Sr Scientist

Posted 4 Days Ago
Be an Early Applicant
Melrose Park, IL, USA
In-Office
95K-110K Annually
Senior level
Healthtech • Pharmaceutical
The Role
Serve as subject-matter expert for extractables and leachables (E&L) and mass spectrometry. Design, perform, and evaluate E&L studies in a cGMP lab, including method development, validation, troubleshooting instruments (GC/MS, HR-LC/MS, LC/MS, ICP/MS), spectral interpretation, drafting protocols/reports, preparing regulatory dossier summaries, training junior scientists, and leading projects to meet regulatory standards (USP/ISO/21 CFR).
Summary Generated by Built In
Job SummaryResponsible for technical evaluation of extractable and leachable studies to ensure that acceptable data is generated to
support FDA drug applications. This role will be responsible for providing technical training to other scientists and will
serve as a subject matter expert for mass spectrometry and extractable and leachable.
This position is located in our Innovation and Development Center in Melrose Park, IL.
Salary Range: $95,000-110,000
Position is eligible to participate in a bonus plan with a target of 6% of the base salary
Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.
Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most. Benefits offered include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage.

Responsibilities

1. Reviews extractable/leachable study design concepts to meet regional requirements (i.e., USP <1663> and <1664> or ISO 10993).

2. Performs Extractable and Leachable testing in the lab, which includes method development, Method validation, and stability testing in a cGMP environment.

3. Acts as a subject matter expert in mass spectrometry and extractable/leachable

4. Operates and troubleshoots the GC/MS, HR-LC/MS, and other analytical methods used for extractable and leachable Testing in a cGMP environment.

5. Evaluate analytical results and identify trends/exceptions/interpretations of results relative to chemical characterization, product requirements, and toxicological assessment.

6. Draft, review, and approve E&L analytical testing protocols and reports.

7. Performs mass spectral interpretation and unknown compound identification. 8. Prepares E&L studies and safety assessment summaries for regulatory dossiers.

9. Understand and effectively communicate the strategic focus and plan to team members.

10. Communicates clearly with the manager, peers, cross-functional teammates, and non-technical audiences by openly sharing project status and hurdles while seeking input from other team members.

11. Other duties as assigned.

Requirements

  • Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biological Sciences with 5+ years of related experience or a master’s degree in Pharmaceutical Sciences, Chemistry, Biological Sciences with 3+years of related experience or a PhD in Pharmaceutical Sciences, Chemistry, Biological Sciences, Chemical/Biomedical 
  • Engineering with one to three years of related experience is required.  
  • In-depth knowledge of Analytical Chemistry or Pharmaceutical Science and various Mass spectrometers is required.
  • The ability to apply chemistry knowledge for problem-solving and innovative approaches in Method development, Method Validation, and analytical testing is required. 
  • Prior knowledge and work experience in extractable, leachable, and impurity identification is a plus. 
  • Knowledge and Hands-on experience in various mass spectrometric operations, troubleshooting, and reporting tools are required.
  • A candidate with experience in any one of Agilent’s HS-GC/MS, GC-MS, LC/MS, and ICP/MS instruments to aid in data interpretation of chemical characterization of E&L compounds and for method qualification/validation under a cGMP environment is highly preferable. 
  • Knowledge and experience in mass spectral interpretation and unknown compound identification.  
  • Clear understanding of FDA and other regulatory expectations concerning extractable and leachable (e.g., relevant ISO, USP, EP, JP, 21 CFR sections, and industry standards is preferable 
  • Candidate should be able to manage multiple projects and new scientific initiatives simultaneously, independently, with others, and as part of a team. Expected to execute all E&L projects with detail and discipline and achieve all project milestones on time. 
  • Expected to lead E/L project activities with minimum guidance and supervision.  
  • Able to train junior scientists and strongly desire to learn and contribute to the company's business needs. 
  • Provided constructive feedback to E&L and analytical colleagues and motivated other team members as required.
  • Candidate should be able to write, review, and approve analytical methods, validation protocols and reports, E&L testing reports, SOPs, technical memos, Investigation reports, change control, and E&L part of the regulatory dossiers. 
  • Excellent written and verbal communication skills 
  • Flexible, adaptive, strong desire to work in a dynamic environment, responsive to urgency. 
  • Self-motivated, empowered personality, result- and deadline-oriented 
  • Strong organizational skills, attention to detail, interpersonal skills, and ability to manage competing priorities are essential for success. 
  • Must be willing to perform drug product testing for potent compounds, cytotoxic substances, and/or controlled substances while following and observing all safety procedures in place, which include the use of engineering controls, administrative controls, Standard Operating Procedures 
  • The Company’s primary business language is English. The successful candidate must be able to effectively speak, read, write, and understand English to perform the essential functions of the position, including independently understanding policies, procedures, training materials, and workplace communications written in English due to our heavily regulated work environment.

