Quality Control: Raw Materials & Sample Management II

Scorpion Therapeutics; North Carolina; On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Healthcare benefits

Disability insurance

Vacation & holidays

Sick time

Parental leave & 401(k)

Employee stock plan

Tuition reimbursement

ERGs

Job summary

Scorpion Therapeutics seeks an Associate II, Quality Control to perform raw material sampling, inspections, and manage stability samples across testing labs. You will support QC operations and ensure alignment with manufacturing schedules.

You will enter data into ELIMS and inventory systems, help sustain 100% compliance, and collaborate with teams to support lab compliance and training. Requires a BS in science and 0–2 years GMP pharma/biotech experience; ability to lift 50 lbs.

Qualifications

• Bachelor’s degree in science or related field.
• 0–2 years of QC GMP pharma/biotech experience.
• Ability to move 50 lbs with assistance.
• Strong organizational skills and multitasking ability.
• Excellent written and verbal communication skills.

Responsibilities

• Perform raw material sampling and inspections
• Pick up and deliver samples to testing laboratories
• Manage stability samples and deliver to labs
• Support QC operations aligned with schedules
• Collaborate with teams to support laboratory compliance and personal development
• Enter data into electronic laboratory information management and inventory systems
• Manage retention samples and training to sustain 100% compliance

Skills

Organizational skills

Multitasking

Communication skills

Education

Bachelor’s degree in science or related field

Job description

Scorpion Therapeutics seeks an Associate II, Quality Control to perform raw material sampling, inspections, and manage stability samples across testing labs. You will support QC operations and ensure alignment with manufacturing schedules.

You will enter data into ELIMS and inventory systems, help sustain 100% compliance, and collaborate with teams to support lab compliance and training. Requires a BS in science and 0–2 years GMP pharma/biotech experience; ability to lift 50 lbs.