Quality Control Sr. Associate
Planet Pharma · Holly Springs, NC · 3 days ago
AnalystContract
Key Responsibilities
- Maintain required chain of custody of incoming samples in the Laboratory Information Management System (LIMS).
- Ensure proper labeling, storage, and chain-of-custody documentation for all samples.
- Evaluate and Document Results: Accurately record data, assess results for compliance with specifications, and ensure documentation meets GDP and GMP requirements.
- Troubleshoot and Resolve Issues: Identify technical and compliance issues within QC, and escalate or resolve them using defined procedures; collaborate with senior staff for complex problems.
- Support Investigations and Audits: Participate in laboratory investigations related to out-of-specification results or deviations; provide supporting documentation during audits.
- Cross-Functional Collaboration: Work closely with analysts and team leads across QC areas to meet project milestones and testing timelines.
- Continuous Improvement: Suggest process improvements and contribute to efficiency initiatives within QC labs.
Qualifications
- Bachelor’s degree preferred.
- 3–5 years of experience in a laboratory or sample management role.
- Familiarity with LIMS or other sample tracking systems preferred.
- Strong attention to detail and organizational skills.
- Ability to work in a fast-paced, regulated environment.
- Good communication and teamwork skills.
Schedule
Available to work on a 4/10 schedule (7:30am - 6pm), Sunday through Wednesday.