Are you a business? Hire fda regulatory candidates in Jersey City, NJ
Fork & Good is developing new approaches to growing meat without livestock. Our approach addresses critical food safety issues, cuts out the immense resources needed for livestock, and avoids animal slaughter. We are using innovative cell culture technologies to grow cells for products that have ...
Job Title: CSV (Computer System Validation) Specialist Location: Jersey City, NJ Job Summary: We are seeking an experienced Computer System Validation (CSV) Specialist with expertise in Valgenesis to join our team in Jersey City, NJ. The ideal candidate will have 7 to 10 years of experience in ...
Ensure all copy is scientifically accurate, compliant with regulatory guidelines (e.g., FDA, AMA), and adheres to brand style guidelines. * Present creative work to clients and internal stakeholders ...
Base understanding of data/regulatory processes (e.g., clinical trial phases, FDA approvals) * Ability to handle multiple tasks simultaneously and meet tight and sometimes conflicting deadlines
FDA & Healthcare Regulatory Firm Summary White & Case is an elite global law firm serving leading companies, financial institutions and governments worldwide. Our long history as an international ...
Following trial protocols in accordance with FDA regulations and ICH/GCP Guidelines. * Provide medical expertise to address study-related questions and ensure participant safety. * Collaborate with ...
FDA and FTC Regulatory Compliance: Maintain a thorough understanding of FDA and FTC regulations related to social media and influencer marketing in the healthcare industry. Ensure all activities are ...
Regulatory Knowledge : Comprehensive understanding of global beauty regulations, including FDA, EU, and Ulta/Sephora clean beauty standards. This job is primarily remote, however New York or Los ...
Regulatory & Compliance Oversight: Ensure adherence to industry-specific regulations (e.g., SEC, FDA, GDPR, HIPAA). * Team Leadership: Lead and mentor the legal department, including Assistant ...
... FDA, NIH, and all other applicable regulatory agency requirements. Responsibilities: Position responsibilities include, but are not limited to the following: Prepare all medications (research and ...
Develop, implement, and maintain the pharmaceutical quality management system (QMS) to ensure compliance with regulatory requirements (e.g., FDA, EMA), industry standards (e.g., cGMP), and company ...
Knowledge of FDA and OIG requirements, as well as the PhRMA Code, including regulations governing compliant scientific exchange * Ability to travel 60-70%, locally Work Environment: * Corporate ...
Proficient in managing third-party testing, with a solid understanding of regulatory requirements, including GMP, FDA, and other relevant guidelines. * Excellent analytical and problem-solving skills ...
... assure regulatory compliance within the culinary operations. · Provide technical support and ... updates of FDA food recalls. *NOTE: Essential functions, as defined under the Americans with ...
Advanced knowledge of regulatory and safety policies and procedures. * Proficient mathematical ... Exposure to FDA approved cleaning chemicals. * Exposure to temperatures: 90 degrees Fahrenheit
Internal regulatory entities * FDA guidelines/processes * Understanding of pharmaceutical/healthcare marketing best practices/requirements * Experience engaging with internal or external media teams ...
Identify, vet, and manage relationships with patient and healthcare provider (HCP) influencers, negotiating contracts and ensuring compliance with FDA and FTC regulations. * Content Development ...
Draft and review sophisticated contracts, ensuring compliance with FDA and other regulatory requirements. About the Firm Our client is a globally recognized law firm renowned for its expertise in ...
Ensure Top-Tier Standards - Maintain compliance with FDA/USDA food safety regulations. What You Bring * Creative Vision - Passion for contemporary, exciting, and innovative menu development
If and when applicable, maintains appropriate records of supplies and investigational drugs in protocol studies as required by government, hospital and FDA regulations. Assists clinician in writing ...
