Aequor logo

Senior Quality Control Associate

Job Overview

moneybag

Compensation

Hourly
Range $16.75 - $28.00
clock

Work Schedule

Night Shifts
diamond

Benefits

Health Insurance
Dental Insurance
Paid Time Off
Retirement Plan
Contract work flexibility
Career development opportunities
onsite work

Job Description

Our client is a leading organization in the pharmaceutical and biotechnology industry, based in Holly Springs, North Carolina. The company is renowned for its commitment to innovation and quality in the development and manufacture of biologic products. It operates within stringent regulatory frameworks including GMP (Good Manufacturing Practices) and adheres to high standards to ensure product safety and efficacy. The organization values expertise in quality control and quality assurance as they play a critical role in the lifecycle of biologic products from research and development to commercial production. With a focus on employee development and maintaining a safe, compliant work environment, the company fosters growth and skill enhancement in the field of life sciences.

We are currently seeking a Night Shift Quality Control Senior Associate to join the team on a contract basis for 12 months, with the possibility of extension. This is a full-time contract role located onsite in Holly Springs, NC. The position requires working a night shift of 10 hours from Wednesday through Saturday, starting at 10 PM. Initially, the candidate will undergo training during the day shift before transitioning to nights. The key responsibility in this role is to enhance various laboratory systems that assure the safety and quality of biologic products through rigorous testing and compliance with established protocols.

This role is ideal for candidates with a Bachelor of Science degree in Chemistry, Microbiology, or any related scientific field who have solid experience working in a GMP-regulated laboratory environment. The ideal candidate will have practical knowledge of laboratory information management systems (LIMS) and hands-on experience with advanced laboratory techniques such as chromatography and bioassays. They will be experienced in handling quality control workflows, following SOPs (Standard Operating Procedures), and supporting audit processes within the pharmaceutical, biotech, or life sciences sectors.

The Night Shift Quality Control Senior Associate will be performing essential analytical and microbiological testing to ensure the compliance of biologic products with regulatory standards. This role demands keen attention to detail, strong organizational skills, and the ability to liaise effectively with multiple departments including QC, manufacturing, and laboratory teams. Furthermore, the candidate will be responsible for maintaining sample integrity, documenting all test results accurately in the LIMS system, and following stringent safety protocols to maintain a contamination-free workspace. This position provides an excellent opportunity for professionals seeking to advance their careers in quality control within a dynamic and highly regulated industry environment.

Job Requirements

  • Must have BS in Chemistry, Microbiology, or any Science field
  • experience working in GMP environment and laboratory
  • ability to work night shifts and flexibility to train during day shift
  • knowledge of laboratory information management systems
  • understanding of quality control and testing procedures
  • familiarity with SOPs and compliance requirements
  • strong attention to detail and safety awareness

Job Qualifications

  • Bachelor of Science degree in Chemistry, Microbiology, or related scientific field
  • experience working in GMP laboratory environment
  • hands-on experience with LIMS
  • knowledge of quality control testing workflows
  • experience with chromatography and bioassays
  • understanding of GMP or ISO-regulated environments
  • ability to support audit processes
  • excellent organizational and communication skills

Job Duties

  • Receive, inspect, and log samples
  • verify integrity and documentation
  • assign IDs in LIMS and prepare samples for testing (aliquoting, labeling, storage)
  • perform routine chemical analyses such as potency and purity using validated methods
  • execute cell-based bioassays and maintain culture integrity
  • perform PCR testing in microbiology
  • maintain storage areas per SOPs and monitor conditions
  • complete receipt/disposition forms ensuring GMP/SOP compliance and supporting audits
  • liaise with QC, manufacturing, and labs to manage pickups/deliveries and report issues
  • update sample data in LIMS and support process improvements and SOP reviews
  • follow safety protocols and keep areas organized
  • dispose of samples per procedures

Job Criteria

Experience

Expert Level (7+ years)


Job Location

Your Profile Is Visible To Hiring Managers Across OysterLink.

We'll match you with best jobs

Get job offers faster

Business woman
Business man
Search For More Opportunities:

How Candidates Get Hired Faster

Apply to 2–3 similar roles

Complete profile & get best matches

Check new opportunities daily

Woman chef
Man chef