Recordati Group
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Regulatory Affairs Manager
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Recordati Rare Diseases North America Join to apply for the
Regulatory Affairs Manager
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Recordati Rare Diseases North America Get AI-powered advice on this job and more exclusive features. Direct message the job poster from Recordati Rare Diseases North America With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn. We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries. At Recordati, our mantra is simple. Weve always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Whether that is for common diseases or the rarest we want to give people the opportunity to be the best version of themselves. This drive will never stop. Together, we will always be reimagining tomorrow with new ideas, new technologies and new innovations to fight diseases. Recordati. Unlocking the full potential of life. This position is with Recordati Rare Diseases, Inc. (RRD), North America, an affiliate of Recordati. Recordati Rare Diseases, Inc. (RRD) develops high-impact therapies for rare diseases, focusing on providing treatments to underserved communities in the U.S. Our mission is to mitigate the impact of rare diseases through increased awareness, better diagnoses, and improved treatment access in endocrinology, metabolic, hematology and oncology franchises. RRD is dedicated to fostering a dynamic work environment that promotes professional growth and a significant impact on patients' lives. Reporting Structure Reports To: Senior Director, Regulatory Affairs, Strategy and Lifecycle Management Direct Reports: N/A Areas Managed: Regulatory Affairs Overview Manage RRD Regulatory Affairs for assigned products for US and Canada, including implementation of the overall regulatory strategy, preparation of regulatory submissions and interface with relevant health authorities. Implement regulatory strategies supporting drug development and lifecycle management for US and Canada. Review documentation and prepare lifecycle management submissions. Review documentation and prepare drug development activity of pre-IND and IND submissions. Liaise with regulatory authorities as needed pertaining to drug development and product lifecycle management. Oversee submission of advertising and promotional material to the FDA as required. Support the labeling and/or change control processes to ensure timely and comprehensive review. Maintain labels/labeling for newly acquired and existing products in compliance with regulatory requirements and company standards. Track Annual Report and Periodic Safety Update Reports (PSUR) schedules to ensure that required dossiers are prepared and submitted as required. Coordinate with Medical Affairs & Pharmacovigilance to ensure timely reporting of safety data to regulatory agencies and partners. Ensure compliance with all federal regulations regarding post-marketing reporting to the FDA and other health authorities. Act in full compliance with all laws, regulations, and policies including adverse events / pharmacovigilance responsibilities. Perform additional duties as may be assigned. Education And Experience Bachelors degree required; advanced degree in the life sciences preferred. A minimum of 5 years experience in Regulatory Affairs Experience in a commercial-stage organization required. Demonstrated ability to deliver quality results within a fast-paced, dynamic environment. Knowledge And Skills Knowledge of current FDA and Health Canada regulations and guidance; and knowledge of and experience with pharmacovigilance and related drug safety reporting regulations. Ability to manage multiple priorities and regulatory submissions at different stages as required. Strong project management skills with proven ability to drive projects through to completion. Working knowledge of Veeva platform helpful but not required. This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. Based upon job requirements, employee may be required at times to attend meetings including travel out of state over weekends and nights. Employee must be able to freely operate and travel by car and train/plane modes of transportation. Employee is required to have a valid drivers license and means of transportation. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be able to fly via commercial air carrier. This is largely a sedentary role; however, the employee frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms; talk and hear. Occasionally is required to lift and/or move light to moderate weight up to 25 lbs. Location/Travel This position is located at RRDs US headquarters in New Jersey. Approximately 10% travel (domestic and international) required. FLSA Classification This position is considered Exempt. EEO Statement It is the policy of Recordati Rare Diseases to provide equal employment opportunity (EEO) to all persons regardless of race, color, religion, sex, sexual orientation, gender identity, or national origin. Further, Recordati Rare Diseases will not discriminate based on any characteristic protected by federal, state, or local law. Recordati Rare Diseases will provide reasonable accommodation for qualified individuals with disabilities. Disclaimer This job description is not designed to cover or contain a comprehensive listing of the activities, duties or responsibilities that may be required. Disclosures Pay Range (Base Pay): $108,000 - $148,500. Other Types of Pay: annual bonus Health Insurance: Medical, dental, orthodontia, vision, life & ADD, short and long term disability insurance benefits. Paid Time Off: Vacation, holiday, and sick/personal time At Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential. We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief. If you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today. Seniority level
Seniority level
Mid-Senior level Employment type
Employment type
Full-time Job function
Job function
Legal and Other Industries
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Regulatory Affairs Manager
role at
Recordati Rare Diseases North America Join to apply for the
Regulatory Affairs Manager
role at
