Associate Chemist

Astrix; Concord (OH); On-site; USD 65,000 - 75,000; Full time

Job summary

Join a forward-thinking company as an Associate Chemist, where you will support analytical stability studies in a cGMP environment. This role offers the chance to work with a global leader in pharmaceutical ingredients, ensuring compliance with regulatory guidelines while developing your expertise in stability testing and quality control. If you are detail-oriented and proactive, this opportunity allows you to make a significant impact in a dynamic team dedicated to excellence in the pharmaceutical industry.

Benefits

Medical insurance

Vision insurance

401(k)

Qualifications

• 2+ years of relevant analytical lab experience in a cGMP environment.
• Hands-on experience with small molecule drug substances.

Responsibilities

• Conduct stability testing in a cGMP-regulated lab.
• Coordinate timely generation of stability data for client projects.
• Perform OOS investigations and implement corrective actions.

Skills

Analytical Laboratory Skills

cGMP Compliance

Stability Testing

Root Cause Analysis

Education

Bachelor’s degree in Chemistry

Job description

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

$65,000.00/yr - $75,000.00/yr

Direct message the job poster from Astrix

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

Our client is a global leader that helps develop and produce active pharmaceutical ingredients for their CDMO Partners and Generics. Join the team as an Associate Chemist. This is a great opportunity to work with an industry leader that focuses on their expertise and competence in all the companies’ processes.

Shift: Monday-Friday 8a-5p

Type: Direct Hire

Pay: $65,000-$75,000

We are seeking a detail-oriented and proactive Associate Scientist to join our cGMP API Stability 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.

Requirements:

• Bachelor’s degree in Chemistry or a related scientific discipline required.
• Minimum of 2 + years of relevant analytical laboratory experience in a cGMP environment, or an equivalent combination of education and experience.
• Relevant experience in a quality control or stability laboratory is essential

Responsibilities:

• Conduct stability testing and support activities in a cGMP-regulated laboratory.
• Coordinate the timely and compliant generation of stability data to support client projects.
• Perform out of specification (OOS) investigations, identify potential root causes, and support implementation of corrective actions.
• Review laboratory data for technical accuracy and regulatory compliance.
• Manage laboratory inventory, environmental chambers, and related information systems.
• Collaborate with clients to design appropriate batch release and stability studies for APIs and drug products.
• Develop and maintain expertise with applicable ICH, FDA, and EMEA stability guidelines.

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 and Other

• Industries

  Chemical Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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