Strategic Pharma Operations & Quality Engineer

Skills Alliance; Indiana (PA); On-site; USD 100,000 - 130,000; Full time

Job summary

A leading healthcare consulting firm is seeking an Associate Director I Therapeutics to manage quality assurance initiatives and ensure compliance with regulations. The role requires a Bachelor's degree in Life Sciences or Engineering, with a preference for candidates with experience in a regulated manufacturing environment. Strong project management and problem-solving skills are essential. This is a full-time position based in Indiana.

Qualifications

• Minimum of 2 years of relevant experience in a regulated manufacturing environment.
• Strong understanding of applicable regulatory guidelines and validation principles.
• Experience with statistical analysis tools; Lean or Six Sigma certification preferred.

Responsibilities

• Manage and track reliability-related improvement initiatives.
• Lead projects focused on reliability and process enhancement.
• Serve as the quality contact for risk management activities.

Skills

Regulatory compliance

Root cause analysis

Project management

Statistical analysis

Process improvement

Education

Bachelor’s degree in Life Sciences or Engineering

Tools

Microsoft Office

Quality engineering tools

Job description

A leading healthcare consulting firm is seeking an Associate Director I Therapeutics to manage quality assurance initiatives and ensure compliance with regulations. The role requires a Bachelor's degree in Life Sciences or Engineering, with a preference for candidates with experience in a regulated manufacturing environment. Strong project management and problem-solving skills are essential. This is a full-time position based in Indiana.