Pharma Labeling Graphic Designer (GMP/Regulatory)
Sanofi EU
Sanofi is seeking a Graphic Designer in Morristown, NJ to develop pharmaceutical product labeling artwork in accordance with U.S. and Canada regulations. You will ensure accuracy using regulatory text, layouts, and graphics, tracking projects to completion while meeting tight deadlines and maintaining high quality deliverables. Reports to GDPU PSA, Artork and ePI; the role supports artwork transformation, file management, and cross-site print production needs, with opportunities to contribute to #J-18808-Ljbffr Sanofi EU
- Eacademy Sanofi is seeking a Graphic Designer in Morristown, NJ, to develop pharmaceutical product labeling artwork in compliance with regulations. Ideal candidates will have a Bachelor's degree in graphic design and over 3 years of experience in pharmaceutical packaging...Suggested
- ...Job Title: Graphic Designer Grade: L2-2 Hiring Manager: Lisa Moher Location... ...pharmaceutical product labeling artwork in accordance with government... ...product labeling, utilizing regulatory text, technical layouts (... ...drawings Knowledge of GMP regulations Maintain an electronic...RegulatoryWorldwide
- Bristol-Myers Squibb in Summit, NJ is seeking a Manager, Label Operations to oversee label management within the S12 Cell Therapy manufacturing... ...will lead the Label Operations team, ensuring compliance with regulatory standards and efficient label issuance processes. The ideal...Regulatory
- ...Initial Therapeutics, Inc. is seeking a Global Labeling Strategist in Morristown, NJ or Cambridge, MA. You will lead the global labeling strategy and ensure compliance with regulatory standards for assigned products. Your role involves collaboration with cross-functional...Regulatory
$103.56k - $125.5k
Bristol-Myers Squibb is hiring a Manager for Label Operations at their Summit facility. This... ...team, ensuring compliance with regulatory standards, and fostering a collaborative... ...Bachelor's Degree and relevant experience in GMP and Quality compliance. The job includes...RegulatoryNight shift$103.56k - $125.5k
...p.m.-4:30 a.m. Responsibilities Implement/manage site Label Operations at S12 Summit West (Summit, NJ) per BMS policies... ...lead label management and align with global/regional regulatory requirements. Develop/maintain a GMP-compliant clinical and commercial label issuance and...RegulatoryWork at officeShift workNight shift$225k - $305k
Leo Pharma Inc. is seeking a Sr. Director for US Advertising & Promotion, Regulatory Affairs in Madison, NJ. This pivotal role involves guiding the strategy and compliance of all promotional activities with a focus on operational excellence and impactful business outcomes...Regulatory$225k - $305k
LEO Pharma is looking for a leader in Madison, New Jersey, to shape the strategy and compliance for dermatology solutions across the... ...Advertising and Promotion team, ensuring that all activities adhere to regulatory compliance while aligning with business objectives. The ideal...Regulatory$103.56k - $125.5k
## Manager, Label OperationsSummit West - NJ - USFind out how well... ...developing and maintaining a GMP compliant clinical and commercial... ...to ensure patient safety, regulatory requirements and improve its effectiveness... .... Employees in remote-by-design or lab-based roles may be...RegulatoryHourly payFull timeTemporary workPart timeFor contractorsWork experience placementSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift workNight shift$120k - $150k
...Products) plays a critical role in ensuring the quality, safety, and regulatory compliance of sterile pharmaceutical products manufactured by... ...(CMOs/CDMOs) accountable Strong understanding of global GMP and regulatory requirements (FDA, EMA, ICH) Ability to manage multiple...RegulatoryFull timeWork at officeLocal area- ...coordinate cross-functional teams to design, implement, and execute... ..., translational medicine, regulatory affairs, biostatistics, drug... ...activities and planned LCM for labelling changes Assessment of the... ...clinical development (experience in pharma or academia) Have...Regulatory
$153.6k - $230.4k
...premises and regulation, another applicable GMP guidelines and internal DS policies,... ...industry best practices and will withstand regulatory inspections by regulatory authorities... ...drug product manufacturing, packaging and labelling operations, QC testing and release, and...RegulatoryContract work$226.28k - $377.13k
...activities to support patient needs and demand. The Head partners with Regulatory Affairs, Supply Chain, Tech Unit and global Quality leaders to... ...secondary packaging. Expert knowledge of manufacturing and GMP QA requirements for a specific technical area. Ability to...RegulatoryContract work$145k - $170k
