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Biosimilar Jobs (NOW HIRING)

The individual will support the US Biosimilar Regulatory Affairs team and will work with various project teams on licensed products as well as products in development. The individual will be ...

The individual will support the US Biosimilar Regulatory Affairs team and will work with various project teams on licensed products as well as products in development. The individual will be ...

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Biosimilar information

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$61

How much do biosimilar jobs pay per hour?

As of Jul 24, 2026, the average hourly pay for biosimilar in the United States is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $30.77 per hour, depending on experience, location, and employer.

What are biosimilars?

Biosimilars are biological medicines that are highly similar to already approved reference biologic drugs, with no clinically meaningful differences in terms of safety, purity, or effectiveness. They are developed once the patent for the original biologic has expired, and undergo rigorous regulatory assessment to ensure their quality. Biosimilars are used to treat a range of diseases, such as cancer and autoimmune disorders, often at a lower cost than the original biologics. They help increase patient access to important therapies and encourage competition in the pharmaceutical market.

What is the difference between Biosimilar vs Pharmacist?

AspectBiosimilarPharmacist
Required CredentialsBiotechnology degree, specialized training in biologicsDoctor of Pharmacy (PharmD), licensure
Work EnvironmentPharmaceutical manufacturing, research labsCommunity pharmacies, hospitals, clinics
Industry UsageBiotech, pharmaceutical companiesHealthcare, retail, hospital settings
Common Search/ComparisonBiologics, biosimilar developmentMedication dispensing, patient counseling

While biosimilars are biologic products similar to original biologic drugs, pharmacists are healthcare professionals who dispense medications and advise patients. Both roles are integral to the pharmaceutical industry but differ in focus, credentials, and work environment.

What are some common challenges faced by professionals working in biosimilar development, and how can they be addressed?

Professionals in biosimilar development often encounter challenges such as navigating complex regulatory requirements, ensuring product comparability, and managing cross-functional collaboration between scientific, clinical, and regulatory teams. Staying updated with evolving guidelines from agencies like the FDA and EMA is crucial, as is fostering open communication across departments to streamline data sharing and decision-making. Proactively engaging in continuous professional development and leveraging cross-disciplinary expertise can help address these challenges and contribute to successful biosimilar product development.

What are the key skills and qualifications needed to thrive as a Biosimilar Scientist, and why are they important?

To thrive as a Biosimilar Scientist, you need a solid background in biochemistry, molecular biology, or related life sciences, often supported by advanced degrees like an MSc or PhD. Familiarity with analytical techniques (e.g., HPLC, mass spectrometry), regulatory guidelines (FDA, EMA), and quality control systems is essential. Strong problem-solving, teamwork, and communication skills help navigate complex development processes and cross-functional collaboration. These competencies ensure successful biosimilar development, regulatory approval, and product safety.
More about Biosimilar jobs
What states have the most Biosimilar jobs? States with the most job openings for Biosimilar jobs include:
Infographic showing various Biosimilar job openings in the United States as of July 2026, with employment types broken down into 97% Full Time, 1% Part Time, 1% Contract, and 1% Nights. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $54,791 per year, or $26.3 per hour.

U.S. Biosimilars Regulatory Lead -- Hybrid Work

U023 (FCRS = US023) Sandoz Inc

Princeton, NJ • On-site

$145.60 - $279.40/hr

Other

Posted 10 days ago


Job description

Sandoz Inc in Princeton, NJ, is looking for an Associate Director of Regulatory Affairs – Biosimilars to lead U.S. regulatory strategy for biosimilar development. This pivotal role involves overseeing regulatory submission processes and ensuring compliance with FDA regulations while collaborating cross-functionally for timely approvals.

The ideal candidate will have at least 7 years of experience in regulatory affairs with a strong focus on biosimilar programs, supported by a relevant academic background. The position offers a competitive salary along with a hybrid work environment.

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