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Biosimilars Jobs (NOW HIRING)

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Biosimilars information

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$150K

$188.7K

$232.5K

How much do biosimilars jobs pay per year?

As of Jun 10, 2026, the average yearly pay for biosimilars in the United States is $188,749.00, according to ZipRecruiter salary data. Most workers in this role earn between $167,500.00 and $210,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Biosimilars position, and why are they important?

To thrive in a Biosimilars role, you typically need a background in life sciences or pharmacy, in-depth understanding of biologic drug development, and knowledge of regulatory requirements such as those from the FDA or EMA. Familiarity with laboratory techniques, clinical trial management systems, and compliance software is highly valuable, along with certifications in clinical research or regulatory affairs. Excellent analytical skills, attention to detail, and the ability to work collaboratively across multidisciplinary teams set top candidates apart. These skills are crucial to ensure strict adherence to regulatory standards and to bring safe, effective biosimilar therapies to market efficiently.

What job makes $10,000 a month without a degree?

In the field of biosimilars, roles such as pharmaceutical sales representatives or medical science liaisons can earn around $10,000 per month, often requiring strong industry knowledge, sales skills, and relevant certifications rather than a traditional degree. These positions typically involve working in healthcare or pharmaceutical companies and may require experience or specialized training in the biotech or medical fields.

What are some common challenges faced by professionals working in biosimilars development and how are they addressed?

Professionals in biosimilars development often face challenges such as navigating complex regulatory pathways, demonstrating biosimilarity to reference biologics, and ensuring consistent product quality throughout manufacturing. Teams address these challenges by maintaining close communication with regulatory agencies, applying rigorous analytical methods, and implementing strong quality assurance processes. Collaboration across regulatory, clinical, and manufacturing departments is essential to successfully bring a biosimilar to market. Staying updated on evolving industry standards and regulatory expectations is also key to overcoming obstacles in this fast-paced field.

What is a Biosimilars job?

A Biosimilars job typically involves working in the development, manufacturing, regulation, or commercialization of biosimilar medicines—biological products that are highly similar to approved reference biologics. Professionals in this field may work in areas such as research and development, quality control, clinical trials, regulatory affairs, or marketing. Roles can include scientists, regulatory specialists, project managers, or sales professionals, depending on the company and stage of product development. The goal of a biosimilars job is to ensure these medicines meet rigorous safety, efficacy, and quality standards while providing more affordable treatment options for patients.

More about Biosimilars jobs
What are the most commonly searched types of Biosimilars jobs? The most popular types of Biosimilars jobs are:
What states have the most Biosimilars jobs? States with the most job openings for Biosimilars jobs include:
Infographic showing various Biosimilars job openings in the United States as of June 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $188,749 per year, or $90.7 per hour.
Principal Scientist Bioseparation & Analytical Development

Principal Scientist Bioseparation & Analytical Development

Element Materials Technology

Ann Arbor, MI

Full-time

Posted 2 days ago


Element Materials Technology rating

7.5

Company rating: 7.5 out of 10

Based on 41 frontline employees who took The Breakroom Quiz

55th of 103 rated laboratories


Job description

Element Ann Arbor is currently seeking a highly experienced Principal Scientist – Bioseparation to lead and execute advanced analytical method development, characterization, and validation of large molecule therapeutics across discovery, development, and late-stage CMC. This is an onsite, laboratory-based role with significant hands-on responsibility in bioseparation sciences, supporting a broad range of biologics modalities including proteins and recombinant proteins, peptides and peptide-drug conjugates, monoclonal antibodies (mAbs) and biosimilars, antibody-drug conjugates (ADCs), mRNA therapeutics, DNA constructs (including plasmid DNA and oligonucleotides), viral vectors, and other complex or emerging modalities such as fusion proteins, multispecifics, and engineered biologics.


  • Lead development, optimization, and troubleshooting of bioseparation-based analytical methods supporting biologics across discovery, development, and late-stage CMC, including orthogonal analytical strategies for comprehensive characterization
  • Perform hands-on execution and technical leadership across a broad range of modalities, including proteins and recombinant proteins, peptides and peptide-drug conjugates, monoclonal antibodies (mAbs) and biosimilars, antibody-drug conjugates (ADCs), mRNA therapeutics, DNA/plasmid DNA/oligonucleotides, viral vectors, and emerging complex biologics (fusion proteins, multispecifics, engineered constructs)
  • Apply deep expertise in chromatography platforms (HPLC/UPLC/UHPLC, SEC, IEX, HIC, RP-HPLC, affinity chromatography), mass spectrometry (LC-MS/MS, high-resolution MS, SEC-MALS, native MS, MAM workflows, glycan/PTM characterization), capillary electrophoresis (CE-SDS, cIEF, purity/identity assays), and supporting biophysical techniques (DLS, DSC, UV/fluorescence, MALS, CD, FTIR)
  • Lead analytical strategy for complex biologics programs, including method development, qualification, validation, transfer, comparability, stability, forced degradation, and full characterization studies
  • Ensure development of robust GMP-compliant methods aligned with ICH Q2/Q6, USP, EP, and GMP requirements, and support regulatory submissions (IND, BLA, IMPD) with high-quality analytical data packages
  • Drive innovation in analytical science, including implementation of MAM workflows, high-throughput LC-MS platforms, automated bioseparation methods, and evaluation of emerging technologies in biologics characterization
  • Provide scientific leadership and mentorship to junior scientists, including troubleshooting complex bioseparation and mass spectrometry challenges and establishing best practices in analytical development and execution

  • BS in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or related field required; Master's degree or higher preferred, but not required.
  • Extensive industry experience in biologics analytical development is highly desirable
  • 8–15+ years of experience in biopharmaceutical or CRO analytical development with strong hands-on expertise in bioseparation of large molecules
  • Deep technical expertise across analytical platforms, including LC/UPLC/SEC/IEX/HIC/RP chromatography, LC-MS and high-resolution mass spectrometry, CE-SDS, cIEF, SEC-MALS, and complementary biophysical techniques
    Strong scientific knowledge of protein structure and higher-order structure, monoclonal antibodies and biosimilars, antibody-drug conjugates (ADCs), engineered biologics, and nucleic acid-based therapeutics (mRNA, DNA, oligonucleotides)
  • Demonstrated experience in comparability, stability studies, and degradation pathway analysis for complex biologics
  • Preferred experience includes CRO or client-facing analytical project execution, MAM workflows, advanced LC-MS analytics, glycan mapping and PTM quantification, and automation/high-throughput analytical systems
  • Strong scientific writing capability with experience supporting regulatory documentation and submissions
  • Proven ability to execute in onsite laboratory environments with strong hands-on bioseparation and multi-platform analytical integration skills
  • Ability to manage complex biologics programs in fast-paced, matrixed environments with strong problem-solving and scientific reasoning capabilities
  • Effective communicator across scientific, regulatory, and operational stakeholders

Physical Demands:

  • Frequency of required physical force: Minimum (moderate)
  • Lifting requirements: lifting <50 lbs. often and >50 lbs. on occasion
  • Ability to stand on feet for long periods of time
  • Ability to lift 50+lbs periodically

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Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to ‘Make tomorrow safer than today’.

When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access.

While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development.

Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization.


At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming “the world’s most trusted testing partner”.

All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws.


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