Regulatory Affairs Associate
Virtual Vocations Inc
Seeking a skilled Regulatory Affairs Associate, this remote contract position will manage and optimize the preparation, publishing, and electronic submission of regulatory documents for global diagnostic products, ensuring compliance with U.S. and EU regulations. Key Responsibilities Lead the preparation and electronic submission of regulatory dossiers, ensuring compliance with various submission types such as 510(k), PMA, and IVDR Utilize platforms like Veeva Vault and eCTD Xpress to compile and validate regulatory submission packages Oversee submission lifecycle management and collaborate with cross-functional teams to troubleshoot publishing challenges Required Qualifications Bachelor's degree in Life Sciences, Regulatory Science, Quality Assurance, or a related field; advanced degree preferred 5+ years of experience in regulatory submission publishing within diagnostics or related life sciences industries Familiarity with AI, RPA, or regulatory publishing automation tools is highly preferred Strong understanding of FDA, EMA, and ICH regulatory standards Experience in continuous improvement and process automation
$85k
Title: Regulatory Affairs Associate Reporting to: Regulatory Affairs Manager Location: Boston, Massachusetts, USA We are seeking a highly motivated and results-driven Regulatory Affairs Associate to join our dynamic sales team at Venus AI. You are responsible for supporting...SuggestedFull timeWork at officeLocal areaRemote work$40 - $45 per hour
...Akkodis is seeking a Regulatory Affairs Associate for a Contract with a client in Santa Clara, CA. The ideal candidate will develop and manage regulatory-compliant medical device labeling, including IFUs, product labels, and country-specific addendums while coordinating...SuggestedHourly payContract workTemporary workWork at officeLocal area- ...Regulatory Affairs Associate Location: NC-RTP, US Contract Type: Regular Full-Time Area: OPERATIONAL TECHNICAL AREA Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people?...SuggestedFull timeContract workWork at office
- ...Job Title: Regulatory Affairs Associate Location: South Portland, ME - 100% Onsite Pay Range: $21/hr on W2 Job Details: Assist in the development and submission of product registration documentation Coordinate and prepare regulatory submission packages...SuggestedWeekly payTemporary workFlexible hours
$35 - $40 per hour
...Title: Regulatory Affairs Associate Location: Alameda, California (100% Onsite) Duration: 8+ months Shift Time: 8am to 5pm Pay Range : $35/hr to $40/hr (On W2) We are looking for a "Regulatory Affairs Associate" to join one of our Fortune 500 clients...SuggestedWork experience placementWork at officeShift work- ...Job Description Role: Regulatory Affairs Associate \n Location: Skaneateles Falls, NY(Hybrid) \n Duration: Long Term \n \n Required Education \n -Bachelor's degree or country equivalent in a scientific, engineering, regulatory, or related discipline \...
$65k - $97.5k
...on completion. Policy Management Prepare, update, and maintain HTA corporate policies, using interviews and meetings with associates and leadership. Support corporate policies at the other HTNA companies. Maintain HTA corporate policies library and dashboard...Full timeTemporary workWork experience placementInternshipRelocation package- ...pharmaceutical labeling • Preferred: Technical competency in labeling • Required: BS degree (or 3 years of equivalent experience in Regulatory Affairs) Additional Information Regards, _________________________________________________________________________ Pooja Mishra |...Work at office
- Role Support regulatory activities for Eton's pharmaceutical products, focusing on labeling, submissions, and compliance. Responsibilities... ...with cross-functional teams such as Marketing, Medical Affairs, QA, R&D, and Legal to ensure regulatory adherence. Maintain organized...
- Prepares device regulatory strategies that enable first pass approvals under limited management supervision. Develops and manages content... .... Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development...
- Role: Regulatory Affairs Associate Location: United States Duration: Long Term contract Position Summary We are seeking a detail-oriented Regulatory Affairs Associate to support regulatory activities for medical devices, pharmaceuticals, biotechnology products, or combination...Long term contract
$40 - $43 per hour
Job Title: Regulatory Affairs Operations SpecialistJob Description Responsibilities Design, develop, and implement international addendum... ...and up-to-date records of labeling changes, approvals, and associated documentation. Track labeling change requests across multiple...Contract workTemporary workWork at officeMonday to Friday- ...Europe and Asia enables us to be a powerful contributor and connector of right Talent. Job Description Description: The Regulatory Affairs Associate, with minimal guidance prepares, reviews and submits high quality annual reports with FDA within Annual report timelines...
