Pharma Labeling Graphic Designer — GMP & Regulatory Expert
Sanofi
Sanofi is seeking a Graphic Designer to develop pharmaceutical product labeling artwork in Morristown, NJ. This role involves creating high-quality artwork while adhering to FDA labeling regulations and GMP standards. The ideal candidate will have a Bachelor’s degree in graphic design and at least 3 years of experience in a regulated environment. Strong knowledge of Adobe Suite Software is essential, along with the ability to manage multiple projects under strict deadlines. #J-18808-Ljbffr Sanofi
- 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
$108.5k - $201.5k
...technical and development projects designed to characterize gene therapy... ...methods such as TMT labeling and label‑free quantitation.... ...; apply scientific/technical/GMP and/or quality‑related expertise... ...and technical documents for regulatory filings. Actively contribute...RegulatoryRelocation package- ...maintaining and optimizing facility systems including HVAC and clean utilities. You will ensure compliance with GMP, FDA, and EMA standards and support regulatory inspections. The ideal candidate has a Bachelor’s degree in Engineering and a minimum of 5 years experience...Regulatory
- ...qualifying new facilities while maintaining equipment systems in a validated state. The ideal candidate will possess strong knowledge of regulatory standards and excellent communication skills to collaborate effectively with internal teams and external vendors. Join a dynamic...Regulatory
$108.5k - $201.5k
...manufacturing. As the Sterility Assurance Expert, you will provide handson technical... ...decisions, strengthens compliance with evolving regulatory expectations, and continuously improves... ...and microbial control programs Design, maintain, and improve sterility assurance...RegulatoryRelocation package$93.8k - $174.2k
...and laboratory instrumentation. Ensures efficient, timely GMP, HSE and regulatory compliant maintenance and calibration of systems and equipment... ...service provider oversight as local process Subject Matter Expert (SME). Continuously develops personal and professional...RegulatoryLocal area- ...will be involved in pharmacokinetic analyses, clinical study support, and cross-functional collaboration, ensuring compliance with regulatory expectations. This is an excellent opportunity to apply your training in an impactful setting. #J-18808-Ljbffr Melinta...RegulatoryRemote jobFlexible hours
- ...Morristown, NJ. The role involves leading a team to ensure that products adhere to the highest regulatory standards, focusing on Safety Data Sheets (SDS) and product labels. You'll partner with various teams, overseeing compliance with global regulations while implementing...Regulatory
- ...Global Regulatory Lead Estimate start date July 7th At LEO Pharma, our mission transcends the conventional. We're on an ambitious... ..., achievement of desired labeling, and effective regulatory agency... ...functional project teams Maintain expert knowledge on regulatory...RegulatoryWorldwide
- ...experience in SAP logistics, supporting operational excellence, process improvements, and system implementations while adhering to regulatory standards. The role includes coordination of SAP Release projects and liaison with cross-functional teams to ensure that SAP...Regulatory
- An established industry player is seeking a meticulous Quality Assurance Label Specialist to support critical document control operations. This role involves ensuring compliance with cGMP regulations and managing the issuance of production labels. You will work collaboratively...
- Sanofi is seeking a Senior Manager, Regulatory Affairs Advertising and Promotion to join their GRA Advertising and Promo Team. In this role, you will conduct independent reviews of advertising and promotional materials while developing regulatory strategies for product...RegulatoryFull time
$120k - $150k
...suppliers. This role involves leading quality assurance efforts, conducting audits, and collaborating with teams across Supply Chain and Regulatory Affairs. Candidates should have a Bachelor's in Life Sciences and at least five years of QA experience, specifically in third-...Regulatory- Job Title: QA CTO Label Specialist Location: Summit, NJ 07901 Job Duration: 12+ Months Shift... ...S-12 facility to ensure patient safety, regulatory requirements and improve its... ...Must have knowledge and experience with GMP, Quality, and compliance. Able to write...RegulatoryWork experience placementWork at officeShift workAfternoon shift
- ...cross-functional teams to design, implement, and... ...translational medicine, regulatory affairs, biostatistics... ...Serve as a medical expert and provide strategic... ...activities and planned LCM for labelling changes Assessment... ...(experience in pharma or academia) Have experience...Regulatory
$99k - $232k
...Conduct and Compliance Industry/Sector: Pharma and Life Sciences Time Type: Full... ...risk and compliance focus on maintaining regulatory compliance and managing risks for clients... ...global compliance program strategy and design Knowledge of compliance automation solutions...RegulatoryFull timeH1b- ...documenting business processes, and ensuring the successful adoption of automation solutions. The ideal candidate should have expertise in regulatory compliance, strong analytical and problem-solving skills, and the ability to work effectively in a team. This position promises a...Regulatory
- A strategic workforce solutions provider in Parsippany-Troy Hills is seeking a Regulatory Specialist. Responsible for ensuring product registration accuracy and supporting regulatory documentation processes. The ideal candidate will have at least 2 years of experience,...Regulatory
$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...RegulatoryFull timeWork at officeLocal area$148.5k - $214.5k
...Job title: Global Labeling Strategist ~ Location: Morristown, NJ / Cambridge, MA... ...Information, EU SmPC), ensuring alignment with regulatory requirements and Sanofi's product... ...development and uses their insights to design studies that reflect real-world needs....RegulatoryLocal area$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- ...exclusive features. Job Title :QA Label Specialist Location : Summit,... ...knowledge of current GMPs and regulatory guidelines. Requirements... ...Assurance Manager-Data Integrity/GMP/CSV Manhattan, NY $58,700.00-$... ...knowledge in a new way. Experts add insights directly into each...RegulatoryContract workAfternoon shift
$225k - $305k
LEO Pharma UK is seeking a Sr. Director for US Advertising & Promotion in Madison, NJ. The role involves shaping dermatology solutions... .... Candidates should have a Master’s degree and 8+ years in regulatory affairs. Base salary ranges from $225,000 to $305,000 plus potential...Regulatory- ...industry player is seeking a Specialist in MS&T Manufacturing Labeling Systems to contribute to packaging and labeling materials project... ...planning for label changes, ensuring compliance with regulatory standards, and collaborating across functional teams. The successful...Regulatory
- ...Head of Regulatory Affairs About the Company Respected provider of top-quality services... ...regulations, particularly in the areas of labeling, claims, and formulation, and requires a... ...in a related field, and experience in pharma and/or dermatology environments is a plus...Regulatory
- ...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
$23 - $28 per hour
...hands‑on aseptic filling experience and a strong understanding of GMP standards Key Responsibilities Operate, monitor, and... ...environments ~ Strong understanding of GMP compliance and regulatory standards ~ Comfortable working onsite in a controlled manufacturing...RegulatoryContract workDay shift$157.59k - $203.94k
...release, stability, expiry, labeling, and cold-chain constraints.... ...manufacturing disruptions. GMP, GxP & Inspection Readiness... ...change controls, deviations, and regulatory impact assessments. Ensure... ...knowledge of clinical study designs, blinding practices, global trials...RegulatoryFor contractorsLocal areaWorldwideShift work$115k - $145k
...of 5-7 years of experience, along with a BA/BS degree. Responsibilities include managing PMRC meetings, ensuring compliance with regulatory authorities, and effective cross-functional collaboration. The base salary ranges from $115,000 to $145,000 with additional benefits...Regulatory$215k - $240k
...the future of dermatology by driving regulatory strategy for LEO Pharma's most exciting early-stage... ...opportunities. ~ Maintain expert knowledge of US regulatory requirements... ...Authority interactions, filings, and labeling. ~ Expert on US regulatory...RegulatoryPermanent employmentContract workWork at officeLocal area
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