Talent.com
Senior Regulatory Affairs Consultant - Labeling (European Expertise)
Senior Regulatory Affairs Consultant - Labeling (European Expertise)Atlanta Staffing • Atlanta, GA, US
Senior Regulatory Affairs Consultant - Labeling (European Expertise)

Senior Regulatory Affairs Consultant - Labeling (European Expertise)

Atlanta Staffing • Atlanta, GA, US
6 days ago
Job type
  • Full-time
Job description

Senior / Consultant, Regulatory Labeling

Incredible, high-impact role with a Global Biopharma sponsor! Are you ready to turn your labeling expertise into strategic impact? We're seeking a sharp, detail-driven Senior / Consultant, Regulatory Labeling to join a dedicated partnership with a leading global biopharmaceutical company. In this high-visibility role, you'll be more than a consultant you'll be a trusted collaborator whose insights help shape regulatory strategy and ensure patients worldwide receive safe, effective therapies with clarity and confidence.

In this role, you'll be the go-to expert for global labeling, working side-by-side with client teams across Regulatory Affairs, Technical Operations, Safety, and Commercial. You'll help navigate the complex regulatory landscape, ensure compliance across international markets, and drive continuous improvement in how labeling is developed, tracked, and delivered.

As a Senior / Consultant, Regulatory Labeling, you will partner with Label Strategist to :

  • Conduct international labeling operations activities to support global new product and supplemental applications to product registration, and post approval launches for impacted international markets.
  • Collaborate with Technical Operations team members to ensure commercial distribution, Regulatory Technology for labeling submissions, PV for safety reporting, and other functional groups. Provide labeling to Advertising and Promotion for marketing pieces, and with Commercial for website postings if needed.
  • Work with Regulatory Operations, Regulatory Affairs, Tech Ops, etc. for labeling distribution, tracking and quality control.
  • Utilize regulatory / product knowledge to provide operational support to ensure that labeling materials meet regulatory and company requirements and timelines.

You will also :

  • Be responsible for executing and effective quality control reviews and tracking (primarily) internally used labeling documents (Core Data Sheet, Core Patient Information Leaflet, Core Instructions for Use) and outward facing local / regional labeling (USPI, Med Guide, SmPC, PIL, Canadian Product Monograph, Instructions for Use) as well as container and carton labels to meet regional regulatory requirements and ensure consistency between labeling, labels and supportive documents.
  • Act as operational expert for Global Labeling tracking in RIMs, SPL generation, ensure development and maintenance of templates, collaboration features and system upgrades.
  • Contribute to the continuous improvement of the end-to-end labeling process including excellent proofreading / editing skills and compiling supportive documentation.
  • Support labeling inspection / audit readiness activities.
  • Demonstrates the use of the organization's consulting models and methodologies and uses experience to suggest possible developments / improvements.
  • Business Development :

  • Maintain and continue to grow a network of industry colleagues through relationships formed during project engagements or through other industry experience.
  • Actively participates in project scoping calls and proposal preparation.
  • May deliver sales presentations and participate in bid defense meetings when needed.
  • Contributes information to support the account planning process and integrated marketing programs.
  • Contributes ideas for approaches to new clients or new service offerings.
  • Parexel-related Responsibilities :

  • Meets established metrics as specified in scorecard on an annual basis.
  • Completes basic job-related responsibilities, including timesheets, expense reports, maintenance of CVs, project deliverable archiving, participation in internal initiatives / projects or as a mentor as requested by management.
  • Defines self-development activities to keep current within the industry (i.e. maintain membership in a relevant industry and / or scientific / technical association).
  • May participate in thought leadership activities (i.e. present speeches or seminars to industry groups and / or author articles.)
  • Skills :

  • Strong attention to detail.
  • Solid understanding and interpretation of EU / US labeling regulatory requirements.
  • Solid understanding of requirements for tracking of labeling updates.
  • Solid understanding of the pharmaceutical industry drug development process and willingness to learn global labeling regulatory requirements and industry practice.
  • Solid aptitude for use of IT systems; Regulatory Information Management System (RIMS), electronic document management system (EDMS), Proficiency in MS Office suite; Willing to learn additional applications.
  • Understanding of label development and submission processes preferred.
  • Ability to recognize and escalate issues.
  • Strong written and oral communication and organizational skills.
  • Ability to generate and initiate problem solving innovative solutions.
  • The ideal candidate should be action-oriented, customer focused, ability to manage workloads and set priorities. In addition, he / she should be capable of dealing with ambiguity, be creative, and be comfortable working with multifunctional teams.
  • High-level consulting skills.
  • Critical thinking and problem-solving skills.
  • Knowledge and Experience :

