1,124 regulatory manager jobs at 464 companies in Bethlehem, PA
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Senior Regulatory Compliance Manager
San Francisco or Salt Lake City or Phoenix or Los Angeles or Chicago or Boston or Austin or New York City or Miami or Tampa or Atlanta or Columbus or Boise or San Diego or Minneapolis or Houston or Raleigh or Nashville or Kansas City or Charlotte or Portland or Philadelphia or Dallas or Washington or Seattle
$173k-$223k/yrRemoteFull Time
CircleNYSE: CRCL: Digital currency issuer and blockchain financial infrastructure provider.
10+ YOERequires 10+ years in financial institution compliance or regulatory work, compliance program implementation, regulatory change management, regulatory analysis, cross-functional leadership, and familiarity with Slack, Apple MacOS, and GSuite.
Palm Beach Gardens or West Chester or Raynham or Oberdorf or Zuchwil
$117k-$201k/yrHybridFull Time
Johnson & JohnsonNYSE: JNJ: Provides pharmaceutical products and medical technology healthcare solutions.
6+ YOEBachelor's degree,6 years related experience in medical devices,knowledge of US/EU device regulations,RAC preferred,ability to manage regulatory submissions and teams,travel up to 10%.
Johnson & JohnsonNYSE: JNJ: Develops and manufactures pharmaceutical drugs and medical devices.
6+ YOEBachelor's degree or equivalent,6+ years regulatory experience in medical devices,knowledge of US/EU regulations,RAC preferred,ability to lead teams and interact with regulatory agencies,travel up to 10%.
Breckenridge Pharmaceutical: Develops and markets generic medicines in the United States.
8+ YOE8+ years regulatory affairs experience with ANDA submissions for sterile injectables, bachelor’s in pharmacy/chemistry/biology required, B.S. required; advanced degree/MBA preferred, strong written/oral communication and regulatory CMC expertise.
PPLNYSE: PPL: Provides electricity and natural gas to millions of customers.
10+ YOE10+ years energy industry experience with regulatory, rate, procurement and financial expertise; Bachelor's degree required; MBA/master's preferred; strong decision-making and leadership skills.
West Pharmaceutical ServicesNYSE: WST: Manufactures packaging and delivery systems for injectable medicines.
8+ YOEBachelor's degree with 8+ years or master's/PhD with 3+ years in regulated healthcare technologies; expertise in medical device software, cybersecurity, regulatory strategy, submissions, and digital health.
IEC 62304, IEC 82304, ISO 14971, Title 21 CFR, EU MDR 2017/745
California or Los Angeles or Los Angeles County or San Francisco or Philadelphia or United States
$113k-$154k/yrOnsiteFull Time
Victoria's Secret & Co.NYSE: VSCO: Retailer of lingerie, apparel, and beauty products.
5+ YOEBachelor's degree in a relevant field and 5–7+ years regulatory affairs experience in cosmetics/personal care; strong knowledge of global cosmetic and packaging regulations; experience with global launches and submissions; cross-functional influence and mentoring skills.
Jefferson: Providing healthcare services and academic programs in Pennsylvania.
5+ YOEBachelor’s degree and 5 years of product development, regulatory implementation, or project management experience, preferably in healthcare; expertise in complex projects, cross-functional work, systems integration, migration, and testing.
Church & DwightNYSE: CHD: Produces household and personal care consumer goods and chemicals.
8+ YOEBachelor's degree, 8+ years regulatory affairs experience in cosmetics, experience with NPD and lifecycle change control, regulatory master files and dossiers, project management, and strong communication skills.
Church & DwightNYSE: CHD: Manufacturer of household and personal care consumer products.
8+ YOEBachelor's degree and 8+ years of cosmetic regulatory affairs experience required, including global regulations, NPD launch readiness, lifecycle change control, regulatory dossiers, project management, and cross-functional leadership.
Colgate-PalmoliveNYSE: CL: Manufactures and sells oral, personal, home, and pet care.
7+ YOEBachelor's in life sciences/quality/regulatory required; 7+ years in regulatory/compliance (2+ years project management); strong knowledge of ISO 13485, ISO 14971, FDA 21 CFR 820; eQMS/DMS and Smartsheet proficiency.
Smartsheet, GreenlightGuru, electronic Quality Management Systems (eQMS), document management systems (DMS)
Otsuka PharmaceuticalTokyo Stock Exchange: 4578: Develops and manufactures innovative pharmaceutical and nutritional products.
7+ YOEMinimum 7 years regulatory operations experience with eCTD submissions, knowledge of FDA/EMA/Swiss Medic guidance, Documentum and publishing tools, Microsoft Office/SharePoint proficiency, staff supervision and vendor coordination.
Documentum, DocuBridge, InSight Publisher, GlobalSubmit Validate, GlobalSubmit Review, ISIToolbox, eCTD, Microsoft Word, Microsoft Excel, Microsoft Access, Microsoft PowerPoint, Microsoft SharePoint
Opella: Develops and manufactures consumer healthcare and self-care products.
5+ YOEBachelor's degree and 5–8 years of regulatory affairs experience required, including 4+ years supporting OTC NDA drugs and knowledge of U.S. regulatory submissions, labeling, and product lifecycle management.
HaleonLondon Stock Exchange, New York Stock Exchange: HLN: Global leader in consumer healthcare and over-the-counter medicines.
7+ YOEBachelor's in pharmaceutical/life sciences required, 7+ years regulatory affairs experience (FDA/OTC/CMC), proven leadership, FDA interaction experience, strong communication and project management skills.
Los Angeles or Atlanta or Cincinnati or Milwaukee or New York or Minneapolis or Chicago or Boston or Philadelphia or Denver or Charlotte
$139k-$164k/yrHybridFull Time
U.S. BankNYSE: USB: Provider of personal, business, and institutional financial services.
8+ YOELaw degree and license to practice in jurisdiction, 8+ years related experience, knowledge of the Investment Company Act of 1940, ability to manage teams and complex projects, strong communication and regulatory drafting skills.
InsmedNasdaq: INSM: Global biopharmaceutical developing therapies for serious, rare diseases.
5+ YOEBachelor's degree and 5+ years regulatory affairs experience in pharma/biotech; experience preparing IND/CTA, NDA/BLA, MAA and regulatory submissions; Veeva Vault and MS Office proficiency; strong organization and communication skills.
Veeva Vault, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Adobe Acrobat, SmartSheet
RegeneronNasdaq: REGN: Discovers and manufactures medicines for serious diseases.
2+ YOEDoctorate (MD/PhD/PharmD) and 2+ years regulatory experience; experience with INDs/CTAs, agency interactions, filings, and knowledge of US FDA and international regulations.
Regeneron PharmaceuticalsNASDAQ: REGN: Discovers and develops medicines for serious diseases.
2+ YOEDoctorate (MD/PhD/PharmD) and 2+ years regulatory experience; knowledge of US FDA and international guidance; experience with filings, agency interactions, and CRO engagement preferred.
CSLASX: CSL: Develops and manufactures biopharmaceutical products and vaccines.
5+ YOEBachelor's degree in a relevant life science, 5+ years of biotech or pharmaceutical regulatory experience, 3+ years with developmental products, regional regulatory knowledge, and health authority interaction experience.
3+ YOEBachelor's degree in a pharmaceutical-related field required; 3–5 years of biotech or pharmaceutical regulatory experience preferred, including FDA submissions, eCTD, submission planning, Veeva RIM, and ePublishing.
eCTD, Regulatory Information Management Systems (RIMS), Veeva RIM