Associate Quality Control

Note: Fully Onsite
All candidates must be available to work on night shift schedule after training
1st 3 – 6 months will be dayshift (training) – 4/10 schedule
After the training it will be 4/10 night shift schedule

The associate will begin training in sample management the first 3 – 6 months, 4/10 day shift schedule with cross-training to support additional laboratory areas, including chemistry, bioassay, and microbiology. The long term expectation will require the associate to work a 4/10 night shift schedule (Sunday-Wednesday or Wednesday-Saturday) from 10:00 PM to 8:00 AM. The Associate, Quality Control supports sample management and laboratory testing activities within the Quality Control department.

This role is responsible for the receipt, handling, tracking, storage, and disposal of samples used in analytical testing, while ensuring compliance with internal SOPs, regulatory requirements, and good documentation practices. The associate will collaborate closely with laboratory analysts, Quality Assurance, and other cross‑functional teams to maintain efficient and accurate testing workflows.

• Ensure proper labeling, storage, and chain-of-custody documentation for all samples.
• Prepare and execute routine and complex testing procedures for bioassay, chemistry, and microbiology following established protocols and regulatory standards.
• Accurately record data, assess results for compliance with specifications, and ensure documentation meets GDP and GMP requirements.
• Identify technical issues during testing and resolve or escalated using defined procedures.
• Operate, calibrate, and perform basic maintenance on laboratory instruments (e.g., HPLC, ELISA platforms, microbiological incubators) to ensure readiness for testing.
• Participate in laboratory investigations related to out-of-specification results or deviations; provide supporting documentation during audits.
• Work closely with analysts and team leads across QC areas to meet project milestones and testing timelines.
• Suggest process improvements and contribute to efficiency initiatives within QC labs.
• Adhere to all safety guidelines, SOPs, and regulatory requirements while performing testing and handling hazardous materials.

• Associate degree in a scientific discipline or equivalent experience;
  Bachelor’s degree preferred.
• 1‑3 years of experience in a laboratory or sample management role.
• Familiarity with LIMS or other sample tracking systems is 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.

Aequor Technologies