Additional Information

We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability, 401K with company contribution, and wellness program.

Please note that joining our team does not create a guaranteed or permanent employment arrangement. All employment is at‑will, meaning both the employee and Fresenius Kabi have the right to end the employment relationship at any time, in accordance with applicable federal and state laws.

Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.

Skills Required

  • Bachelor's degree in Pharmaceutical Sciences, Chemistry, or Biological Sciences with 5+ years related experience OR Master's with 3+ years OR PhD with 1-3 years
  • In-depth knowledge of Analytical Chemistry and various mass spectrometers
  • Experience in method development, method validation, and stability testing in a cGMP environment
  • Hands-on experience operating and troubleshooting GC/MS, HR-LC/MS, LC/MS, or ICP/MS and related analytical methods
  • Mass spectral interpretation and unknown compound identification
  • Prior knowledge and work experience in extractable, leachable, and impurity identification
  • Experience with Agilent HS-GC/MS, GC-MS, LC/MS, or ICP/MS instruments (for data interpretation and method qualification/validation)
  • Understanding of FDA and other regulatory expectations concerning E&L (relevant ISO, USP, EP, JP, 21 CFR)
  • Ability to draft, review, and approve analytical methods, validation protocols, E&L testing reports, SOPs, technical memos, investigation reports, change control, and regulatory dossier sections
  • Ability to evaluate analytical results, identify trends/exceptions, and prepare safety assessment summaries for regulatory dossiers
  • Ability to lead E&L project activities, manage multiple projects, and train junior scientists with minimum guidance
  • Excellent written and verbal communication skills and ability to work in English
  • Willingness to perform drug product testing for potent, cytotoxic, and/or controlled substances following safety procedures
  • Strong organizational skills, attention to detail, and ability to meet deadlines in a dynamic environment
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The Company
HQ: Bad Homburg v. d. Höhe
21,388 Employees

What We Do

Fresenius Kabi is a global healthcare company that specializes in lifesaving medicines and technologies for infusion, transfusion, and clinical nutrition. The company’s products and services are used for the therapy and care of critically and chronically ill patients. Its product portfolio comprises a range of highly complex biopharmaceuticals, clinical nutrition, medical technologies, and I.V. generic drugs. Within biopharmaceuticals, Fresenius Kabi offers, among others, biosimilar drugs with a focus on autoimmune diseases and oncology. The company’s clinical nutrition offering includes a wide selection of enteral and parenteral nutrition products. In the segment of medical technologies, its offering includes vital disposables, infusions pumps, apheresis machines, cell therapy devices, and more. Fresenius Kabi puts essential medicines and technologies in the hands of people who help patients and finds the best answers to the challenges they face. Following its strategy “Vision 2026”, which is a key part of the #FutureFresenius program of the Fresenius healthcare group, the company is furthermore committed to increase efficiencies in the therapy and care of patients and improve access to high-quality healthcare around the globe. Fresenius Kabi aspires to be leading globally in its product segments – all for the benefit of patients, its customers, and its stakeholders. Fresenius Kabi Community Guidelines and User Information: https://www.fresenius-kabi.com/social-media-terms-conditions Imprint: https://www.fresenius-kabi.com/imprint

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