QC Chemist II

Scientific Search

Royston (GA)

On-site

USD 65,000 - 90,000

Full time

28 hours ago
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Benefits offered by this job

Competitive salary
Comprehensive benefits
Professional growth opportunities

Job summary

Scientific Search is assisting a leading pharmaceutical innovator in Royston, GA to recruit a QC Chemist. In this role you will conduct analyses of raw materials, intermediates, and finished products to ensure compliance with quality specifications.

You will validate analytical methods per ICH/FDA/USP, review data, transfer methods with stakeholders, calibrate instruments, and support continuous improvement in a fast-paced manufacturing environment.

Qualifications

  • Minimum 2 years' industrial experience in Quality Control laboratory functions, specifically with HPLC.
  • Bachelor's degree in Biology, Chemistry, Biochemistry, or a related field.

Responsibilities

  • Performing detailed analysis of raw materials, finished products, and stability samples.
  • Validating analytical methods according to ICH, FDA, USP, BP, EP etc., for a wide range of formulations.
  • Reviewing analytical data and performing method transfer activities with various stakeholders.
  • Ensuring products meet all specifications through rigorous analytical testing.
  • Calibration and maintenance of analytical instruments.

Skills

HPLC
Quality Control
Method Validation
Data analysis

Education

Bachelor's degree in Chemistry/Biology/Biochemistry

Tools

HPLC instruments

Job description

QC Chemist

Royston, GA

Are you ready to propel your career in the pharmaceutical industry and make a meaningful impact in healthcare? If you're passionate about chemistry and eager to contribute to the forefront of pharmaceutical manufacturing, this opportunity is your gateway to a thriving career. Join our client, a leader in pharmaceutical innovation, as a QC Chemist and play a pivotal role in ensuring the highest quality of life-saving products.

Why You Should Apply
  • Be part of an organization that is at the cutting edge of pharmaceutical manufacturing.
  • Engage in critical analysis of raw materials and finished products using advanced HPLC/UV techniques.
  • Opportunity to master Analytical Method Validation in line with global regulatory standards.
  • Benefit from a collaborative environment that fosters professional growth and learning.
  • Competitive salary package and comprehensive benefits.
What You'll Be Doing
  • Performing detailed analysis of raw materials, finished products, and stability samples.
  • Validating analytical methods according to ICH, FDA, USP, BP, EP etc., for a wide range of formulations.
  • Reviewing analytical data and performing method transfer activities with various stakeholders.
  • Ensuring products meet all specifications through rigorous analytical testing.
  • Calibration and maintenance of analytical instruments.
About You
  • Minimum 2 years' industrial experience in Quality Control laboratory functions, specifically with HPLC.
  • A Bachelor's degree in Biology, Chemistry, Biochemistry, or a related field.
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