Associate, Scientist, Method Development

Astrix; Cleveland (OH); On-site; USD 70,000 - 80,000; Full time

Job summary

A leading company in the biotechnology and pharmaceutical manufacturing sector is seeking an Associate Scientist to support analytical stability studies in a cGMP laboratory. The ideal candidate will have hands-on experience with small molecule drug substances and drug product batch release. Responsibilities include performing HPLC analysis, coordinating stability testing, and ensuring compliance with regulatory guidelines. This full-time position offers a competitive salary based on experience and skills.

Benefits

Medical insurance

Vision insurance

401(k)

Qualifications

• 2+ years related pharmaceutical analytical laboratory experience required.
• Experience in GLP/cGMP and laboratory quality control desired.

Responsibilities

• Perform routine HPLC analysis in a GMP analytical laboratory.
• Coordinate stability testing and write protocols and reports.
• Review data for technical content and good record keeping practices.

Skills

HPLC

NMR

Mass Spec

Communication

Multitasking

Education

B.S. in Chemistry

Tools

Microsoft Excel

Microsoft Word

Job description

Associate, Scientist, Method Development

Associate, Scientist, Method Development

This range is provided by Astrix. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$70,000.00/yr - $80,000.00/yr

Direct message the job poster from Astrix

Scientific and technical staffing leader connecting top talent with industry-leading companies

• Direct Hire
• Shift: 1st shift 8a-5p M-F
• Top 3 requirements:

1 - Needs to have experience with HPLC, NMR and Mass Spec

2 - Coming from a GMP Lab environment is needed

3 - 2 Years of working experience - relevant analytical Lab environment.

Position Summary

We are seeking a detail-oriented and proactive Associate Scientist to join our cGMP Laboratory. This role involves supporting analytical stability studies in compliance with regulatory guidelines. The ideal candidate will have hands-on experience with small molecule drug substances and drug product batch release and stability testing, and experience working in a cGMP environment.

• Perform routine HPLC analysis in a GMP analytical laboratory
• May also perform FTIR, GC, NMR, MS, KF, XRD, DSC, TGA, and other analyses
• Coordinate stability testing, write protocols and reports
• Coordinate the timely and compliant generation of data to support client projects
• Review data for technical content and good record keeping practices
• Other duties as assigned

Requirements Educational Qualifications

• Minimum B.S. in chemistry with 2+ years related pharmaceutical analytical laboratory experience or equivalent combination of education and experience is required. Relevant experience in good laboratory/manufacturing practices (GLP/cGMP), laboratory quality control or stability, and interaction with quality assurance is desired.

Specific Skills and Requirements

• Experience with HPLC equipment and analysis
• Experience with FTIR, GC, NMR, MS, KF, XRD, DSC, TGA, desired but not required
• Experience with standard lab equipment (balances, pipettes, pH meter, etc.)
• Proficient in Microsoft Excel and Word
• Must have basic chemical knowledge and be able to handle materials safely
• Must be able to communicate effectively with manufacturing and quality personnel.
• Must be able to effectively multitask.

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science, Research, and Quality Assurance

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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