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Manager Biosimilars Jobs (NOW HIRING)

Fresenius Kabi

Manager, Marketing

Lake Zurich, IL · On-site

$105K - $130K/yr

Job Summary The Manager, Marketing (Biopharma Provider Strategy) will actively contribute to the ... biosimilars portfolio, including personal and non-personal promotion, product theatres, etc.

Freseniusglobal

Manager, Marketing

Lake Zurich, IL · On-site

$105K - $130K/yr

Job Summary The Manager, Marketing (Biopharma Provider Strategy) will actively contribute to the ... biosimilars portfolio, including personal and non-personal promotion, product theatres, etc.

Lucyrx

Clinical Strategy Pharmacist

Bethesda, MD · On-site +1

$126K - $151K/yr

Ensure formulary strategies align with LucyRx's broader clinical programs, including biosimilars, specialty management, chronic disease, and value-based initiatives * Contribute to governance ...

Imedica

Manager, Clinical Pharmacy

Omaha, NE

The Manager, Clinical Pharmacy is responsible for leading the development, maintenance, and ... Lead pipeline assessment and drug readiness activities for new molecular entities, biosimilars ...

Medica

Manager, Pharmacy Clinical Governance

Omaha, NE · On-site

The Manager, Pharmacy Clinical Governance is responsible for leading the development, maintenance ... Lead pipeline assessment and drug readiness activities for new molecular entities, biosimilars ...

Imedica

Manager, Clinical Pharmacy

Minnetonka, MN

The Manager, Clinical Pharmacy is responsible for leading the development, maintenance, and ... Lead pipeline assessment and drug readiness activities for new molecular entities, biosimilars ...

Imedica

Manager, Clinical Pharmacy

Madison, WI

The Manager, Clinical Pharmacy is responsible for leading the development, maintenance, and ... Lead pipeline assessment and drug readiness activities for new molecular entities, biosimilars ...

Getinge

Territory Manager, Bioprocessing

New York, NY · On-site

... and biosimilars in the Pharmaceutical industry, as well as enzymes, food, feed, bio-fuel, bio ... Relay observed market trends and competitive intel to the management team. * Organize and execute ...

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All JobsManager Biosimilars Jobs

Manager Biosimilars information

See salary details

$28.5K

$62.7K

$113.5K

How much do manager biosimilars jobs pay per year?

As of Jul 4, 2026, the average yearly pay for manager biosimilars in the United States is $62,661.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,000.00 and $69,000.00 per year, depending on experience, location, and employer.

What is the difference between Manager Biosimilars vs Regulatory Affairs Manager?

AspectManager BiosimilarsRegulatory Affairs Manager
CredentialsBiotech/Pharma degree, industry certificationsRegulatory or life sciences degree, certifications like RAC
Work EnvironmentBiotech/Pharmaceutical companies, R&D labsRegulatory agencies, pharma companies, consulting firms
Industry UsageDeveloping biosimilar products, clinical trialsPreparing regulatory submissions, compliance
Search IntentRoles in biosimilar development, product managementRegulatory processes, approval procedures

The Manager Biosimilars focuses on overseeing the development and commercialization of biosimilar products, requiring expertise in biotech and product management. In contrast, the Regulatory Affairs Manager handles regulatory submissions and compliance, often with a background in regulatory affairs or life sciences. While both roles operate within the pharmaceutical industry, their core responsibilities and required credentials differ, making each role distinct in the drug development process.

How much does a biosimilar regional account manager make?

A biosimilar regional account manager typically earns between $90,000 and $130,000 annually, depending on experience, location, and company size. Compensation may also include bonuses and commissions based on sales performance, with strong communication and product knowledge being key skills for the role.

What biology jobs pay over $100k?

Manager Biosimilars is a specialized role in the biopharmaceutical industry that can pay over $100,000 annually, especially with experience and advanced degrees. Other high-paying biology-related jobs include pharmaceutical project managers, senior research scientists, and regulatory affairs directors, often requiring strong industry knowledge, certifications, and leadership skills.

What jobs in the US pay 300,000 a year?