  • Good working knowledge of key labeling regulations / guidance and past experience in label development (CCDS, USPI, packaging).
  • Strong experience with EU labeling regulations is essential and US labeling experience is highly desired.
  • The ability to research and create comparator labeling documents.
  • Strong understanding and past experience creating annual reports.
  • The ability to collaborate with Tech Ops for artwork implementation.
  • Proficiency in SPL (all aspects, types and troubleshooting) and the ability to manage the review and approval of labeling in a document management system.
  • Electronic document management systems use and / or electronic submission experience.
  • Extensive years of experience in an industry-related environment; experience with a regulatory agency (such as FDA, MHRA) is a plus.
  • Education :

  • Bachelor's Degree plus at least 4+ years of experience in drug development especially in labeling, product package coordination, clinical supplies / packaging, supply chain regulatory affairs, or quality.
  • Exceptional candidates with 3+ years of labeling related experience may also be considered.
  • If you thrive in fast-paced, high-stakes environments and love the idea of being a key player in a global regulatory role - apply today!

    Create a job alert for this search

    Senior Consultant • Atlanta, GA, US

    Related jobs
    Regulatory Compliance Specialist

    Regulatory Compliance Specialist

    Horizon Asset Group • Cartersville, GA, US
    Full-time
    Quick Apply
    Regulatory Compliance Specialist Location : .Cartersville, GA (On-site) Company : Superior Medical Supply About Us : Superior Medical Supply is a growing provider of high-quality Durable Medical ...Show more
    Last updated: 30+ days ago
    Travel CT Technologist

    Travel CT Technologist

    LRS Healthcare - Allied • Lithonia, GA, US
    Permanent
    LRS Healthcare - Allied is seeking a travel CT Technologist for a travel job in Lithonia, Georgia.Job Description & Requirements. LRS Healthcare - Allied Job ID #30I-99746.Pay package is based o...Show more
    Last updated: 5 hours ago • Promoted • New!
    Regulatory Affairs Specialist

    Regulatory Affairs Specialist

    AmerisourceBergen Corporation (Cencora) • Atlanta, GA, United States
    Full-time
    Our team members are at the heart of everything we do.At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on ...Show more
    Last updated: 30+ days ago • Promoted
    Regulatory Change Analyst : 25-07031

    Regulatory Change Analyst : 25-07031

    Akraya • Atlanta, GA, US
    Full-time
    Primary Skills : Regulatory Compliance (Expert), Audits (Advanced), Risk Management (Advanced), Legal Frameworks (Advanced), Change Management (Expert). Job Summary : We are seeking a Regulatory Compl...Show more
    Last updated: 2 days ago • Promoted
    Regulatory Analyst Sr - Remote

    Regulatory Analyst Sr - Remote

    Georgia Staffing • Atlanta, GA, US
    Remote
    Full-time
    Regulatory Analyst Sr - Remote.At Prime Therapeutics (Prime), we are a different kind of PBM, with a purpose beyond profits and a unique ability to connect care for those we serve.Looking for a pur...Show more
    Last updated: 14 hours ago • Promoted • New!
    Travel CT Tech - $2,006 to $2,306 per week in Lithonia, GA

    Travel CT Tech - $2,006 to $2,306 per week in Lithonia, GA

    AlliedTravelCareers • Lithonia, GA, US
    Full-time
    AlliedTravelCareers is working with Fusion Medical Staffing to find a qualified CT Tech in Lithonia, Georgia, 30058!.Fusion Medical Staffing is seeking a skilled CT Tech for a 13-week travel assign...Show more
    Last updated: 3 days ago • Promoted
    Remote Editorial Specialist

    Remote Editorial Specialist

    Outlier • Lawrenceville, GA, United States
    Remote
    Full-time
    Earn up to $15 / hour + performance bonuses.Outlier, a platform owned and operated by Scale AI, is looking for.If you're passionate about improving models and excited by the future of AI, this is you...Show more
    Last updated: 7 days ago • Promoted
    Experienced Chemical Regulatory Specialist (Remote) Part time

