Quality Engineer

Ingersoll Rand is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.

Ingersoll Rand is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.

Job Summary:

The PharmBio business quality engineer actively supports on-site pharmaceutical containment manufacturing on a day-to-day basis.  The quality engineer would utilize their knowledge of ILC Dover quality systems to drive compliance to ILC Dover, ISO 9001, ISO 13485, and customer standards. As part of these actions, they will identify continuous improvement opportunities and participate in team activities that drives these opportunities to closure. The quality engineer may also participate in customer facing interactions such as audits, and customer complaint responses.

Successful candidates will have cGMP experience in pharmaceutical and/or medical device manufacturing environments, a data driven approach, and a willingness to work together as a team.

Essential Job Responsibilities:

• Design and implement audits and control plans for products to ensure product quality targets are met.
• Establish, define, implement, maintain, and report on quality assurance key performance measures and standards.
• Investigate non-conformances and consumer complaints, lead completion of root cause analysis, implement corrective actions, and monitor progress and improvements.
• Drive continuous improvement on quality standards, requirements, and best practices.
• Create and maintain quality systems documentation, such as quality manuals, procedures, and work instructions. 
• Devises sampling procedures and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data.
• Applies statistical process control (SPC) methods for analyzing data to evaluate the current process and process changes.
• Prepares and presents technical and program information to team members and management.
• Directs technical and administrative workers engaged in quality activities.
• Maintains a working knowledge of government and industry quality codes and standards including ISO 9001 and ISO13485.

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Other duties, responsibilities and activities may change or be assigned at any time with or without notice.

Basic Qualifications:

• Bachelor of Engineering (BE) or Bachelor of Science in Engineering degree (BSE) or an equivalent number of relevant years of experi