Quality Control Supervisor

Afton Scientific, LLC•Charlottesville, VA

46d•Onsite

About The Position

At Afton Scientific, every role contributes to advancing the quality and reliability of sterile pharmaceutical manufacturing. Our team is driven by innovation, collaboration, and a commitment to excellence. We support employees at every stage of their career by fostering an environment where development, learning, and meaningful impact are possible. We invite you to explore opportunities to join our organization and contribute to our mission. We are currently seeking a Quality Control Supervisor to support our growing biopharmaceutical operations at our on-site facility in Charlottesville, Virginia. Overview of this Position: The QC Analytical Chemistry Supervisor is responsible for the oversight, performance, and continuous improvement of analytical testing in support of pharmaceutical manufacturing operations. This role supervises daily QC laboratory activities, supports analytical staff, ensures adherence to pharmacopeial and regulatory requirements, and provides technical guidance on method execution, data integrity, and laboratory compliance. This position also contributes to method development and qualification, oversees laboratory instrumentation and maintenance schedules, participates in audits, and ensures accurate review and documentation of laboratory operations in alignment with FDA, ICH, USP, EU, and related quality expectations.

Requirements

Bachelor’s degree in chemistry or a closely related scientific discipline
Minimum 5 years of experience in pharmaceutical analytical testing in a cGMP environment, including hands‑on operation of HPLC, GC, FTIR, KFT, UV‑Vis, and similar technologies
Demonstrated experience in regulated laboratory settings (FDA/ICH/USP), including strong understanding of data integrity (ALCOA+) and cGMP compliance
Proficiency in reviewing and approving laboratory documentation (SOPs, deviations, OOS/OOT/OOE/NCMR, protocols, reports)
Strong background in chromatography and experience using Empower
Experience with raw material testing, stability testing, and LIMS
Strong written and verbal communication skills

Nice To Haves

Experience supervising or mentoring laboratory personnel
Experience supporting regulatory or client audits
Strong technical troubleshooting abilities with analytical methods or laboratory equipment

Responsibilities

Develop, implement, and maintain HR policies and procedures to support organizational compliance
Supervise daily QC Analytical Chemistry Laboratory operations related to production support, testing activities, and staff oversight
Provide guidance to laboratory staff and assist in the management and development of QC analytical personnel as directed by the QC Manager
Execute and oversee cGMP‑compliant analysis of raw materials, APIs, and pharmaceutical finished products using pharmacopeial and regulatory methods (USP, NF, JP, EU, FDA, ICH)
Ensure proper design, execution, documentation, and validation of analytical techniques, instrumentation, and test methods used in the laboratory
Review executed laboratory operations for accuracy, completeness, and compliance with internal SOPs and external regulatory expectations
Oversee equipment calibrations, verifications, and preventative maintenance activities for laboratory instrumentation and supporting equipment
Identify technical issues and lead independent troubleshooting efforts, providing follow‑up and solutions to management as needed
Participate in client and regulatory audits as a QC representative and maintain professional, prepared communication with external partners and internal teams
Write, review, or approve SOPs, validation protocols, specifications, and investigation reports as applicable (e.g., OOS, OOT, ODR, NCMR)
Assist with procurement of laboratory equipment and supplies and contribute to process improvements within the QC laboratory