Quality Project Manager

Nemera•Buffalo Grove, IL

41d•$120,000 - $135,000

About The Position

KEY RESPONSIBILITIES/ESSENTIAL FUNCTIONS: Assists Associate Director of Quality in coordinating and executing goals and objectives throughout the company to improve product quality and operating system efficiency. Direct and coordinate the activities of Quality Department employees. Establish and maintain sound relationships with production, technology, supply chain, quality teams and cross functional personnel to identify system and compliance gaps with proposed resolutions. Act as liaison with metrology, QC and compliance team Ensure adherence to project and company standards, while maintaining quality systems that meet customer, internal, and regulatory requirements (ISO, cGMP, FDA, Health & Safety). Manage claims non-conformities, investigations, problem solving, root cause analysis, champion creation of effective and sustainable corrective actions. Manage process and equipment Validations for new product and existing business. Change control process owner Define and implement quality initiatives to meet KPI’s and objectives. Identify opportunities for improvement through data trending and analysis, as well as develop and implement quality and inspection processes. Engage in risk assessment process; data integrity, control and management utilizing risk assessment tools such as FMEA. Review and approve technical protocols, reports, and specifications, as appropriate. Participate and lead CAPA activities as required, utilizing problem solving techniques to reduce internal and external failures. Employ necessary tools/resources and perspectives, treating all co-workers with respect/dignity and valuing feedback. Responsible for the coordination and evaluation of the Quality department. Supervises staff in line with company policies and laws, including hiring, training, task management, performance evaluation, discipline, and conflict resolution. Make hiring decisions for their direct reports. Represent the Quality Department in support of customer, ISO and third-party audits. Other duties as assigned

Requirements

Bachelor’s degree in Engineering or related field
4+ years of relevant working experience in Quality in a manufacturing environment with 1+ year experience in a supervisory role
Excellent communication skill with the ability to understand, read, write, and speak English
Ability to apply advanced mathematical concepts and intermediate statistical (SPC) knowledge
Strong understanding of injection molding, Automation and FMEA.
Knowledgeable to equipment/process/product validation practices and principles.
Excellent interpersonal, organizational and communication skills.
Demonstrated leadership and the ability to motivate and influence others.
Able to lift up to 30 lbs.
Ability to push and pull items
Ability to sit, stand, walk 80% of shift required

Nice To Haves

Self-directed and possess knowledge of business and management principles involved in strategic planning, resource allocation and coordination of people and resources.
Knowledge of inspection tools, including their design, use, repair and maintenance
Medical device and/or Pharmaceutical Industry experience preferred
Six sigma training and/or certifications preferred.
Demonstrated organizational skills and general knowledge of PC applications such as Microsoft Word, Excel and Database software such as SAP

Responsibilities

Assists Associate Director of Quality in coordinating and executing goals and objectives throughout the company to improve product quality and operating system efficiency.
Direct and coordinate the activities of Quality Department employees.
Establish and maintain sound relationships with production, technology, supply chain, quality teams and cross functional personnel to identify system and compliance gaps with proposed resolutions.
Act as liaison with metrology, QC and compliance team
Ensure adherence to project and company standards, while maintaining quality systems that meet customer, internal, and regulatory requirements (ISO, cGMP, FDA, Health & Safety).
Manage claims non-conformities, investigations, problem solving, root cause analysis, champion creation of effective and sustainable corrective actions.
Manage process and equipment Validations for new product and existing business.
Change control process owner
Define and implement quality initiatives to meet KPI’s and objectives.
Identify opportunities for improvement through data trending and analysis, as well as develop and implement quality and inspection processes. Engage in risk assessment process; data integrity, control and management utilizing risk assessment tools such as FMEA.
Review and approve technical protocols, reports, and specifications, as appropriate.
Participate and lead CAPA activities as required, utilizing problem solving techniques to reduce internal and external failures.
Employ necessary tools/resources and perspectives, treating all co-workers with respect/dignity and valuing feedback.
Responsible for the coordination and evaluation of the Quality department.
Supervises staff in line with company policies and laws, including hiring, training, task management, performance evaluation, discipline, and conflict resolution.
Make hiring decisions for their direct reports.
Represent the Quality Department in support of customer, ISO and third-party audits.
Other duties as assigned