- Efficient Auditing is seeking a Regulatory Affairs Associate to support regulatory submissions, compliance documentation, and product lifecycle management for clients across pharma, medical devices, biotech, and food industries. The role involves monitoring global regulatory...
- We are seeking a detail-oriented Regulatory Affairs Associate to support regulatory submissions, compliance documentation, and product lifecycle management for clients across pharmaceuticals, medical devices, biotech, and food industries. The ideal candidate will assist...Worldwide
- ...competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge. Job Description: The Regulatory Affairs Assistant supports efforts to ensure regulatory submission targets are met. Completes all duties under the direction of the...Work at office
- Job Title: Regulatory Affairs Associate Duration: 5 months Location: North Chicago, IL - Hybrid - (Tues - Thurs onsite); 60064 Description: Responsible for managing and compiling CMC sections of marketed product variations. Partner with RA CMC Project Leads and develop...Shift work
- ...quality systems or cross-functional project management Preferred Experience 6 years pharmaceutical experience including 5 years in regulatory affairs or 5 years in Discovery, R&D, or Manufacturing Experience working in a complex and matrix environment Strong oral and written...For contractors
- ...Regulatory Affairs Associate Doral, FL 33122 Overview Level Entry Position Type Full Time Education Level 4 Year Degree Category Other Description Position Type: Full Time Education Level: 4 Year Degree Category: Health Care / Regulatory & Clinical Support...Full timeWork at office
$28 - $30 per hour
Akkodis is seeking a Regulatory Affairs Specialist for a 12 Months contract position with a client located in Scarborough, ME. Ability to Work... ...and procedures. Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term...Hourly payContract workTemporary workLocal areaWork from homeWorldwide- Onsite in Plainsboro, NJ preferred (open to remote). Summary Our client has engaged GForce Life Sciences to provide a Regulatory Affairs Labeling Operations Specialist (Contractor) to support final printed pharmaceutical labeling for launch and lifecycle management initiatives...For contractorsRemote work
- Stark Pharma is looking for a detail-oriented Regulatory Affairs Associate to support regulatory activities for medical devices and pharmaceuticals. You will prepare and submit regulatory documentation, maintain compliance, and assist with FDA submissions to ensure adherence...
- ...Licensing and Regulatory Affairs Associate At MAJORITY, we're building a world where ambition knows no borders and where financial success follows you wherever life takes you. We've built a mobile banking platform for ambitious global citizens navigating life across...Work at office
- ...Maintains awareness of and utilizes current best practices for use of regulatory business systems within the group. Authoring and submitting... ...pharmaceutical experience including 1-2 years in regulatory affairs, R&D, or Manufacturing (CTD Module 3) May require an advanced...Shift work
- ...goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development... ...®. About the Role We are seeking a Senior Regulatory Affairs Associate, Regulatory Intelligence to join our team in a remote capacity...Full timeWork experience placementWork at officeRemote workWorldwideFlexible hours
- ...Job Description Job Description Summary: The Manager, Process Excellence within Regulatory Affairs is responsible for managing key process excellence and issue management activities that support compliant, efficient, and inspection-ready Regulatory Affairs operations...
- ...for the coordination and preparation of document packages for regulatory submissions ensuring compliance with the Food and Drug Administration... ...to other departments. Participates in assigned Regulatory Affairs initiatives aimed at improving internal Idenix standards and...Work at office
$30 - $36 per hour
...Job Description Job Description Job Title: Regulatory Affairs Associate I Position Type: Contract (12+ Months) Location: Clark, NJ 07066 Salary Rate: $30–36/hour Job Description We are seeking a detail-oriented Regulatory Affairs Associate I to support...Contract workWork experience placement$5,662.27 - $9,342.75 per month
...Job Description This position is the first line for providing answers to the field for all types of regulatory questions relating to TETRAC. Liaison with field offices around the globe to resolve governmental inquiries and issues including non-US customs, Food safety...Contract workWork at officeRemote workDay shift$30 - $33.65 per hour
Job Title: Roving Compliance Specialist Location: Irvine, CA 92612 Salary Range: $30.00 - $33.65 Hourly Position Type: Full Time Description Overview Travel to properties throughout portfolio within California as Roving Compliance Specialist...Hourly payFull timeWork at officeMonday to Friday
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