Associate Director, Global Regulatory Labeling
Artech Information Systems LLC
Company DescriptionArtech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• Flex position in Global Labeling, for a Global Labeling Product Leader for the Infectious Diseases/Vaccines/Global Public Health Therapeutic Area. The GLPL will have responsibility for: • The creation and maintenance of primary and derived labeling documents, and text for artwork for packaging components through the LWG and LC processes, as required • Ensuring quality of primary and derived labeling documents, and text for artwork for packaging components (e.g., alignment of labeling text with data, regulatory requirements, consistency (where appropriate) between labeling documents) • Contribution to and implementation of the global labeling strategy including the development of target labeling • Principal responsibilities include: • The creation and maintenance of primary (Core Company Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, EU Product Information (EUPI)) and derived (International Package Insert, labeling text for EU, US and international package components, and translations) labeling documents. Takes into account competitor labels when drafting labeling text. • Coordinates the development, revision, review and approval of primary and derived labeling documents including the Labeling working Group (LWG) and Labeling Committee (LC) activities related to these documents • Ensures dissemination of LC-approved CCDS, USPI, EUPI and derived labeling documents and supporting documentation • Ensures quality of labeling deliverables (e.g., alignment of labeling text with data, regulatory requirements, consistency (where appropriate) between labeling documents) • Contributes to and implements the global labeling strategy.Additional InformationSneha ShrivastavaTechnical Recruiter (Clinical/Scientific)Artech Information Systems LLC360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: View phone number on job-api.jobget.com | Fax: 973.998.2599Connect with us on - LinkedIn | Facebook | TwitterSummaryType: ContractFunction: ResearchExperience level: ExecutiveIndustry: Pharmaceuticals
- ...cost.Job Description• Flex position in Global Labeling, for a Global Labeling Product Leader... ...alignment of labeling text with data, regulatory requirements, consistency (where appropriate... ...States Package Insert (USPI) and associated patient labeling, EU Product...SuggestedWork at officeImmediate startFlexible hours
- Role: Associate Director, Global Labeling Product Leader within Johnson & Johnson's Innovative Medicine R&D, responsible for developing and executing... ...with cross-functional teams (clinical, safety, regulatory, commercial), and aligning labeling strategies with global...SuggestedLocal areaWorldwide
$137k - $235.75k
...their merit.Job Function: Regulatory Affairs GroupJob Sub Function... ...for the best talent for an Associate Director, Regulatory Affairs, North... ...responsible for North American and global regulatory strategies for... ...lead the development of NA labelling negotiation strategies, and...SuggestedFull timeLocal areaImmediate startFlexible hours$142.4k - $224.1k
...building a leading portfolio to improve and save lives of people with Lung, Head & Neck and Gastrointestinal (GI) cancers. The Associate Director Global Solid Tumors will play a vital role in building and maximizing the Global opportunity for these solid tumor franchises and...SuggestedFull timeFor contractorsLocal areaFlexible hours$173.2k - $272.6k
Job DescriptionRole Summary:The Global Associate Director Medical Affairs (GADMA) has scientific and working knowledge in their area of responsibility (eg, defined tumor, asset, vaccine) and responsible for supporting execution of the Global Medical and Scientific Affairs...SuggestedFull timeFor contractorsLocal areaFlexible hours$142.4k - $224.1k
...DescriptionThe newly formed Integrated Global Respiratory Business Unit is advancing... ...strategic, scientifically curious Associate Director, Enterprise Brand Strategy to help shape... ...partnership with Medical Affairs, Clinical, Regulatory, and Regional teams.Develop the...Full timeFor contractorsLocal areaFlexible hours- Role Summary Global Associate Director Medical Affairs (GADMA) supports execution of the Global Medical & Scientific Affairs (GMSA) portion for assigned Therapeutic Areas (TA) in alignment with Global Value & Implementation (V&I) Plans. Focus on US with support for Rest...
- Role Associate Director, Transcend R&D BPO Logistics & Global Trade, overseeing end-to-end logistics and global trade processes within R&D operations. Responsibilities define, govern, and evolve future-state process roadmaps; translate R&D strategies into capability plans...
- Location: North Wales, Pennsylvania, United StatesCompany: MerckPosted: 2026-09-14Merck is seeking a Global Associate Director Medical Affairs (GADMA) to lead scientific initiatives across defined therapeutic areas and support global Medical and Scientific Affairs execution...
$142.4k - $224.1k
...This is a pivotal moment to join the Global Infectious Diseases Team as a prescription... ...Infectious Diseases portfolio. As an Associate Director on the Global Commercial Team, you... ...across Marketing, Medical, Market Access, Regulatory, Supply, and other key functions....Temporary workFor contractorsLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift work- Role Associate Director, Enterprise Brand Strategy within the Global Respiratory Business Unit, focusing on shaping HCP engagement strategies and scientific narratives... ...-functional teams (Medical Affairs, Clinical, Regulatory) on congress planning, advisory boards, and KOL...Local area
- ...planning, budget administration, and personnel management of the Global Knowledge Management (GKM) team. This role will contribute... ...connections to access, share, and apply relevant scientific, regulatory, and industry information that supports organizational goals....Contract workShift work
- Scorpion Therapeutics seeks a senior candidate to lead AI-enabled regulatory CMC initiatives in a fast-paced biotech environment. You will drive AI drafting, digital tooling adoption, and cross-functional collaboration to modernize regulatory submissions. You will mentor...
