layiq

/la·yiq/adjective

worthy; deserving; fitting; suitable.

A role, opportunity, or path that merits attention, time, and pursuit.

Quality Assurance Supervisor in a Pharmaceutical Manufacturing Environment at Wedgewood Pharmacy | LAYIQ

Lead day-to-day Quality Assurance activities within a sterile pharmaceutical manufacturing facility, helping ensure our products consistently meet established standards for safety, identity, strength, quality, and purity. You will combine hands-on quality systems expertise with people leadership to strengthen compliance, solve problems, and drive continuous improvement across the site.
Approve or reject starting materials, packaging and labeling materials, intermediates, bulk products, and finished products against established specifications.
Perform, review, and approve quality investigations, ensuring appropriate root cause analysis, corrective actions, and product disposition.
Review and approve protocols and executed reports supporting commissioning, maintenance, and validation of facilities, processes, and equipment.
Ensure initial and continuing training requirements are completed and adapted based on team and business needs.
Create, revise, and approve controlled documents and process changes.
Compile and report monthly quality-system metrics, identify trends, and drive continuous improvement initiatives.
Participate in internal audits and risk assessments; monitor relevant industry trends and recommend improvements.
Lead and mentor a team of QA Technicians, setting clear expectations and ensuring department goals and deadlines are met.
Build a positive, accountable work environment through effective communication, coaching, performance management, and team development.
Partner closely with Quality Control, Validation, and Production on QMS changes, improvements, and routine cGMP activities.
Identify potential adverse quality issues early and help drive timely, compliant resolution.
Perform other duties as assigned to support appropriate quality practices across the site.
Who you are: A hands-on quality leader who can balance strong compliance standards with coaching, collaboration, and accountability.
Highly organized and detail-oriented, with excellent documentation skills and the ability to identify potential adverse quality issues.
A confident written and verbal communicator with strong presentation skills and the ability to work effectively across departments.
Knowledgeable in cGMP requirements, state and federal regulations, and quality-system best practices.
Proficient with Microsoft Office and data-entry systems, with the ability to compile, interpret, and clearly communicate quality metrics.

Quality Assurance Supervisor in a Pharmaceutical Manufacturing Environment

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