Overview In this role you support the Bioanalytical Sciences Quality Control team on site, performing QC review and contributing to documentation quality within established GxP processes. You will learn to interpret findings, collaborate with cross-functional stakeholders, and progressively handle QC tasks with supervision. This is a hands-on, growth-focused position in a fast-growing science-driven company where your work helps ensure documentation quality and compliance. You will be part of a mission-driven organization that translates science into medicines that help patients.
Compensation / Benefits- competitive total rewards package
- bonuses or incentive plans
- equity awards
- retirement benefits (e.g., 401(k) company match
- health and wellness programs
- paid time off
Responsibilities- Quality control review of documentation and acknowledging records
- Assemble resources to perform QC and evaluate documentation quality
- Manage multiple documentation types and multi-task effectively
- Develop foundational problem-solving approaches to resolve findings
- Collaborate with stakeholders across functions to improve documentation quality
- Participate in QC sub-team and group meetings and share results
- Provide cross-functional support to broaden exposure across the organization
Key requirements- Bachelor's or Master's degree and 0-3 years of relevant post-degree experience
- Foundational knowledge of GxP principles (preferred)
- Professional conduct, integrity, and strong work ethic
- Clear and concise communication and active listening
- Adaptability in a fast-paced environment
- Commitment to professional development and openness to feedback
- Curiosity and willingness to ask questions to deepen understanding
- clear communication
- collaboration
- adaptability
- professionalism
- GxP principles (foundational)
- documentation review and management
