Associate II, Quality Control Raw Material and Sample Management

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

Associate II, Quality Control — Responsibilities:

• Perform raw material sampling and inspections
• Pick up and deliver samples to appropriate testing laboratories
• Manage stability samples and deliver them to labs at appropriate intervals
• Support QC operations aligned with business and manufacturing 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

Qualifications / Required Skills:

• Bachelor’s degree in science or related field
• 0–2 years of relevant experience working in QC within a GMP pharma or biotech environment
• Ability to move 50 lbs with assistance of equipment as needed
• Strong organizational skills; ability to multitask and coordinate multiple activities
• Excellent written and verbal communication skills

Benefits (as listed):

• Medical, dental, vision, and life insurances; fitness & wellness programs (fitness reimbursement)
• Short- and long-term disability insurance
• 15+ days paid vacation and end-of-year shutdown (Dec 26–Dec 31)
• Up to 12 paid holidays + 3 personal significance days; 80 hours sick time/year
• Paid maternity and parental leave; 401(k) with company match
• Employee stock purchase plan; tuition reimbursement up to $10,000/year
• Employee Resource Groups participation