Quality Control Analyst II
About The Position
A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche. In Pharma Technical Development, we actively collaborate and develop creative technical solutions to efficiently transform scientific ideas into products that reliably deliver our pipeline to patients. As a Lab Analyst, you will join our Global Analytical Development and Quality Control team, a leader in developing and executing testing methods for our biologics pipeline. You will contribute to our mission through innovation, teamwork, and continuous improvement in a dynamic environment.
Requirements
- Bachelor's degree, preferably in a scientific discipline, or an Associate's degree with 5 years of related experience in a lab environment.
- Communicate clearly and effectively, both verbally and in writing.
- Exercise sound judgment, reasoning, and problem-solving capabilities.
- Demonstrate attention to detail with strong organization and prioritization skills.
- Take accountability and work effectively as part of a collaborative team.
Nice To Haves
- Previous GMP experience in a biopharmaceutics environment.
- QC / cGMP experience working in a lab environment in an industry or academic setting.
Responsibilities
- Perform a broad variety of basic and moderately complex physico-chemical tests for biologics and other pharmaceutical compounds according to GMP.
- Maintain accountability for deliverables affecting department goals and maintain a state of inspection readiness.
- Identify discrepancies and support the resolution of technical problems to assist the department in meeting corporate objectives.
- Schedule and execute routine and semi-routine assignments while supporting general lab maintenance operations.
- Ensure the integration of environmental health, safety, and security into business processes, reporting any safety and environmental incidents within your functional area.
- Adhere to cGMP policies and procedures, ensuring accurate documentation of activities and transactions in applicable systems.
- Coordinate with customers to support operational activities and actively participate in group and project teamwork.
Benefits
- A discretionary annual bonus may be available based on individual and Company performance.
- Benefits detailed at the link provided below.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
