Associate III, Quality Control Raw Materials
Listed on 2026-01-01
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Quality Assurance - QA/QC
Quality Control / Manager, Quality Technician/ Inspector
This position is a M-F business hours schedule (8A-5P) and is full time on-site at our RTP facility
About This RoleAs an Associate III, QC Raw Materials, you will play an integral role in the Quality Control Raw Materials team at the Biogen RTP Pharma site. This critical position supports functional, tactical, and operational objectives by sampling, inspecting, and testing raw materials while maintaining strict adherence to cGMP documentation standards. Your expertise in Gas Chromatography (GC) and wet chemistry will be essential as you perform compendial testing and manage data entry into electronic laboratory information management and inventory systems.
Collaborating closely with QC teams, Quality, Planning, Warehouse, Validation, and Manufacturing teams, you will help ensure that operations run smoothly. Your role may also involve assisting with GMP compliance activities, investigation writing, and continuous improvement initiatives. By working independently and as part of a team, you will contribute significantly to the success of our quality assurance goals.
- Perform raw material sampling, inspections, and release testing.
- Conduct utility monitor samples to ensure quality standards.
- Provide technical review of data and documentation for QC Raw Materials.
- Support investigations and QC operations in alignment with business and manufacturing schedules.
- Assist in process validation initiatives to maintain compliance.
- Maintain effective laboratory systems to ensure the integrity of results.
- 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.
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 laboratory techniques make you a valuable asset to the team. You are dedicated to continuous improvement and ensure compliance with established processes and timelines.
RequiredSkills
- Bachelor's degree in science or related field.
- Minimum 2 years of relevant experience working in QC within a GMP pharma or biotech environment.
- Experience with Gas Chromatography (GC) and wet chemistry per compendia.
- Ability to move 50 lbs with the assistance of equipment as needed.
- Demonstrated technical ability in fundamental laboratory techniques and analytical methodology.
- Bachelor's degree in science or related field.
- Strong organizational skills with the ability to multitask and coordinate multiple activities.
- Excellent communication skills, both written and verbal.
- Ability to interpret data and draw conclusions.
Job Level: Professional
Additional InformationThe base compensation range for this role is: $68,000.00-$88,000.00
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; including, but not limited to:
- 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…
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