RA Specialist

Sandoz; Alabama; Hybrid; USD 94,000 - 174,000; Full time

Benefits offered by this job

Health insurance

Hybrid work policy

401(k) retirement savings

Paid time off

Job summary

Sandoz in Princeton, NJ seeks a Regulatory Specialist, Regulatory Affairs CMC, to prepare and manage regulatory submissions, DMFs, and FDA communications across lifecycle of generic products. You will partner with cross-functional teams to ensure compliance and timely filings.

This role requires coordinating with FDA, sustaining regulatory records, and prioritizing workloads in a hybrid environment with some US office-based work, up to 50% remote.

Qualifications

• Prepare, review, and maintain regulatory submissions per FDA regulations and procedures.
• Experience with DMF/ANDA submissions and FDA interactions.
• Ability to manage multiple regulatory projects with minimal supervision.

Responsibilities

• Independently reviews, prepares, and maintains regulatory submissions including ANDAs, amendments, and annual reports.
• Prepare, submit, and maintain Type II and Type V DMFs and related documents.
• Collaborate with cross-functional teams to ensure regulatory compliance and timely submissions.
• Review labeling change control requests and approve revised labeling documents.

Skills

Regulatory submissions

Organization & execution

Agency & stakeholder communication

Analytical thinking & problem solving

CMC technical expertise

Education

Bachelor’s degree in a scientific related field

Tools

DMF filings

ANDAs

Job description

Job Description Summary

The Regulatory Specialist, Regulatory Affairs CMC, is responsible for preparing, submitting and maintaining regulatory submissions and Drug Master Files (DMFs) to support generic pharmaceutical products throughout their lifecycle. This role partners with cross-functional teams to support submission activities, regulatory assessments, and compliance with FDA regulations and company procedures.

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!

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.

Must be authorized to work in the U.S. U.S. work visa sponsorship is not available for this role now or in the future.

Major Accountabilities / Your Key Responsibilities:

• Independently reviews, prepares, and maintains regulatory submissions including ANDAs, amendments, supplements, annual reports, and responses to FDA deficiencies.

• Prepares, submits, and maintains Type II and Type V DMFs, amendments, annual reports, letters of authorization and responses to FDA deficiencies.

• Prioritizes workload. Receives little supervision for most assignments. Receives general instructions for non-standard analyses and projects.

• Collaborates with functional business units and external partners to ensure regulatory compliance and timely submissions.

• Reviews Labeling Change Control requests and approves revised labeling documents, which may include physician and patient package inserts as well as various types of container labels.

• Interacts with FDA regarding submissions.

• Performs regulatory assessments of change controls.

• Maintains regulatory records, databases, and document management systems in accordance with company procedures.

Key Performance Indicators:

• On-time submission of assigned regulatory filings

• Timely closure of regulatory commitments and FDA requests

• Compliance with regulatory requirements

• Timely assessment and closure of change controls

• High quality submissions with minimal FDA Deficiencies

Key Capabilities Required:

• Regulatory Submission: Ability to prepare, review, and maintain regulatory submissions in accordance with FDA regulations and company procedures.

• Organization & execution: Ability to prioritize workload, manage multiple projects simultaneously, and meet regulatory deadlines with minimal supervision.

• Agency & Stakeholder communication: Effectively manages communications with FDA, external partners, and functional business units.

• Analytical Thinking & Problem Solving: Ability to identify regulatory issues, evaluate information, and recommend solutions

• CMC Technical Expertise: Strong understanding of pharmaceutical manufacturing processes.

What you’ll bring to the role:

Required Qualifications:

Education & Experience (Required):

• Essential Qualifications

• Bachelor’s degree in a scientific related field

• 3-5 years Pharmaceutical Regulatory Affairs

• Problem solving skills

• Ability to manage multiple projects and regulatory deadlines simultaneously

• Experience working effectively in cross-functional teams

• Strong communication skills

• Good judgement and leadership ability

• Essential skills, Demonstrated ability to independently manage regulatory submissions and collaborate effectively across functional areas

Preferred Requirements:

• Advanced degree (MS, Pharm D, or equivalent) in a scientific discipline.

• Experience with ANDA and DMF filings

Travel Requirements:

Travel not required

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 - $174,200 USD/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 4.15.24[16].pdf

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 [e-mail] 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.

Salary Range

$93,800.00 - $174,200.00

Skills Desired

Analytical Skill, Clinical Trials, Collaboration, Detail-Oriented, Lifesciences, Project Planning, Regulatory Compliance