Find & Apply For Quality Control Analyst Jobs in Woburn, Massachusetts

Title:

Quality Operations Specialist - 1st

Shift Location:

Woburn, MA 01801

Job Type:

Temp-to-Hire Schedule:

Monday-Friday, 6:00 AM-2:30

PM Pay Rate:

$23-$25/hour during the temporary assignment; $26/hour upon permanent conversion

Start Date:

ASAP Job Summary We are seeking a detail-oriented Quality Operations Specialist to support pharmaceutical manufacturing and repackaging operations. This role is responsible for quality inspections, label creation, documentation management, controlled substance tracking, and compliance with current Good Manufacturing Practices (cGMP) and FDA regulations. The ideal candidate will have pharmaceutical industry experience, a strong quality assurance background, excellent documentation skills, and the ability to work accurately in a regulated environment. Key Responsibilities Create, revise, and maintain pharmaceutical product labels and drug information in company systems. Perform incoming, in-process, and final quality inspections of pharmaceutical products and repackaging components. Review finished products, equipment, facilities, and production processes to ensure compliance with quality standards and cGMP requirements. Maintain training records, supplier lists, quality documentation, and electronic system records. Complete document filing and update records in the QAD system. Track controlled substance samples and maintain DEA Form 222 documentation and quarterly ARCOS reporting. Assist with deviation investigations, incident reports, and corrective documentation. Conduct quality audits, compile data, document findings, and communicate results to management. Perform daily and monthly controlled substance retain sample audits. Support scheduled and unscheduled destruction of prescription and over-the-counter medications. Contact manufacturers to obtain drug information and communicate with customers as needed. Promptly report quality concerns, inspection discrepancies, and out-of-specification results to management. Required Qualifications Bachelor's degree in a science-related field. Minimum of 3 years of experience in the pharmaceutical industry. Previous quality assurance or quality control experience in an FDA-regulated facility. Knowledge of pharmaceutical medication repackaging processes. Familiarity with cGMP requirements and quality documentation practices. Proficiency in Microsoft Word, Excel, PowerPoint, and SharePoint. Strong attention to detail, organizational skills, and written communication abilities. Ability to read, write, and communicate effectively in English. Ability to lift up to 30 pounds as needed and perform visual inspections, with corrective devices or supports as applicable. Reliable attendance and the ability to consistently meet the scheduled work hours. #

VMS Pay:

$23.00 - $25.00 per hour Expected hours: 40.0 per week

Benefits:

401(k) Dental insurance

Work Location:

In person