Wedgewood Pharmacy
Pharma
QualityControlTechnician
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Quality Control Technician at Wedgewood Pharmacy. Skills: Quality control, Manufacturing operations, Regulatory compliance. Perform environmental monitoring. Monitor storage conditions”
Industry & Context.
Identify quality concerns
What They're Looking For.
Must Have
High School Diploma or GED required, One year experience in regulated environment preferred
Nice to Have
Environmental monitoring experience, Quality inspection experience, Batch record review experience, Pharmaceutical manufacturing experience, Medical device manufacturing experience, Veterinary manufacturing experience, Food manufacturing experience
What You'll Do.
Perform environmental monitoring
Monitor storage conditions
Prepare samples for shipping
Review and retain records
Perform incoming material inspections
Perform component inspections
Perform packaging inspections
Perform labeling inspections
Conduct in-process inspections
Conduct finished product inspections
Perform batch record review
Verify material identification
Verify equipment status
Verify line clearance
Verify production documentation
Review manufacturing records
Monitor manufacturing environmental conditions
Monitor storage environmental conditions
Maintain retain sample inventories
Assist with investigations
Document quality events
Generate quality data
Support trend analysis
Participate in inspections
Participate in audits
Participate in continuous improvement
How You'll Work.
Team & Collaboration
Cross-functional coordination; Vendor management; Stakeholder management
Communication Scope
Escalate quality concerns
Full Job Description
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 an
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