RA Manager

Job Description Summary

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.

Major Accountabilities / Your Key Responsibilities:

Your responsibilities include but not limited to:

• Participates in Global RA project meetings & provides input into global strategy for US submissions. Is responsible for implementing the agreed upon strategies for assigned projects

• Prepare US eCTD documents & facilitating timely submissions and approvals to support the biosimilar pipeline

• Management of high-quality regulatory documents and tracking of regulatory activities in relevant IT systems to support team deliverables. Maintain regulatory archive systems.

• Support local regulatory requirements such as preparation of NDC forms annual reports etc to ensure compliance with regulatory health authorities.

• Determines requirements and sets objectives for Health Authority (HA) interactions as applicable.

• Coordination of key regulatory information between various departments and participates in launch preparation activities.

• Execute and manage operational activities for assigned projects.

Key Performance Indicators:

• Successful implementation of regulatory strategy for timely submissions and approvals based on available data.

• Pro-active working style demonstrating leadership and embraces the Sandoz cultural principles

• Successful Participation in relevant regulatory teams meetings as well as cross functional meetings and providing valuable input on projects.

• Adherence to Sandoz policy and guidelines -Project & stakeholder feedback

Key Capabilities Required:

• Regulatory & compliance Expertise: Deep understanding of health authorities regulations and guidance documents associated with drug development labeling and post-marketing compliance with the ability to apply this knowledge to ensure seamless execution of submissions approvals and regulatory compliance activities

• Project & Portfolio Management Expertise:Strong organizational skills and attention to detail with the ability to support multiple regulatory projects simultaneously managing timelines priorities and deliverables across various stages of product development

• Communication and Interpersonal Skills:Strong verbal and written communication skills with the build professional relationships actively listen and communicate with clarity and confidence in a fast-paced team-oriented environment.

• Analytical and Problem-Solving Skills:Strong analytical thinking and a proactive approach to problem-solving with the ability to evaluate regulatory requirements troubleshoot issues risk mitigation and support decision-making processes with sound judgment and accuracy.

• Writing and Documentation Skills:Professional writing and documentation skills are essential ensuring all regulatory submissions and internal documentation meet quality consistency and compliance standards.

What youll bring to the role:

Required Qualifications:

Education & Experience (Required):

• Bachelor in a science required

• 3-5 years experience in regulatory affairs preferably in biosimilars area

• Industry Awareness: Knowledge of existing and upcoming industry trends and regulatory changes.

• Demonstrated understanding of relevant regulations and standards from highly regulated agencies such as theFDA EMA and MHRA

• Proficiency in data analysis and regulatory document preparation.

• Experience with HA meetings and communications

• Languages: Fluent English required (oral and written)

Preferred Requirements:

• Ability to work independently under pressure demonstrating initiative and flexibility.

• Team spirit and embracing diversity of cultures and personalities.

Travel Requirements: Up to 5%

Youll 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 $114100- 211900USD/year; however while salary ranges are effective from 1/1/26 through 12/31/26 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.

Sandoz - Notice at Collection to Employees Applicants

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!

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.

Accessibility and reasonable accommodations

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 in order to perform the essential functions of a position please send an email to or call 1- and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Salary Range

Skills Desired