Associate II, Quality Control Raw Material and Sample Management

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

About This Role

As an Associate II, Quality Control, you will serve as a key member of the Quality Control Raw Materials/Sample Control team at the Biogen RTP Pharma site. In this role, you will be responsible for sampling and inspecting raw materials, as well as managing manufacturing, retain, and stability samples. You will ensure the proper handling, documentation, storage, distribution, and disposal of materials and samples in compliance with GMP requirements. Additionally, you will support laboratory operations through LIMS management, sample logistics, investigations, and other operational support activities. Working both independently and collaboratively, you will play an important role in achieving site quality objectives and maintaining compliance standards.

What You’ll Do

• Perform raw material sampling and inspections
• Pick up and deliver samples to the appropriate testing laboratories
• Manage stability samples and deliver them to labs at appropriate intervals
• Support QC operations in alignment with business and manufacturing schedules
• Collaborate with various 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

Who You Are

You are a detail-oriented professional passionate about maintaining high standards of quality. You excel in both independent and team environments, leveraging your strong written and verbal communication skills to contribute effectively. Your problem-solving abilities and technical expertise in sample handling make you a valuable asset to the team. You are dedicated to continuous improvement and ensure compliance with established processes and timelines.

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 the assistance of equipment as needed
• Strong organizational skills with the ability to multitask and coordinate multiple activities
• Excellent communication skills, both written and verbal

Job Level

Entry Level

Additional Information

The base compensation range for this role is: $57,000.00-$74,000.00. Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity. Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being;

• Medical, Dental, Vision, & Life insurances
• Fitness & Wellness programs including a fitness reimbursement
• Short- and Long-Term Disability insurance
• A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
• Up to 12 company paid holidays + 3 paid days off for Personal Significance
• 80 hours of sick time per calendar year
• Paid Maternity and Parental Leave benefit
• 401(k) program participation with company matched contributions
• Employee stock purchase plan
• Tuition reimbursement of up to $10,000 per calendar year
• Employee Resource Groups participation

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law.

Biogen is an E-Verify Employer in the United States.