Senior QC Lab Analyst — Method Dev & Validation

Actalent

Elwood (KS)

On-site

USD 43,000 - 56,000

Full time

2 hours ago
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Job summary

Actalent is seeking a QC Specialist/Biochemist in Elwood, KS to lead day-to-day QC laboratory activities and serve as the SME for key instruments. You will perform routine release testing, drive method development and validation, and support technical transfers to ensure robust, compliant analytical practices.

The role emphasizes leadership, safety, and continuous improvement with cross-functional collaboration in a fully onsite laboratory environment.

Qualifications

  • 4+ years in QC or related analytical environment.
  • Bachelor's degree in Biochemistry, Biological Sciences, Pharmaceutical Sciences, or related field; advanced degree preferred.
  • Hands-on experience with HPLC and ELISA techniques in an analytical lab.
  • Experience in leadership or training roles within a laboratory environment.

Responsibilities

  • Direct the daily workload of QC Technicians and Specialists, ensuring QC policies and standards are followed.
  • Serve as the primary point of contact for technical instruction and troubleshooting for the QC team.
  • Perform routine release testing to support product and material disposition per methods and specs.
  • Lead method development, optimization, and improvement activities; participate in validation.
  • Lead technical transfers of analytical methods with proper documentation.
  • Lead quality events and investigations with timely, thorough resolutions.
  • Review and approve QC documentation for accuracy and compliance.
  • Audit inventory management in the laboratory for proper control and labeling.

Skills

Quality control
Leadership
Communication
Data integrity

Education

Bachelor's in Biochemistry / related
Advanced degree (Masters/PhD) preferred

Tools

HPLC
ELISA
Empower software

Job description

Actalent is seeking a QC Specialist/Biochemist in Elwood, KS to lead day-to-day QC laboratory activities and serve as the SME for key instruments. You will perform routine release testing, drive method development and validation, and support technical transfers to ensure robust, compliant analytical practices.

The role emphasizes leadership, safety, and continuous improvement with cross-functional collaboration in a fully onsite laboratory environment.

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