QA Supervisor

QA Supervisor

DRx a division of Purkinje is currently seeking a Quality Assurance Supervisor for our facility in Skokie, Illinois.

Responsibilities
Schedules and follows up on the results of all analytical QC testing by coordinating the needs of production, technical services, customer complaints and regulatory commitments.
Maintains the sample log and/or database.
Reviews documentation for thoroughness, clarity and compliance to all internal and external requirements.
Based on the review, the supervisor assigns a disposition to the samples.
Performs detailed OOS investigations to determine reasons for product deviations.
Hires and trains new personnel.
Evaluates personnel performance and discusses expectations with their direct reports periodically.
Keeps SOPs updated as well as keeping the lab personnel trained on changes in procedures.
Assists with drafting, reviewing and approving laboratory SOPs.
Performs daily, weekly and monthly audits and submits reports to manager. Participates in new product project teams.
Assists in preparing written reports for special projects, responses to regulatory agencies, and internal and external audits.
Assists with reviewing and approving change controls and protocols.
Evaluates and recommends new equipment purchases for the laboratory.
Maintains expenses at or below budget.

Company Information:
For more than 15 years, DRx has been a trusted supplier of pre-packaged prescription medications, OTC products and related supplies to physician offices and clinics throughout the United States. DRx is a fully licensed, FDA registered facility and ships nationwide from its repackaging facility in Skokie, Illinois.

In 2000, DRx was acquired by Purkinje, a developer of diagnosis-driven prescribing software. Purkinje technology allows customers to streamline the dispensing process and automate inventory, reporting, and compliance functions, reducing overhead and improving profitability. With over 120 employees and offices in the US, Canada, and India, Purkinje continues to develop breakthrough solutions for clinical documentation, care management, electronic prescribing and medication dispensing.
REQUIREMENTS
Bachelor's degree or equivalent experience in QA
Previous experience developing quality assurance processes and procedures in accordance to regulations
Proficient in Microsoft Office suite of software
Strong interpersonal capabilities along with solid verbal and written communication skills, and strong attention to detail, organization, decision-making, and self-administrative skills required.
Ability to lead, motivate and develop a team of individuals