Quality Control Associate
Target PR Range: 22-32/hr
*Depending on experience
- Ensure proper labeling, storage, and chain-of-custody documentation for all samples.
- Perform Analytical Testing: Prepare and execute routine and complex testing procedures for bioassay, chemistry, and microbiology following established protocols and regulatory standards.
- 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 issues during testing and escalate or resolve them using defined procedures; collaborate with senior staff for complex problems.
- Maintain Laboratory Equipment: Operate, calibrate, and perform basic maintenance on laboratory instruments (e.g., HPLC, ELISA platforms, microbiological incubators) to ensure readiness for testing.
- 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.
- Compliance and Safety: Adhere to all safety guidelines, SOPs, and regulatory requirements while performing testing and handling hazardous materials. Qualifications: - Associate degree in a scientific discipline or equivalent experience; Bachelors degree preferred.
- 1-3 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.
- Available to work night shifts (10 PM - 8 AM) on a 4/10 schedule.
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