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QC Lab Supervisor

Job

PrideStaff

Jupiter, FL (In Person)

$78,520 Salary, Full-Time

Posted 2 weeks ago (Updated 1 day ago) • Actively hiring

Expires 8/4/2026

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Job Description

Ready to Lead and Inspire in a Cutting-Edge Lab Environment? PrideStaff is recruiting on behalf of our client, a premier, fast-growing Contract Development and Manufacturing Organization (CDMO) . We are seeking a highly analytical, detail-oriented, and dynamic Quality Control Lab Supervisor to oversee daily laboratory operations and champion compliance. If you are a strong scientific problem-solver with a passion for mentoring talent, driving data integrity, and ensuring regulatory excellence, this leadership role is your next major career milestone! ##
Position Overview Job Title:
Quality Control Lab Supervisor Department:
Quality Control Reports To:
QC Manager Employment Type:
Full-Time, Exempt Work Arrangement:
Fully On-site Team Size:
Supervises 5-6 laboratory personnel ## Why This Role Matters As the QC Lab Supervisor, you are the linchpin of laboratory compliance and operational efficiency. You will provide critical technical leadership to a team of 5-6 personnel, ensuring the timely and accurate execution of analytical, microbiological, and in-process testing. Your expertise will directly support product release, stability programs, and validation activities in strict compliance with 21 CFR Part 211 and 21 CFR Part 507 . This is an impactful role where you can drive continuous improvement, lead sophisticated root cause investigations, and foster a culture of exceptional data integrity. ##
Key Responsibilities Team Leadership & Operations:
Supervise daily QC lab operations, manage resource planning, prioritize workloads, and handle personnel actions (interviewing, hiring, training, performance appraisals, and scheduling).
Data Review & Compliance:
Review and approve laboratory documentation, test records, methods, and protocols to ensure absolute compliance with cGMP, GDP, and data integrity expectations.
Investigation Leadership:
Lead and technical-review laboratory investigations, deviations, and non-conformances (OOS/OOT) using structured, scientific root-cause analysis methodologies.
Method & Lifecycle Support:
Oversee method development, validation, and enhancement activities. Coordinate the site's Stability Program, including sample management, pull schedules, and summary reporting.
Equipment & Readiness:
Ensure all GMP testing equipment (HPLC, TOC, Viscometers, etc.) remains qualified, calibrated, and maintained. Support internal, client, and FDA regulatory audits.
Cross-Functional Collaboration:
Partner closely with QA, Production, Engineering, and Supply Chain to support seamless site operations and quality initiatives. ## What You Bring to the
Table Education & Experience:
Degree:
BS in Chemistry, Microbiology, or a related scientific field (or equivalent hands-on experience).
Leadership Capabilities:
Proven ability to lead, instruct, and develop a small group of laboratory professionals.
Technical Expertise:
Hands-on experience with HPLC analysis , microbial sampling, and testing techniques.
Software Savvy:
Proficiency with Chromatographic Data Acquisition software— Empower experience is highly preferred.
Technical Knowledge & Skills:
Strong understanding of USP compendial and AOAC methods, as well as FDA and OSHA regulations. Deep knowledge of laboratory equipment (HPLC, analytical scales, viscometers, moisture analyzers, pH meters, TOC, and incubators). Advanced scientific troubleshooting and data calculation skills as they relate to formulations and chemical concentrations. Excellent written and verbal communication skills in English.
Computer & Systems Literacy:
Microsoft Office Suite (Word, Excel, PowerPoint, Outlook, Teams) and SharePoint.
Preferred experience:
ERP Systems (SAP), Electronic Quality Management Systems ( eQMS on the Salesforce platform preferred), and payroll systems (ADP). ##
Physical Demands & Work Environment Schedule:
Ability to work flexible hours, including days, evenings, weekends, holidays, and overtime as needed to respond to production demands.
Environment:
Fully on-site lab setting with occasional exposure to humidity, noise, and odors.
Physical:
Ability to stand, walk, or sit for extended periods; normal visual acuity required; willingness to wear full PPE (gloves, masks, goggles, gowns). ## Ready to Apply? If you are an experienced chemist or microbiologist ready to step into a rewarding leadership role with a premier CDMO, we want to hear from you. Apply today through PrideStaff and take the lead in your career!
Compensation / Pay
Rate (Up to): $37.00 - $38.50 Per Hour