Senior QC Laboratory Supervisor

Alora Pharmaceuticals

Fort Worth (TX)

On-site

USD 110,000 - 140,000

Full time

3 days ago
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Job summary

Alora Pharmaceuticals in Fort Worth, TX is seeking a QC Lab Supervisor to oversee qualitative and quantitative testing in support of drug products. You will supervise QC chemists, manage OOS/OOT investigations, and ensure training and adherence to cGMP and DEA regulations.

Requirements include a BA/BS in Chemistry or related field with 8+ years in a pharmaceutical QC lab, supervisory experience, and strong analytical and communication skills.

Qualifications

  • BA/BS in Chemistry or related scientific field with at least 8 years in a pharmaceutical QC lab.
  • Supervisory experience or coursework in supervision.
  • Strong organizational and detail oriented.
  • Highly accurate and efficient with abstract problem-solving skills.
  • Strong communication skills.

Responsibilities

  • Oversee QC lab testing of components, raw materials, in-process samples, finished products, and stability samples.
  • Schedule work to meet the needs of manufacturing, packaging, and the Customer.
  • Manage the timely completion of all OOS/OOT investigations.
  • Oversee the QC Laboratory Training Program and ensure timely training.
  • Support of Cleaning Validation and QA programs.
  • Supervise testing workflows and drive process improvements in the QC lab.
  • Ensure compliance with cGMP, DEA regulations, and quality procedures.
  • Coordinate development and implementation of quality assurance programs.

Skills

Strong communication skills
Analytical Chemistry understanding
Problem-solving skills
Leadership

Education

BA/BS in Chemistry or related scientific field
MS in Chemistry or related scientific field
Supervisory experience or supervision coursework

Tools

Excel (Advanced)

Job description

Alora Pharmaceuticals in Fort Worth, TX is seeking a QC Lab Supervisor to oversee qualitative and quantitative testing in support of drug products. You will supervise QC chemists, manage OOS/OOT investigations, and ensure training and adherence to cGMP and DEA regulations.

Requirements include a BA/BS in Chemistry or related field with 8+ years in a pharmaceutical QC lab, supervisory experience, and strong analytical and communication skills.

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