Quality Control and Continuous Improvement Specialist I

Scorpion Therapeutics; Livermore (CA); On-site; USD 50,000 - 61,000; Full time

Job summary

Scorpion Therapeutics seeks a Quality Control & Continuous Improvement Specialist to drive on-site QC testing, data analysis, and process optimization at our operations. You will execute QC tests on raw, in-process, and finished materials and support continuous improvement to boost efficiency and compliance.

Role emphasizes lab testing, process validation, and GxP support in a regulated biopharma setting, with full on-site work. Salary starts at $55,000, depending on education and experience.

Qualifications

• Bachelor's in Life Sciences, Engineering, or related field.
• Knowledge of CAPA, regulatory standards, and process improvement methodologies.
• Strong analytical and communication skills.
• Prior experience with Lean, Six Sigma, FMEA, and statistical data analysis preferred.

Responsibilities

• Problem-solving using Lean, Six Sigma, and other tools, conducting root cause investigations, developing corrective actions.
• Collaborating with cross-functional teams to troubleshoot and refine processes.
• Maintaining documentation for regulatory compliance (e.g., AAALAC, USDA), supporting audits, and mentoring junior staff.

Skills

Lean

Six Sigma

CAPA

Regulatory standards

Data analysis

Communication

Education

Bachelor's in Life Sciences, Engineering, or related field

Job description

Role

Quality Control & Continuous Improvement Specialist responsible for on-site quality assurance, scientific testing, and process optimization at Inotiv's operational sites. Primary objectives include executing QC testing of raw, in-process, and finished materials, analyzing data for trends, and supporting continuous improvement initiatives to enhance operational efficiency and compliance.

Responsibilities

Responsibilities involve problem-solving using Lean, Six Sigma, and other tools, conducting root cause investigations, developing corrective actions, and collaborating with cross-functional teams to troubleshoot and refine processes. The role also entails maintaining documentation for regulatory compliance (e.g., AAALAC, USDA), supporting audits, and mentoring junior staff.

Requirements

• Bachelor's in Life Sciences, Engineering, or related field
• Knowledge of CAPA, regulatory standards, and process improvement methodologies
• Strong analytical and communication skills
• Prior experience with Lean, Six Sigma, FMEA, and statistical data analysis preferred

High-value: role demands full on-site presence, with a focus on quality control within a biopharma setting—likely involving work in regulated environments and supporting GxP compliance. Experience in laboratory testing, process validation, and operational excellence programs essential.

The position offers a salary starting at $55,000, with potential variation based on education and experience.