SCIENTIST (Chemistry) - 3rd Shift (Overnights)

Fresenius Kabi USA

Town of Grand Island (NY)

On-site

USD 33,311 - 47,443

Full time

14 days+

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Benefits offered by this job

Medical coverage
Dental coverage
Vision coverage
401(k) with company contribution
Wellness program

Job summary

A leading pharmaceutical company in Grand Island is seeking a Scientist I in Quality Control to perform analytical chemistry and chromatographic methods while providing guidance. The ideal candidate must have a BS in a relevant field and 2+ years of pharmaceutical experience. Responsibilities include testing, troubleshooting, and ensuring compliance with documentation protocols. This role offers a competitive salary and an excellent benefits package including medical and retirement options.

Qualifications

  • Typical 2+ years of related experience in the pharmaceutical industry.
  • Familiarity with cGMP and FDA regulations is essential.
  • Proficient in Microsoft Office (Word, Excel) and flexible with changing projects.

Responsibilities

  • Articulate work-related issues clearly to management and peers.
  • Perform routine testing using instrumental methods of analysis.
  • Update and route SOPs, MOAs, Specifications.
  • Troubleshoot instrumentation and apply problem solving skills.
  • Document testing in compliance with good practices.

Skills

Analytical chemistry
Chromatographic methods
Troubleshooting
Microsoft Office
Good Documentation Practices

Education

BS in Chemistry, Biology, or related physical science

Tools

HPLC
TLC
FTIR
pH
UV-Vis
Empower

Job description

Shift: 1st Shift 6:00 AM to 2:30 PM, Monday through Friday.

Hourly Rate: $29.31/hour (final pay based on experience, education, knowledge, skills, and abilities).

Job Summary

A Scientist I in Quality Control responsible for analytical chemistry, chromatographic methods including troubleshooting. Directs and provides guidance to associate scientists.

Responsibilities
  • Be able to articulate work related issues clearly and effectively to management and peers.
  • Perform accurate routine testing utilizing instrumental methods of analysis (HPLC, TLC, FTIR, pH, UV-Vis) with emphasis on chromatography to meet departmental objectives.
  • Update and route SOPs, MOAs, Specifications through Documentum as delegated by supervisor.
  • Perform troubleshooting of instrumentation by applying problem solving skills.
  • Provide guidance to Associate Scientist personnel when necessary.
  • Document testing in compliance with Good Documentation Practices.
  • Manage work and time based on departmental priorities using own judgement and objective reasoning.
  • Perform peer review of data to ensure compliance and accuracy.
Requirements
  • BS in Chemistry, Biology, or related physical science; typical 2+ years of related experience in the pharmaceutical industry with familiarity with cGMP and FDA regulations.
  • Hands‑on experience and knowledge of chromatographic methods and related chromatography data systems (e.g., Empower). Proficient in Microsoft Office (Word, Excel). Must be flexible with continually changing projects and priorities.
Additional Information

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

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.

Seniority Level
  • Entry level
Employment Type
  • Full-time
Job Function
  • Research, Analyst, and Information Technology
Industries
  • Pharmaceutical Manufacturing
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