Quality Control Technician in a Manufacturing Environment

Requirements

• Environmental monitoring experience.
• Quality inspection experience.
• Batch record review experience.
• Pharmaceutical, medical device, veterinary, or food manufacturing experience.

Benefits

Additional Information

At Wedgewood Pharmacy, we are dedicated to improving the lives of animals through customized medication and compassionate care. Every role in our organization contributes to helping pets live healthier, happier lives. We are a team driven by purpose, quality, and a shared commitment to animal health. The Quality Control Technician supports product quality and regulatory compliance through environmental monitoring, inspection, sampling, contemporaneous batch record review, and in-process quality verification activities in a sterile pharmaceutical manufacturing facility. The role serves as the first line of quality verification within manufacturing operations and is responsible for identifying and escalating quality concerns in a timely manner. When will you work? The hours for this position are Monday - Friday 8:00am-4:30pm. What you'll do- Essential Responsibilities: Perform environmental monitoring activities including viable air sampling, surface sampling, personnel monitoring, and associated documentation according to approved procedures. Monitor storage conditions of the manufacturing environment, materials, and products. Prepare, package, and ship environmental monitoring and product samples to external contract laboratories. Review and retain all records associated with batch issuance, work instructions, release of product and all quality management data. Perform incoming material, component, packaging, and labeling inspections. Conduct in-process and finished product inspections. Perform contemporaneous review of batch production records during formulation, filtration, filling, inspection, packaging, labeling, and related manufacturing operations. Verify calculations, material identification, equipment status, line clearance activities, and production documentation. Review manufacturing records for completeness, legibility, and compliance with Good Documentation Practices (GDP) and Data Integrity. Monitor manufacturing and storage environmental conditions and report abnormalities. Maintain retain sample inventories and associated records. Assist with environmental monitoring excursions, investigations, and quality event documentation. Generate routine quality data and support trend analysis activities. Participate in inspections, audits, and continuous improvement initiatives. Who you are (Knowledge, Skills and Abilities): Strong communication skills Ability to adapt to changing priorities and circumstances Ability to identify and escalate quality concerns Ability to work in a dynamic, fast-paced and timeline-driven environment with shifting priorities Strong attention to detail Strong understanding of Microsoft Office and Excel software Good Documentation Practices (GDP) Ability to follow written procedures Basic mathematical and calculation skills What you've done: Minimum one year experience in manufacturing, laboratory, quality, food, pharmaceutical, veterinary, medical device, healthcare, or other regulated environment preferred. High School Diploma or GED required.

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