## [Regulatory Contract Staffing Services](/regulatory-contract-staffing-services) # Regulatory Contract Staffing Services In today’s dynamic Regulatory landscape, the **biggest challenge** for the Life Sciences industry is **finding a skilled and qualified workforce** on time. At the time of process improvements, integration of new technologies, or implementation of a new process/tool to comply with the evolving regulations, the scenario becomes even more crucial as it demands timely addressal of resource gaps. ![ Regulatory Contract Staffing Services]() With over 10+ years of aggregated experience in life sciences, Freyr brings in the pragmatic inputs while evaluating and assessing the Regulatory staffing requirements for **Pharmaceutical (Generics, New Drugs), Biologics (Innovators and Biosimilars), Medical Devices, Cosmetics, Food and Food Supplements, Chemicals, etc.** Freyr has a track record of supporting **Global pharma companies** meet their demanding staffing requirements on time. Learn more about Freyr’s proven expertise here. Freyr is specialized in catering Regulatory workforce for the following functionalities and industry segments: ## Functionality-wise Designations ## ![]() Regulatory Affairs CMC - Regulatory CMC Author - Regulatory CMC Expert - Regulatory CMC Manager - Regulatory Strategist - Regulatory Senior Strategist - CMC Specialist - CMC Information Management Market Authorization Applications - Regulatory Project Manager - Regulatory Affairs specialist – NDA, IND, CTA, IMPD, ANDA, BLA, PMA/510K, Global MAH - Regulatory Lifecycle and Global Dossier Coordinator / Dossier Compilation Project Coordinator - Dossier Preparation Specialist More ## ![]() Regulatory Medical Writing, PDE Medical Writing Staffing Roles - Medical Writer - Content Specialist - Regulatory Medical Writer - Senior Medical Writer - Quality Reviewer - Medical Reviewer - Clinical Expert - Clinical Lead - Clinical Trial Monitoring Specialist - QC Expert - QC Specialist - Nonclinical Expert - Nonclinical Writer - Toxicologist PDE - Nonclinical Expert/Senior Nonclinical Writer - Toxicologist - Safety Assessor More ## ![]() Regulatory Information Management - XEVMPD Specialist - IDMP Solution Specialist More ## ![]() Regulatory Labeling - Global/ Regional Labeling Coordinator - Global Labeling Lead - Regulatory Strategist - Labeling Manager - Labeling Expert/Specialist - Senior Labeling Specialist - Labeling Program Manager - Labeling Project Manager - Regulatory Labeling Associate - Core Data Sheet (CDS) Manager - CDS Development Lead - Label Content Experts / Medical Writers and Authors - Core Data Sheet (CDS), Summary of Product Characteristics (SmPC), Package Insert (PI), Patient Information Leaflet (PIL), Regional Labels - CDS / Regional Label Content and Process Coordinator - Global Labeling Project / Program Manager - Label Content – Quality Control (QC) Specialist More ## ![]() Compliance, Audit & Validation Compliance and Validation - Head - Lead - Business Process Specialist - Senior Associate - Associate - GCP/GMP/GxP Auditor - QMS Remediation Expert - GxP Solution Consultant Compliance and Audit - Assistant manager - Business Process Specialist - Business Process Analyst - Senior Associate Validation - Business Process Specialist - Business Process Analyst - Senior Associate - Associate More ## ![]() Publishing and Submissions - Publishing and Submission Specialist - Senior Publisher - ISI Toolbox Specialist More ## ![]() Pharmacovigilance Pharmacovigilance - Safety Associate - Safety Expert - Pharmacovigilance Expert - Pharmacovigilance Scientist - Safety Lead - Literature Monitor - Aggregate Report Writer - Aggregate Report Specialist - Quality Reviewer - Medical Reviewer - Signal Evaluation Specialist - Signal Evaluation Expert - Safety Data Specialist - Safety Data Lead More ## Segment-wise Designations ## ![]() Consumer, Cosmetics & Food Supplements - Regulatory Specialist - Senior Regulatory specialist - Junior Regulatory specialist - Coordinators - Subject Matter Expert/Solutioning Lead - Global Project Manager /Program Manager - Label Content and QC Specialist - Label Content Expert - Regulatory Document Translator - Local Support Expert - Legal Representative/License Holding - Local Language Expert - Responsible Person - Content Management Expert - Administrative Support Associate - Client Call Expert - Claims Consulting Expert - Regulatory Strategist More ## ![]() Medical Devices - Device Labeling Specialist - Labeling Manager - Label Content – QC Specialist - Regulatory Affairs Associate - Senior Regulatory Affairs Associate - Assistance Manager Regulatory Affairs - Regulatory Affairs Manager - Regulatory Affairs Project Manager - Regulatory Affairs Strategist - EU - Medical Device Regulation (MDR) Specialist - Regulatory Affairs Lead - Post Market Surveillance - Clinical Evaluation Report (CER) Specialist - Performance Evaluation Report (PER)/Scientific Validation Report Specialist - Literature Search Associates/Managers - 510(k) Specialist/US Submission Specialist - PMA Specialist - Device History File Specialist - Device Labeling Reviewer - CE Marking Specialist/EU Submission Specialist More We hope the designations mentioned above suit your strategic objectives. Kindly give us a few more details for any specific requirement. We assure to find a tailored fit. [Let Us Source](javascript:void(0)) ###   ## Preferred Staffing Vendor With a top-notch recruiting team backed by 2300+ qualified and high-performing Regulatory professionals, Freyr supports customers in choosing the right talent at the right time. Freyr offers Regulatory contract staffing services across the **USA, Canada, South America, Europe, the UK, Middle East, Africa, and Asia**. As a proven partner for Regulatory staffing (project-based, short-term, and/or long-term), we aim to make your staffing journey streamlined and cost-effective. Also, we would love to prove our capabilities to become your preferred staffing vendor. [**Drop us a URL**](javascript:void(0)) **where we can fill the details and get an opportunity to talk to you.**