    Experienced Chemical Regulatory Specialist (Remote) Part time

    Pace Analytical Services, LLC • Norcross, GA, United States
    Remote
    Full-time +1
    Monday through Friday, 8 : 00AM - 5 : 00PM less than 20 hours per week.Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovat...Show more
    Last updated: 11 days ago • Promoted
    Plan Review Consultant

    Plan Review Consultant

    FM • LAWRENCEVILLE, Georgia, United States
    Full-time
    FM is a leading property insurer of the world's largest businesses, providing more than one-third of FORTUNE 1000- size companies with engineering-based risk management and property insurance solut...Show more
    Last updated: 8 days ago • Promoted
    Compliance Analyst - Regulatory

    Compliance Analyst - Regulatory

    LocumTenens.com • Alpharetta, GA, United States
    Full-time
    The Compliance Analyst - Regulatory will be responsible for providing specialized support to the Legal team in the area of statutory and regulatory requirements impacting the locum tenens industry....Show more
    Last updated: 30+ days ago • Promoted
    Travel CT Technologist

    Travel CT Technologist

    American Traveler • Lithonia, GA, US
    Full-time
    American Traveler is seeking a travel CT Technologist for a travel job in Lithonia, Georgia.Job Description & Requirements. American Traveler is seeking a CT Technologist with at least 18 months...Show more
    Last updated: 3 days ago • Promoted
    Regulatory Affairs Specialist

    Regulatory Affairs Specialist

    CorDx • Alpharetta, GA, US
    Full-time
    Quick Apply
    CorDx, a multi-national biotech organization, focused on pushing the limits of innovation and supply in global health.With over 2000 employees across the world serving millions of users in over 100...Show more
    Last updated: 7 days ago
    Senior Manager, Regulatory Affairs & Quality Assurance, APAC

    Senior Manager, Regulatory Affairs & Quality Assurance, APAC

    Avanos Medical • Alpharetta, GA, United States
    Full-time
    Job Title : Senior Manager, Regulatory Affairs & Quality Assurance, APAC.Here at Avanos Medical, we passionately believe in three things : . Making a difference in our products, services and offers, nev...Show more
    Last updated: 23 hours ago • Promoted
    Travel Multimodal Technologist

    Travel Multimodal Technologist

    Junxion Med Staffing • Fayetteville, GA, US
    Permanent
    Junxion Med Staffing is seeking a travel Multimodal Technologist for a travel job in Fayetteville, Georgia.Job Description & Requirements. Junxion Med Staffing Job ID #1347515.Pay package is bas...Show more
    Last updated: 5 hours ago • Promoted • New!
    Regulatory Affairs Manager

    Regulatory Affairs Manager

    Katalyst Healthcares & Life Sciences • Atlanta, GA, US
    Full-time
    Responsibilities : In this critical role, you will lead regulatory strategies, product submissions, and a team of talented regulatory affairs professionals to drive timely product approvals and ensu...Show more
    Last updated: 30+ days ago • Promoted
    Specialist, Regulatory Affairs

    Specialist, Regulatory Affairs

    AmerisourceBergen Corporation (Cencora) • Atlanta, GA, United States
    Full-time
    Our team members are at the heart of everything we do.At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on ...Show more
    Last updated: 30+ days ago • Promoted
    Travel Interventional Radiology Technologist

    Travel Interventional Radiology Technologist

    Uniti Med • Austell, GA, US
    Full-time
    Uniti Med is seeking a travel Interventional Radiology Technologist for a travel job in Austell, Georgia.Job Description & Requirements. Interventional Radiology Technologist.Cigna medical, MetL...Show more
    Last updated: 30+ days ago • Promoted
    Senior Principal Medical Writer - Regulatory - Oncology - Single Sponsor

    Senior Principal Medical Writer - Regulatory - Oncology - Single Sponsor

    Syneos Health / inVentiv Health Commercial LLC • Atlanta, GA, United States
    Full-time
    Senior Principal Medical Writer - Regulatory - Oncology - Single Sponsor.Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.We...Show more
    Last updated: 21 days ago • Promoted