...US This range is provided by Averitas Pharma. Your actual pay will be based on your... ...oversight and strategic management of a designated portfolio of External Suppliers and/or... ...of Good Manufacturing Practices (GMP) and regulatory requirements within the pharmaceutical...RegulatoryFull timeContract workWorldwide- ...and more exclusive features. Job Title :QA Label Specialist Location : Summit, NJ Hours/... ...Maintains knowledge of current GMPs and regulatory guidelines. Requirements Bachelors... ...Quality Assurance Manager-Data Integrity/GMP/CSV Manhattan, NY $58,700.00-$63,301.00 1...RegulatoryContract workAfternoon shift
- ...The Regulatory Affairs Sr. Associate is an experienced medical device regulatory professional... ...content, evaluates product and labeling changes, supports post-market and vigilance... ...Maintain and improve Technical Documentation/Design Dossiers, GSPR/Essential Requirements...RegulatoryWork at office
- ...of PLAIR activities, prior to new product launch Manage regulatory correspondence mainly to CDER, FDA, User fee staff, drug listing... ..., derived from regulatory correspondences. Support TA Labeling team, when required. Participate in decision making process...RegulatoryLocal area
- ...operational excellence in a dynamic environment. In this pivotal role, you will engage with internal teams and external partners to uphold regulatory standards and drive compliance initiatives. Your expertise in cGMP and related guidelines will be crucial as you conduct...Regulatory
- ...Head of Regulatory Affairs About the Company Respected provider of top-quality services... ..., particularly in the areas of labeling, claims, and formulation, and requires a... ...degree in a related field, and experience in pharma and/or dermatology environments is a plus...Regulatory
- ...different production stages meet established quality standards and regulatory requirements. The candidate should have a Bachelor's degree in... ...discipline or relevant experience, strong understanding of GMP and GLP, and at least one year of experience in the beauty or CPG...Regulatory
- ...supporting validation efforts for drug products. Ideal candidates will have over 7 years in the pharmaceutical sector, understanding regulatory compliance, and are expected to frequently collaborate across functional teams. The position includes travel requirements of up...RegulatoryContract work
- ...microbiology QC across development and commercial programs. You will partner with Development, Technical Operations, QA, and CMC Regulatory to manage method transfers, validations, and data oversight within timelines. Lead a high‑performing QC team, drive risk‑based improvements...Regulatory
- Workplace Designation: Depending upon location, this role will be hybrid... ...for providing strategic regulatory advice and oversight for all... ..., promotional, and labeling aspects of relevant US regulatory... ...regulatory experience in the biotech/pharma industry, or a Ph.D., MD,...RegulatoryLocal areaRemote work
- ...management and compliance. This role will involve supporting the execution of processes, managing vendors, and ensuring adherence to regulatory requirements. The ideal candidate will have a Bachelor's degree or higher in Pharmacy or a related field, along with significant...Regulatory
- ...Advanced Degree Experience in Medical and/or Regulatory Affairs Clinical Background Strong... ...review, disease/brand and launch planning, labeling changes, business reviews, etc.... ...preferred Clinical and/or minimal 3 years of Pharma industry or agency experience preferred...Regulatory
- This role is responsible for providing strategic regulatory leadership and oversight for U.S. regulatory activities across a clinical-stage... ...clinical, nonclinical, and commercial components such as labeling and promotional materials. This position will serve as the primary...Regulatory
- ...a breadth of hands-on project management experience in the Pharma/Biotech/Cell Therapy regulated environments, the CTDO Sr.PM... ...experience in CAR T / Cell Therapy or Biologics. Understanding of GMP and FDA regulatory requirements correlating to biologics. Bachelors/Masters...Regulatory
- Job title Global Regulatory Lead Location Morristown, NJ / Cambridge, MA About the Job As the Global Regulatory Lead on our Global Regulatory... ...Strategy (GRPS), Global Submission Strategy, and core product labeling in development as well as for life cycle management of...Regulatory
$85.4k - $158.6k
...requests, ensuring alignment with LDC Core design. Coordinate with cross‑functional teams... ...processes and ensure alignment with GxP and regulatory standards. Project & Stakeholder... ...Skills Desired Data Analytics and Digital gmp knowledge HSE Knowledge Inventory Management...RegulatoryLocal areaAfternoon shift$225k - $275k
Description Overview As Senior Director of Regulatory Affairs - Cluster (North America), you are accountable for in-market regulatory activation... ...regulatory governance is applied to submissions, claims, and labeling decisions Regional Vigilance Accountable for regulatory...RegulatoryWork at officeLocal areaRemote work2 days per week
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