Associate Scientist

Kelly Science, Engineering, Technology & Telecom; Cleveland (OH); On-site; USD 52,000 - 67,000; Full time

Job summary

An established industry player is seeking a passionate Associate Scientist to join their API Stability Laboratory team. This role offers the chance to engage with cutting-edge instrumentation while supporting the stability testing of small molecule drug substances in a fast-paced, cGMP-regulated environment. If you are detail-oriented and thrive on collaboration, this is an exciting opportunity to contribute to global healthcare initiatives. Join a team that values mentorship and innovation, and take your lab experience to the next level in a culture that encourages continuous learning and technical excellence.

Qualifications

• 2+ years of experience in a cGMP laboratory focused on analytical science.
• Familiarity with ICH stability guidelines and regulatory expectations.

Responsibilities

• Perform batch release and stability testing for APIs and drug products.
• Collaborate with clients to design and execute stability study plans.

Skills

HPLC

Assay Testing

Documentation Skills

Critical Thinking

Education

Bachelor’s degree in Chemistry

Job description

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Kelly Science has an immediate opening for an Associate Scientist for our growing client near Cleveland, OH

Full-time

Direct Hire

Are you passionate about analytical science and ready to take your lab experience to the next level?

We’re looking for a curious, motivated Associate Scientist to join our API Stability Laboratory team. In this role, you’ll work hands-on with cutting-edge instrumentation to support the stability testing of small molecule drug substances and drug products — all within a fast-paced, cGMP-regulated environment. If you have a keen eye for detail, thrive on scientific collaboration, and are ready to grow in a critical role supporting global healthcare, this is your opportunity.

What You’ll Do

• Perform batch release and stability testing for APIs and drug products under ICH and regulatory guidelines.
• Collaborate cross-functionally and with clients to design and execute effective stability study plans.
• Author and review protocols, reports, and data summaries with accuracy and clarity.
• Investigate and document out-of-specification (OOS) results, identify root causes, and support corrective actions.
• Manage lab inventory, maintain environmental chambers, and support compliance across lab systems.

What You Bring

• Education: Bachelor’s degree in Chemistry or related scientific field.
• Experience: At least 2 years of hands-on experience in an analytical or stability-focused cGMP laboratory.
• Familiarity with ICH stability guidelines and regulatory expectations (FDA, EMA).
• Practical knowledge of techniques like HPLC, assay/impurities testing, and solution prep.
• Strong documentation, communication, and critical thinking skills.
• A collaborative mindset and a passion for continuous learning in a regulated lab environment.

Why Join Us?

• Be part of a team that values mentorship, scientific rigor, and client-focused innovation.
• Gain exposure to diverse stability programs and cutting-edge methodologies.
• Work in a culture that encourages curiosity, growth, and technical excellence.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Science

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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