Quality Control Supervisor - Chemistry

Eagle Labs, Inc•Seminole, FL

22h•$85,000 - $87,000

About The Position

Quality Control (QC) Chemistry Supervisor oversees the daily testing of raw materials, in-process samples, finished products and stability. In addition, they oversee the daily operations of the analytical chemistry laboratory. They lead teams of QC analysts, ensure adherence to cGMP guidelines, and manage laboratory compliance, investigations, and instrumentation to guarantee product safety and regulatory approval.

Requirements

A Bachelor's degree or higher in Chemistry, Biochemistry, or a closely related scientific discipline.
Minimum –5 years of relevant pharmaceutical QC experience, with at least 3 or more years in a direct supervisory or leadership role.
Deep understanding of cGMP, FDA regulations, and pharmacopeial standards (e.g., USP, EP).
Strong problem-solving, data trending capabilities, and excellent verbal and written communication skills.
Proficiency in advanced laboratory software (e.g., LIMS, Empower)

Responsibilities

Supervise, train, and mentor QC analysts. Manage scheduling, performance evaluations, and daily workload distribution to meet production timelines
Managing a team of analysts, ensuring compliance with cGMP/GLP, reviewing test data, investigating out-of-specification (OOS) results, and managing stability programs and method validations
Enforce strict laboratory safety standards and maintain compliance with chemical hygiene plans
Ensure that critical analytical instruments (e.g., HPLC, GC, FTIR, UV-Vis) are routinely calibrated, maintained, and verified for compliance.
Ensure Data Integrity
Act as a subject matter expert (SME) during internal audits and regulatory inspections.
Manage daily lab workflows, scheduling, and workload distribution.
Oversee training, performance evaluations, and mentorship for QC chemistry analysts.
Ensure routine and non-routine chemical assays are performed accurately.
Review and approve analytical data generated from techniques like HPLC, GC, dissolution, and wet chemistry.
Spearhead investigations into Out-of-Specification (OOS) and Out-of-Trend (OOT) results.
Author, revise, and approve Standard Operating Procedures (SOPs), protocols, and technical reports.
Participate in internal and regulatory facility audits (e.g., FDA inspections) and ensure the laboratory remains audit-ready at all time
Maintain an audit-ready laboratory environment.
Ensure analytical instruments are calibrated, maintained, and validated according to strict regulatory standards.