QC Stability Sample Management.

Aequor; Holly Springs (NC); On-site; USD 65,000 - 90,000; Full time

Job summary

Aequor is seeking a Quality Control Senior Associate for an onsite role in Holly Springs, NC. The 12-month contract requires a 4/10 schedule (Wed–Sat, 7:30am–6:00pm) and full onsite work.

You will support QC Sample Management and Stability, handling samples, maintaining documentation, and ensuring regulatory compliance and GDP/GMP standards. Collaborate with lab analysts, QA, and cross-functional teams to maintain efficient testing workflows while driving continuous improvement and strict safety

Qualifications

• 3–5 years in a laboratory or sample management role.
• Familiarity with LIMS or other sample tracking systems.
• Strong attention to detail and teamwork.

Responsibilities

• Maintain chain of custody for incoming samples in the LIMS.
• Ensure labeling, storage and chain-of-custody documentation.
• Record data, assess results for specifications and GDP/GMP compliance.
• Troubleshoot issues and collaborate with senior staff on complex problems.
• Support investigations and audits with documentation.
• Collaborate with QC analysts and cross-functional teams to meet milestones.
• Suggest process improvements and contribute to QC efficiency.
• Adhere to safety guidelines and regulatory requirements during testing.

Skills

GMP QC experience

Sample management

Team player

Tools

LIMS

Job description

Title: Quality Control Senior Associate (Onsite Job in Holly Springs NC)

Location: Holly Springs NC - 27540

Terms: Contract W2 Only

Duration: 12 Months Contract assignment (with possible extension)

Candidate musts be available to work on a 4/10 (7:30am - 6pm), Wednesday through Saturday, schedule.

Description:

Fully Onsite

Candidate musts be available to work on a 4/10 (7:30am - 6pm), Wednesday through Saturday, schedule.

Job Summary:

The Quality Control Sr. Associate supports QC Sample Management and Stability team within the QC Support organization. The Sr. Associate will be 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 Sr. Associate will collaborate closely with laboratory analysts, Quality Assurance, and other cross-functional teams to maintain efficient and accurate testing workflows.

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 elevate 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.
• Compliance and Safety: Adhere to all safety guidelines, SOPs, and regulatory requirements while performing testing and handling hazardous materials.

Qualifications:

• 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.
• Available to work on a 4/10 schedule (7:30am - 6pm), Wednesday through Saturday, schedule.

Top 3 Must Have Skill Sets:

• GMP experience either in QC or manufacturing operations.
• Have worked in sample management or have sample management experience related to QC and/or manufacturing
• Team player and eager to learn and collaborate