Recordati Rare Diseases North America Get AI-powered advice on this job and more exclusive features. Direct message the job poster from Recordati Rare Diseases North America With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn. We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries. At Recordati, our mantra is simple. Weve always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Whether that is for common diseases or the rarest we want to give people the opportunity to be the best version of themselves. This drive will never stop. Together, we will always be reimagining tomorrow with new ideas, new technologies and new innovations to fight diseases. Recordati. Unlocking the full potential of life. This position is with Recordati Rare Diseases, Inc. (RRD), North America, an affiliate of Recordati. Recordati Rare Diseases, Inc. (RRD) develops high-impact therapies for rare diseases, focusing on providing treatments to underserved communities in the U.S. Our mission is to mitigate the impact of rare diseases through increased awareness, better diagnoses, and improved treatment access in endocrinology, metabolic, hematology and oncology franchises. RRD is dedicated to fostering a dynamic work environment that promotes professional growth and a significant impact on patients' lives. Reporting Structure Reports To: Senior Director, Regulatory Affairs, Strategy and Lifecycle Management Direct Reports: N/A Areas Managed: Regulatory Affairs Overview Manage RRD Regulatory Affairs for assigned products for US and Canada, including implementation of the overall regulatory strategy, preparation of regulatory submissions and interface with relevant health authorities. Implement regulatory strategies supporting drug development and lifecycle management for US and Canada. Review documentation and prepare lifecycle management submissions. Review documentation and prepare drug development activity of pre-IND and IND submissions. Liaise with regulatory authorities as needed pertaining to drug development and product lifecycle management. Oversee submission of advertising and promotional material to the FDA as required. Support the labeling and/or change control processes to ensure timely and comprehensive review. Maintain labels/labeling for newly acquired and existing products in compliance with regulatory requirements and company standards. Track Annual Report and Periodic Safety Update Reports (PSUR) schedules to ensure that required dossiers are prepared and submitted as required. Coordinate with Medical Affairs & Pharmacovigilance to ensure timely reporting of safety data to regulatory agencies and partners. Ensure compliance with all federal regulations regarding post-marketing reporting to the FDA and other health authorities. Act in full compliance with all laws, regulations, and policies including adverse events / pharmacovigilance responsibilities. Perform additional duties as may be assigned. Education And Experience Bachelors degree required; advanced degree in the life sciences preferred. A minimum of 5 years experience in Regulatory Affairs Experience in a commercial-stage organization required. Demonstrated ability to deliver quality results within a fast-paced, dynamic environment. Knowledge And Skills Knowledge of current FDA and Health Canada regulations and guidance; and knowledge of and experience with pharmacovigilance and related drug safety reporting regulations. Ability to manage multiple priorities and regulatory submissions at different stages as required. Strong project management skills with proven ability to drive projects through to completion. Working knowledge of Veeva platform helpful but not required. This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. Based upon job requirements, employee may be required at times to attend meetings including travel out of state over weekends and nights. Employee must be able to freely operate and travel by car and train/plane modes of transportation. Employee is required to have a valid drivers license and means of transportation. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be able to fly via commercial air carrier. This is largely a sedentary role; however, the employee frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms; talk and hear. Occasionally is required to lift and/or move light to moderate weight up to 25 lbs. Location/Travel This position is located at RRDs US headquarters in New Jersey. Approximately 10% travel (domestic and international) required. FLSA Classification This position is considered Exempt. EEO Statement It is the policy of Recordati Rare Diseases to provide equal employment opportunity (EEO) to all persons regardless of race, color, religion, sex, sexual orientation, gender identity, or national origin. Further, Recordati Rare Diseases will not discriminate based on any characteristic protected by federal, state, or local law. Recordati Rare Diseases will provide reasonable accommodation for qualified individuals with disabilities. Disclaimer This job description is not designed to cover or contain a comprehensive listing of the activities, duties or responsibilities that may be required. Disclosures Pay Range (Base Pay): $108,000 - $148,500. Other Types of Pay: annual bonus Health Insurance: Medical, dental, orthodontia, vision, life & ADD, short and long term disability insurance benefits. Paid Time Off: Vacation, holiday, and sick/personal time At Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential. We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief. If you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today. Seniority level
Seniority level
Mid-Senior level Employment type
Employment type
Full-time Job function
Job function
Legal and Other Industries
Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Recordati Rare Diseases North America by 2x Get notified about new Regulatory Affairs Manager jobs in
Bridgewater, NJ . Associate Director, Regulatory Affairs - Labeling Management
Rahway, NJ $126,500.00-$199,100.00 3 days ago Manager, Regulatory Operations Documentation Specialist - Contractor
Florham Park, NJ $65.00-$85.00 1 month ago Livingston, NJ $102,400.00-$204,100.00 1 week ago Senior Scientist/Associate Director, Regulatory Affairs CMC
Morristown, NJ $140,000.00-$180,000.00 2 weeks ago Senior Manager, Global Regulatory Affairs Labeling
Princeton, NJ $170,000.00-$192,000.00 6 days ago Associate Director of Regulatory Affairs
East Hanover, NJ $120,000.00-$160,000.00 1 week ago Senior Scientist/Associate Director, Regulatory Affairs CMC
Associate Director, Global Regulatory Affairs, Strategy
Princeton, NJ $165,600.00-$248,400.00 6 days ago Counsel - Corporate Contracts Regulatory Affairs
Senior Manager Regulatory Affairs, Advertising and Promotion - Job ID: 1690
Princeton, NJ $170,000.00-$185,000.00 2 weeks ago Senior Manager, CMC Regulatory Affairs Small Molecules
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Clark, NJ $126,900.00-$184,000.00 1 week ago Vice President, Global Regulatory Affairs
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Regulatory Affairs Regional Associate Director, LACan
East Hanover, NJ $132,300.00-$245,700.00 2 weeks ago Associate Director, Global Regulatory Affairs Global Labeling Strategy
Morristown, NJ $147,000.00-$212,333.33 1 week ago Piscataway, NJ $170,000.00-$200,000.00 1 week ago Madison, NJ $115,000.00-$140,000.00 13 hours ago Associate Director Regulatory Affairs CMC
Princeton, NJ $160,000.00-$199,600.00 1 day ago Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr