QC Raw Materials & Sample Management Associate II

Biogen, Inc.; Northern (KY); Hybrid; USD 57,000 - 74,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

Wellness programs

Disability Insurance

Vacation & shutdown

Holidays & Personal Days

Sick Time

Parental Leave

401(k) Plan

Employee Stock Purchase Plan

Tuition Reimbursement

Employee Resource Groups

Job summary

Biogen is seeking an Associate II, Quality Control, at the RTP Pharma site. You will sample and inspect raw materials, manage samples, and support QC operations to ensure GMP compliance and timely lab testing.

You will handle data entry in LIMS and participate in retention activities to maintain 100% compliance. The role requires a Bachelor’s degree in science or related field with 0–2 years in QC within GMP pharma or biotech, and the ability to move 50 lbs with equipment.

Qualifications

• Bachelor's degree in science or related field.
• 0-2 years of relevant QC experience in GMP pharma or biotech.
• Ability to move 50 lbs with equipment.
• Strong organizational and multitasking abilities.
• Excellent written and verbal communication.

Responsibilities

• Perform raw material sampling and inspections.
• Pick up and deliver samples to testing laboratories.
• Manage stability samples and deliver to labs at intervals.
• Support QC operations in alignment with schedules.
• Collaborate with teams to support laboratory compliance.
• Enter data into electronic laboratory information management and inventory systems (LIMS).
• Manage retention samples and training to sustain 100% compliance.

Skills

Excellent communication skills

Strong organizational skills

Detail-oriented

Ability to move 50 lbs with equipment

Education

Bachelor's degree in science or related field

Job description

Biogen is seeking an Associate II, Quality Control, at the RTP Pharma site. You will sample and inspect raw materials, manage samples, and support QC operations to ensure GMP compliance and timely lab testing.

You will handle data entry in LIMS and participate in retention activities to maintain 100% compliance. The role requires a Bachelor’s degree in science or related field with 0–2 years in QC within GMP pharma or biotech, and the ability to move 50 lbs with equipment.