Quality Engineer: Onsite Pharma QA & Lean Six Sigma

West Pharmaceutical Services, Inc; Jersey Shore (Lycoming County); Hybrid; USD 85,000 - 110,000; Full time

Benefits offered by this job

PTO

Inclusive culture

Community involvement

Onsite work environment

Job summary

West Pharmaceutical Services, Inc. in Jersey Shore, PA seeks a Quality Engineer to join our QA/QC team. You will be hands-on in measuring and analyzing data, implementing corrective actions, and driving continuous improvement in production and QC areas.

This onsite role requires 5 days on site per week with no relocation. A Bachelor's in Engineering/Biology/Business and 3+ years in a regulated pharma/medical device setting are preferred, along with Lean Six Sigma knowledge.

Qualifications

• Bachelor's Degree in Engineering, Biology, or Business or equivalent experience.
• Minimum 3 years in a Quality or Engineering role at a regulated manufacturer.
• Knowledge of Lean, Six Sigma, DMAIC, PDCA, and root cause analysis.

Responsibilities

• Drive improvement of site and departmental goals and cost of quality.
• Provide quality reports and review trends for areas of responsibility.
• Perform root cause analysis and implement corrective actions.
• Support Lean Six Sigma programs toward targets and continuous improvement.
• Participate in risk/hazard analysis for products and processes.
• Conduct quality shop floor audits and support measurement systems.
• Assist with QA/QC, process engineering, and production initiatives.

Skills

Problem solving

Root cause analysis

Data analysis

Lean Six Sigma

Quality mindset

Education

Bachelor's Degree in Engineering, Biology, or Business

Tools

Minitab

CMMs/CNC

SAP ERP

Job description

West Pharmaceutical Services, Inc. in Jersey Shore, PA seeks a Quality Engineer to join our QA/QC team. You will be hands-on in measuring and analyzing data, implementing corrective actions, and driving continuous improvement in production and QC areas.

This onsite role requires 5 days on site per week with no relocation. A Bachelor's in Engineering/Biology/Business and 3+ years in a regulated pharma/medical device setting are preferred, along with Lean Six Sigma knowledge.