Associate II, Quality Control Raw Material and Sample Management
Biogen
August 25, 2026
On-site
Triangle, NC
Operations
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
- 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