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Associate Quality Control
Contract: Holly Springs, North Carolina, US span>
Salary Range: 30.00 - 33.00 | Per Hour
Job Code: 369371
End Date: 2026-05-17
Job Status: Expired
This Job is no longer accepting applications
Title: Associate Quality Control
Location: Holly Springs NC
Duration: 1 year
- We are seeking a highly motivated and experienced Associate in Quality Control (QC) Chemistry to support the startup and operational readiness of our QC laboratory.
- Working with minimal supervision, this individual will lead and contribute to critical activities including system qualifications, method transfers, and laboratory operations in a GMP-regulated environment.
- Collaborate cross-functionally with site teams to implement work order and preventative maintenance systems for laboratory equipment.
- Review and contribute to validation documentation to support onboarding of equipment and computerized systems.
- Draft, revise, and review technical and quality documentation such as SOPs, test methods, technical assessments, validation reports, trend reports, and safety evaluations.
- Assist in the procurement of laboratory consumables and critical reagents required for startup activities.
- Coordinate and execute training and method transfer activities for instruments including H/UPLC, TOC, Conductivity, Osmolality and other chemistry-based platforms.
- Actively participate in audits, quality initiatives, and cross-functional projects with site or global impact.
- Provide routine operational support during weekends and public holidays as required.
- Bachelor's degree or higher in Chemistry, Compendial testing or a related scientific discipline.
- Minimum of 4 years of relevant laboratory experience in a GMP pharmaceutical or biopharmaceutical manufacturing environment, with a strong background in analytical testing.
- Proficient in analytical laboratory techniques and instrumentation.
- Experience with pharmacopeias is preferred.
- Familiarity with laboratory systems such as LIMS and LMES/CIMS.
- Demonstrated understanding of industry regulations, data integrity, and compliance standards.
- Strong technical writing, documentation, and communication skills.
- Experience with method validation, verification, and transfer.
- Excellent interpersonal skills with the ability to collaborate across teams and adapt to varying communication styles.
- Must have a chemistry background
- GMP experience
- Empower experience
Job Requirement
- Empower
- GMP experience
- LIMS
Reach Out to a Recruiter
- Recruiter
- Phone
- sakshi malviya
- sakshi.malviya@collabera.com