Senior Quality Engineer – Regulatory & Global Ops

Par Health; United States; On-site; USD 80,000 - 100,000; Full time

Job summary

Par Health is seeking a Sr. Quality Engineer to ensure compliance with quality systems and regulatory requirements in a cGMP manufacturing setting. The role involves providing statistical support, leading internal audits, and fostering continuous improvement initiatives. Candidates must possess a B.S. in Engineering or Science and at least 5 years of experience in a pharmaceutical environment. Strong communication and project management skills are essential. The position is based in the United States and offers opportunities for professional development.

Qualifications

• Minimum of 5 years of experience in QA/pharmaceutical manufacturing environment.
• Knowledge of SPC, DOE, FMEA, Six Sigma and Lean Manufacturing.
• Ability to manage multiple projects.

Responsibilities

• Provide guidance for regulatory filings and internal audits.
• Lead compliance efforts and continuous improvement activities.
• Conduct statistical analysis and implement corrective actions.

Skills

Statistical analysis

Process control

Team building

Project management

Communication skills

Education

B.S. degree in Engineering or Science

Tools

Mini-tab

Excel

Job description

Par Health is seeking a Sr. Quality Engineer to ensure compliance with quality systems and regulatory requirements in a cGMP manufacturing setting. The role involves providing statistical support, leading internal audits, and fostering continuous improvement initiatives. Candidates must possess a B.S. in Engineering or Science and at least 5 years of experience in a pharmaceutical environment. Strong communication and project management skills are essential. The position is based in the United States and offers opportunities for professional development.