Regulatory Affairs Compliance Sr. Specialist Job at Sandoz, Princeton, NJ

Y1ZDQnZvRHU3TDl0NHNQQW9ENkEwV1k9
  • Sandoz
  • Princeton, NJ

Job Description

Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally.

Join us, the future is ours to shape!

Drive best practices and operational excellence within the department and cross-functionally by providing key regulatory intelligence updates via knowledge sharing and training to advance US regulatory expertise within Sandoz.

Ensure compliance with internal procedures as the Regulatory Affairs point of contact for onboarding activities and global contact for training and reporting.

Position Location:

This position will be located at the Princeton, NJ US Headquarters site.

Our Sandoz flexible hybrid working approach allows US office-based employees to work up to 50% of their monthly workday remotely. This role will not have the ability to be located remotely. Preference will be given to local candidates not requiring relocation.

Major Accountabilities / Your Key Responsibilities:

Your responsibilities include, but not limited to:

  • Work with QA to author and maintain RA SOPs and Work Instructions
  • Work with QA to maintain and update the curriculums and training for individuals in RA
  • Work with the Associate Director of Compliance to manage onboarding for new employees in RA
  • Assist the Associate Director of Compliance with user fee related activities, CARES Act reporting, FDARA reporting and FDA registration and listing activities.
  • Prepare and submit License renewals
  • Monitor regulatory changes and assess their impact on existing and future products, advising stakeholders accordingly.
  • Responsible for addressing requests for CoPPs, FOIA information, Samples and Apostille documentation
  • Oversee the Annual Reports process and maintain the master schedule.
  • Manages regulatory projects within the regulatory group and with other departments, including creating and tracking deadlines and progressing projects

Key Capabilities Required:

  • Knowledge of relevant laws and regulations
  • Able to work independently and in a team environment
  • Excellent communication and interpersonal skills
  • Technical system skills (e.g. MS office applications, databases, efficient online research)

What you’ll bring to the role:

Required Qualifications:

Education:

  • BS in a scientific field

Experience:

  • 7+ years of professional related experience including a minimum of 5 years of regulatory experience

Preferred Requirements:

  • Generic experience

You’ll Receive:

Sandoz offers a generous employee benefits package that includes a competitive salary, health insurance coverage for medical, prescription drugs, dental and vision, a generous company match for retirement savings accounts, and generous paid time off. We also follow a hybrid work policy that combines a mix of in-person and remote work to allow our employees flexibility.

The pay range for this position at commencement of employment is expected to be between $93,800 – 134,000 – 174,200 USD/year; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

On September 30, 2021, Sandoz entered into a 5-year Corporate Integrity Agreement. Certain positions will have responsibilities to support the execution and adherence to CIA obligations, CIA-related deliverables, and any relevant audit, monitoring or Independent Review Organization (IRO) remediation.

Why Sandoz?

Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more!

With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.

Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported!

Join us!

Sandoz EEO Statement:

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Sandoz Reasonable Accommodations Statement:

Sandoz, Inc. is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an email to reasonable.accommodations@sandoz.com or call 1-609-422-4098 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Join our Sandoz Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Sandoz and our career opportunities, join the Network here:

#Sandoz

Job Tags

Local area, Remote job, Relocation, Relocation bonus, Flexible hours,

Similar Jobs

TRC Talent Solutions

Office Administrator Job at TRC Talent Solutions

 ...About the Role: Were looking for an organized, detail-oriented Office Administrator to join a great team in Columbia, SC. This is a dynamic, multi-tasking role that involves handling office communications, onboarding new team members, supporting payroll and financial... 

Ultimate Staffing

Clinical Data Curator- Biology Degree required Job at Ultimate Staffing

 ...Clinical Data Curator (Biology Degree Required) - Temp-to-Hire Pay: $24/hour Schedule: Mon-Fri, 8:00AM-4:30PM Remote: Equipment provided Start date: Early June 2025 What You'll Do: Interpret and enter clinical data from test requisition forms and... 

C-SUITE ASSISTANTS

Personal Assistant Job at C-SUITE ASSISTANTS

 ...household staff to ensure smooth day-to-day operations. Organize and manage personal, domestic/international travel arrangements using private aircraft. Provide a broad range of administrative support, run errands, manage cars and insurance, plan dinners/events, make... 

The Northport Hotel

Restaurant Manager Job at The Northport Hotel

 ...You will also assume a variety of responsibilities and duties such as recruiting and hiring restaurant staff, training, overseeing food quality, creating and executing restaurant marketing strategies, developing menus, as well as greeting and serving restaurant guests... 

EPM Scientific

Regulatory Affairs Specialist Job at EPM Scientific

 ...Title: Regulatory Affairs Specialist Summary: A global leader in the ophthalmic medical device industry, is seeking an experienced and driven Regulatory Affairs Specialist to join their team in Pennsylvania. This position is perfect for a candidate with strong...