatory documentation. Act as a regulatory representative throughout the product lifecycle. Education: Major/Field of Study or Equivalent Technical Diploma (high school or equivalent) Preferred Qualifications: Experience in Medical Device Regulatory Affairs. Knowledge of global regulatory requirements and submission processes. Strong documentation, project coordination, and stakeholder management skills. Ability to work independently and manage multiple regulatory activities simultaneously. Equal Opportunity Employer/Veterans/Disabled Benefit offerings available for our associates include medical, dental, vision, Life Insurance, short-term disability, additional voluntary benefits, an EAP Program, computer benefits, and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may eligible for paid leave including paid sick leave or any other paid leave required by federal, state or local law, as well as Holiday pay where applicable. Disclaimer: The benefit of offerings do not apply to client recruited jobs and jobs that are direct hires to a client. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers #J-18808-Ljbffr
$20 - $22 per hour
...Regulatory Affairs AssociateContract role for client at South Portland, ME.Position Details: Regulatory Affairs Associate- South Portland, ME Location: South Portland, ME – 04106 Project Duration: 12 Months of contract (Possibility of Extension) Shift Timings: 7:00 AM...SuggestedHourly payPermanent employmentContract workWork experience placementShift work- ...Experis is seeking a Regulatory Affairs Associate to join our team in South Portland, ME, onsite only. The role focuses on assisting in the development and submission of product registration documentation, coordinating regulatory submission packages, and maintaining global...Suggested
- ...Akkodis is seeking a Regulatory Affairs Associate for a contract role based in Portland, ME. The role focuses on supporting global medical device registrations and maintaining regulatory documentation throughout the product lifecycle. The candidate will prepare submissions...SuggestedContract work
$20 - $23 per hour
...Job Description Job Description Regulatory Affairs Associate – Medical Devices / IVDR Location: South Portland, ME Schedule: Monday–Friday, 7:00 AM–4:30 PM Pay Range: $20.00–$23.00 per hour Employment Type: Full-Time Contract Contract Duration:...SuggestedHourly payFull timeContract workWork experience placementWork at officeMonday to Friday- ...Compliance Professional To assist our hedge fund clients and their investors in responding to new regulations and regulatory best practices, particularly in the areas of Anti-Money Laundering and FATCA compliance, we are seeking a compliance professional to join our...SuggestedWork at office
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