Kedrion Biopharma

Chemistry Scientist

Kedrion Biopharma$70K — $116K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Chemistry or Biological Sciences.
  • Minimum of 5 years laboratory experience in the pharmaceutical industry.
  • Experience in chemical assays and analytical testing.
  • Familiarity with method development and laboratory instrumentation.
  • Strong knowledge of USP/EP compendia and regulatory requirements.
  • Proficient in Microsoft Office Suite.
  • Preferred: Experience with TrackWise and Lean Six Sigma tools.

Responsibilities

  • Perform advanced chemical and analytical testing on various samples.
  • Execute diverse laboratory techniques including HPLC, GC, and FTIR.
  • Draft and review technical documentation and analytical data.
  • Conduct statistical analysis for data trending and hypothesis testing.
  • Support method and equipment validation activities.
  • Train and mentor junior laboratory staff.
  • Collaborate across teams to drive quality and compliance.

Benefits

  • Medical, vision, and dental insurance
  • Life and AD&D insurance
  • Paid holidays
  • PTO accrual
  • And much more!
Full Job Description
Posting Start Date: 6/19/26

Country/Region: United States

State/Province: New York

Job Location: Melville

Place of Employment:

Contract Duration: Permanent

Hiring Pay Range Min: 70000

Hiring Pay Range Max: 95000

Chemistry Scientist

Job Summary

Drive scientific excellence and innovation in quality control-join our team as a Chemistry Scientist! In this role, you will perform advanced chemical testing across a full product line, including raw materials, in-process samples, and finished products. You will execute complex analytical procedures, generate and review technical documentation, and contribute to laboratory projects and validation activities. This position also plays a key role in mentoring junior staff, supporting compliance with regulatory standards, and collaborating across teams to ensure high-quality outcomes and continuous improvement within a dynamic QC Chemistry environment.

What you'll do

  • Perform advanced chemical and analytical testing on raw materials, in-process samples, and finished products.
  • Execute a variety of laboratory techniques, including pH, conductivity, HPLC, GC, FTIR, titration, and other analytical methods.
  • Draft and review laboratory documentation such as analytical data, technical reports, SOPs, investigations, and change controls.
  • Review data packages for release, stability, and in-process testing to support material disposition.
  • Conduct statistical analysis of data, including trending and hypothesis testing.
  • Support validation activities including method, equipment, and software IOQ/PQ initiativesc.
  • Develop and review protocols and reports for validation studies, assay development, and method transfers.
  • Operate, maintain, and troubleshoot laboratory instruments and resolve analytical issues.
  • Support internal and external audits to ensure compliance with regulatory and company requirements.
  • Ensure adherence to safety procedures, including proper handling and disposal of hazardous materials.
  • Assist with laboratory operations such as inventory management, equipment calibration, and housekeeping.
  • Collaborate cross-functionally and communicate effectively with team members and stakeholders.
  • Train and mentor junior staff while modeling company values and professional standards.
  • Contribute to continuous improvement initiatives and support CAPAs, deviations, and change control processes.


Qualifications and need-to-know

  • Bachelor's Degree in Chemistry or Biological Sciences.
  • Minimum of 5 years of related laboratory experience in the pharmaceutical industry, or equivalent combination of education and experience.
  • Experience performing chemical assays and analytical testing.
  • Experience with method development, validation, and laboratory instrumentation.
  • Strong knowledge of USP/EP compendia.
  • Working knowledge of cGMP, FDA, and regulatory requirements.
  • Proficiency in Microsoft Office Suite.
  • Strong written, verbal communication, and organizational skills.
  • Preferred: Experience with TrackWise, computer system validation (ISPE GAMP), and Lean Six Sigma tools.

Pay Range: $77,000.00-$116,000.00

Please note that salary ranges are calculated based off levels of: relevant experience, education, and certifications.

Kedrion Biopharma Inc. offers numerous benefits to our qualifying employees, including:
  • Medical, vision and dental insurance
  • Life and AD&D insurance
  • Paid holidays
  • PTO accrual
  • and much more!


Please let us know if you would like further details regarding the benefits that we offer to our qualifying employees, and we would be glad to provide you with our full benefits guide, as well as answering any questions you may have!

About Kedrion Biopharma

Kedrion Biopharma is a biopharmaceutical company that specializes in the development, production, and distribution of plasma-derived products for the treatment of rare and serious diseases. The company's product portfolio includes immunoglobulins, coagulation factors, and albumin, which are used to treat a variety of conditions, including immune deficiencies, bleeding disorders, and shock. Kedrion Biopharma operates in more than 100 countries worldwide and has a strong presence in Europe, North America, and Asia. The company is committed to improving the lives of patients with rare and serious diseases by providing high-quality, safe, and effective therapies. Kedrion Biopharma is headquartered in Fort Lee, New Jersey.
Learn more about Kedrion Biopharma
Size
2,500 employees
Industry

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