Senior QC Lab Supervisor – Pharmaceutical Testing

Sovereign Pharmaceuticals

Fort Worth (TX)

On-site

USD 90,000 - 140,000

Full time

33 hours ago
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Job summary

Sovereign Pharmaceuticals in Fort Worth, TX seeks a QC Lab Supervisor to oversee QC chemists in qualitative and quantitative analyses supporting raw materials, in-process samples, and finished products. You will manage OOS/OOT investigations, training programs, and lab workflows to ensure data integrity and regulatory compliance.

Ideal candidates have 8+ years in a pharmaceutical QC lab, with supervisory experience, strong communication, and problem-solving skills.

Qualifications

  • BA/BS in Chemistry or related field with strong laboratory experience in QC.
  • Minimum 8 years in a pharmaceutical QC lab with supervisory exposure.
  • Experience in cGMP environments and regulatory expectations.
  • Proven ability to manage and train staff in analytical workflows.
  • Strong documentation, data integrity, and problem-solving skills.
  • Effective communication with cross-functional teams and management.

Responsibilities

  • Supervise QC chemists performing qualitative and quantitative analyses.
  • Schedule work to meet manufacturing, packaging, and customer needs.
  • Oversee OOS/OOT investigations and timely completion.
  • Manage QC lab training programs and ensure timely completions.
  • Support cleaning validation and lifecycle quality programs.
  • Direct supervision of chemists and technicians in daily tasks.
  • Develop and implement QA programs aligned with production standards.

Skills

Supervisory experience
Strong communication skills
Abstract problem solving
Organized and detail oriented
Highly accurate and efficient

Education

BA/BS in Chemistry or related Scientific field
MS in Chemistry or related Scientific field

Tools

Advanced Excel

Job description

Sovereign Pharmaceuticals in Fort Worth, TX seeks a QC Lab Supervisor to oversee QC chemists in qualitative and quantitative analyses supporting raw materials, in-process samples, and finished products. You will manage OOS/OOT investigations, training programs, and lab workflows to ensure data integrity and regulatory compliance.

Ideal candidates have 8+ years in a pharmaceutical QC lab, with supervisory experience, strong communication, and problem-solving skills.

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