QA Supervisor - Sterile Pharmaceutical Manufacturing

Wedgewood Pharmacy; San Jose (CA); On-site; USD 104,000 - 127,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

401(k) retirement plan

Company paid life and disability

Job summary

Wedgewood Pharmacy in San Jose, CA, is seeking a hands-on Quality Assurance Supervisor to lead QA activities in a sterile pharmaceutical manufacturing environment. You will approve materials, investigate deviations, and drive continuous improvement while mentoring QA Technicians and coordinating with Quality Control, Validation, and Production teams.

The role emphasizes strong cGMP knowledge, compliant documentation, and proactive problem solving.

Qualifications

• 2–3 years of experience with state and federal regulations and cGMP standards.
• Experience in a commercial compounding outsourcing or pharmaceutical facility preferred.
• Strong knowledge of quality systems, validation, CAPA, and document control.

Responsibilities

• Lead day-to-day QA activities in a sterile pharmaceutical manufacturing facility.
• Approve or reject materials and finished products against specifications.
• Perform investigations with root-cause analysis and corrective actions.
• Review protocols and reports for commissioning, maintenance, and validation of facilities and equipment.
• Mentor QA Technicians and lead a team to meet department goals.

Skills

Quality leadership

cGMP knowledge

Audits & CAPA

Documentation accuracy

Team mentoring

Tools

Microsoft Office

Data-entry systems

Job description

Wedgewood Pharmacy in San Jose, CA, is seeking a hands-on Quality Assurance Supervisor to lead QA activities in a sterile pharmaceutical manufacturing environment. You will approve materials, investigate deviations, and drive continuous improvement while mentoring QA Technicians and coordinating with Quality Control, Validation, and Production teams.

The role emphasizes strong cGMP knowledge, compliant documentation, and proactive problem solving.