$166.5k - $203.5k
...therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious... ...the right way.Reporting to the Senior Director, Global Pharmacovigilance Compliance, Standards... ...functional leaders (e.g., Clinical Operations, Regulatory Affairs, Quality Assurance, and the...Minimum wageFull timeWork at officeLocal areaFlexible hours- Scorpion Therapeutics seeks an Associate Director, Transcend R&D BPO Logistics & Global Trade to oversee end-to-end logistics and global trade processes within R&D operations, ensuring alignment with strategy and compliance. You will define future-state roadmaps, translate...
- Makro Scientific is seeking a Hub Labeling Manager in Collegeville, Pennsylvania, with 3-5 years of experience and preferred pharmaceutical... ...local product documents and ensuring compliance with regulatory standards. The ideal candidate will communicate effectively, prioritize...Local area
$137k - $235.75k
...Medicine R&D is recruiting for an Associate Director, Signal Detection Scientist.... ...safety data, international regulatory safety databases, and other... ...preferred.Understanding of global health authority regulations... ...event dictionaries; core labeling; Periodic Safety Review preparation...Full timeImmediate start- Our Company is seeking a Global Associate Director Medical Affairs (GADMA) to lead scientific execution in assigned Therapeutic Areas with a strong cross-functional and global orientation. The role emphasizes executional excellence, strategic agility, and partner engagement...
- ...Job Title: Director, Regulatory Affairs, Pharmaceuticals Employment Type: Permanent Location... ...About ClinChoice ClinChoice is a global full-service CRO dedicated to... ...lifecycle, including Development, CMC, Labeling, Promotion, Commercialization, and Operations...Permanent employment
- CSL seeks an Associate Director, Global Knowledge Management to shape and lead our enterprise‑wide knowledge strategy across biotechnology and... ...scientific and operational insights. Partnering with R&D, medical, regulatory, and commercial functions, you will drive adoption of KM...Worldwide
- ...the Upper Merion site. You will drive 0-12 week schedules, improve run rate, and ensure GMP/FDA compliance while coordinating with Global Planning on longer horizons. You will lead the S&L team, monitor CtS performance, and partner with cross-functional stakeholders to...
$142.4k - $224.1k
Job DescriptionThe Global Clinical Supply (GCS) organization is responsible for managing... ...trials. GCS oversees the sourcing, labeling, packaging, and global distribution of clinical... ...Good Distribution Practices (GDP) and regulatory requirements.Experience with SAP or...Full timeContract workFor contractorsLocal areaWorldwideFlexible hoursShift work$231.9k - $365k
Job DescriptionOur Regulatory Affairs team in General Medicine advances... ...enabled by engagement with global health authorities. We work across... ...Description:The Executive Director, Regulatory Affairs Liaison... ...time to approval and optimize labeling.Provide oversight for direct...Full timeFor contractorsLocal areaWorldwideFlexible hours- Medasource is seeking a Regulatory Program Manager to drive global regulatory strategy into executable plans, coordinating cross-functional teams to ensure timely submissions and compliant deliverables. The RPM will partner with the GRL and external partners to accelerate...Contract workImmediate start
$129k - $203.1k
...welfare of animals; comply with applicable global regulatory requirements through sound processes... ...contractor-initiated investigations associated with deviations, negotiation of site... ...following areas: Clinical Packaging and Labelling, Distribution of clinical supplies...For contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$137k - $235.75k
...are searching for the best talent for a Associate Director, Thought Leader Liaison, Hematology... ...-functional action plans to address on-label issues as needed to ensure flawless customer... ...Partner Enablement, Developing Others, Global Market, Inclusive Leadership,...Contract workTemporary workWork experience placementWork at officeLocal areaImmediate startRemote workShift work- A global biopharmaceutical company seeks an Associate Director, Launch Strategy & Operations. In this pivotal role, you will shape integrated launch plans, ensuring strategic alignment and operational excellence across functions. Ideal candidates will have a Bachelor's...
- ...Scorpion Therapeutics is seeking a Senior Scientist Product Lead in CMC Regulatory Affairs, focusing on synthetics and new modalities. You will drive global regulatory strategies and dossier development for innovative medicines in a senior capacity. The role emphasizes...
$137k - $235.75k
...& Johnson Innovative Medicine (IM) is recruiting for an Associate Director of AI Quality and Governance - R&D Data Science & Digital... ...leader will partner closely with DSDH teams, Quality, Legal, Global Regulatory Affairs, and Johnson & Johnson Technology (JJT) to streamline...Full timeLocal areaImmediate start$156.9k - $247k
...operational outcomes.Position SummaryThe Associate Director, Advanced Process Analytics & Data... ...analytics, root-cause investigations, and regulatory-ready manufacturing data products.Key... ...practices and tools across a complex, globally distributed organization.Ability to...Full timeContract workFor contractorsLocal areaFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Associate Director, Global Regulatory Labeling. Be the first to apply!
- associate manager Spring House, PA
- associate director Spring House, PA
- regulatory cmc Spring House, PA
- clinical research regulatory Spring House, PA
- regulatory Spring House, PA
- regulatory contract Spring House, PA
- regulatory scientist Spring House, PA
- regulatory law Spring House, PA
- associate program manager
- associate campaign manager