In the US, high-paying roles related to Manager Biosimilars or similar fields often include senior executive positions such as Vice President or Director of Biosimilars, pharmaceutical executives, and specialized healthcare consultants. These roles typically require advanced degrees, extensive industry experience, and leadership skills, with salaries reaching or exceeding $300,000 annually. Compensation varies based on company size, location, and individual expertise.

What is the highest paying job in pharmaceuticals?

In the pharmaceutical industry, senior executive roles such as Chief Medical Officer, Vice President of Research and Development, or Vice President of Commercial Operations tend to be the highest paying. These positions require extensive experience, leadership skills, and often advanced degrees, and they oversee strategic decision-making and large teams within pharmaceutical companies.
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Manager Biosimilars jobs near you
Senior Scientist - Biosimilars ARD

Senior Scientist - Biosimilars ARD

Kashiv Biosciences LLC

Piscataway, NJ • On-site

$91K - $125K/yr

Full-time

Posted 18 days ago

Job description

Job Type
Full-time
Description
Summary
A Sr. Scientist I will be a key technical resource responsible for independently developing methods, generating reliable and interpreting data, using analytical instrument that include HPLC, UPLC, GC, UV/Vis, dissolution apparatus and particle analyzer. You will be expected to develop a close working relationship with technical personnel at all levels within the organization to provide technical support needed in meeting R&D milestones and goals.
Conduct instrumenttroubleshooting.or designing experiments, writing method validation protocols, conducting method validation, and processing and interpreting the analytical data.
Essential Duties & Responsibilities
  • Develop and validation analytical method for drug substances, drug products, and excipients
  • Conduct routine and advanced analytical tests in accordance with SOPs and regulatory guidance.
  • Write protocols, reports, methods, standard operation procedure, and submission documents.
  • Provide analytical support for formulation and process development.
  • Perform independent scheduling and coordination of activities
  • Complies with all companypolicies and standards
  • Analyze analytical data, identify trends and provide recommendation.
  • Review laboratory notebooks, raw data and technical documentation (e.g. test method, validation protocol, or validation report) in support of regulatory filings
  • Train and provide technical guidance to junior scientists.
  • Conduct laboratory investigation and prepare laboratory investigation report.
  • Proactively provide Lab management with suggestions on how to improve the methods, lab practice or lab system.
  • Evaluate and improve existing test methods
  • Proactively provide Lab management with suggestions on how to improve the methods, lab practice orlab system.ection.
  • Review and evaluate drug substance supplier's technical documents and provide recommendation in APIvendor selection.
  • Performs other functions asrequired or assigned

Requirements
PREREQUISITES:
Education:
  • Minimum B.S. degree in Analytical Chemistry, Biophysical/biochemical sciences, pharmaceutical sciences with 8 years industry experience
  • Or Master's Degree in Biochemistry, Biotechnology, Biology with 5+ years' experience in protein mass spectrometry
  • Or Ph.D. in Biochemistry, Biotechnology, Biology with 3+ years of experience in protein mass spectrometry

Experience:
  • A strong theoretical understanding and experience in protein chemistry and biochemistry.
  • In-depth hands-on experience with operation of HPLC, GC, dissolution, plate-readers and UV techniques is required.
  • An in-depth understanding of USP requirements, ICH guidelines and USP/EP pharmacopeia requirements
  • Excellent communication and technical writing skills
  • Experience in method development, as well as method qualification/verification/validation in a GLP/GMP environment
  • Strong experience in analytical method development and validation
  • Demonstrated skills as a team-player and team-management.
  • Ability to plan, schedule and work independently in a fast pace environment. Self-motivation, adaptability, and a positive attitude.
  • Working knowledge of applicable safety and standards guidelines, such as SOP, cGMP, GLP, DEA regulations and/or MSDS.
  • Ability to work under pressure and meet deadlines

SPECIALIZED KNOWLEDGE AND SKILLS:
  • Ability to multitask technical responsibilities in a fast-paced, dynamic environment is required
  • Proficiency with the following software is required: Microsoft Word, Excel, PowerPoint, and Outlook.
  • Experience with Mass Spectrophotometer is required.
  • Experience with Empower HPLC software programs is required.

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