Job Market Guide: Director of Quality jobs in Harrisburg-Lancaster-Lebanon-York

Competition
High
0.726622
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Director of Qualitys in Harrisburg-Lancaster-Lebanon-York. Director of Qualitys in Harrisburg-Lancaster-Lebanon-York have between ${} and ${} years of experience, averaging $${} years of experience.

31 Director of Quality jobs in Harrisburg-Lancaster-Lebanon-York

West Point, PA
This position will be responsible for ensuring appropriate stability guidance is provided for all new biologic programs at the Formal Stability Study stage to develop a solid stability package for filing worldwide.
industry
Biotech/Pharma
experience
5 - 7 years

Alexandria, VA
In this role, the selected candidate will be responsible for quality, risk, regulatory compliance, and education within an organization large enough to provide adequate support and infrastructure, but still small enough for an individual employee to make a large contribution to the enterprise.
industry
Patient Care
experience
Less than 5 years

West Point, PA
The Director, West Point Quality Systems, reports to the Director, West Point Quality Assurance, and supports all Quality Assurance and GMP compliance activities relating to the manufacture of pharmaceutical and vaccine products to ensure compliance with all applicable regulations and specifications.
industry
Biotech/Pharma
experience
8 - 10 years

Lansdale, PA
In this role, you will engage with external quality stakeholders in a balanced and credible manner consistent with the regulatory environment and companys ethical standards.
industry
Biotech/Pharma
experience
5 - 7 years

Baltimore, MD
In this role, you will collaborate with appropriate staff, disciplines, and departments in developing and overseeing the implementation of plans of corrective action once opportunities for improvement are identified.
industry
Healthcare IT
experience
5 - 7 years

West Point, PA
In this role, the selected candidate will be responsible for ensuring appropriate stability guidance is provided for all new biologic programs at the Formal Stability Study stage to develop a solid stability package for filing worldwide.
industry
Biotech/Pharma
experience
5 - 7 years

Wilmington, DE
This position is responsible for planning, managing and executing medical device product development; this includes the coordination of activities involving multiple parties while providing leadership to the team.
industry
Medical Devices & Diagnostics
experience
11 - 15 years

Philadelphia, PA
In this role, you will collaborate with quality leadership and other key stakeholders to formulate and establish policies, operating procedures, and goals in compliance with internal and external guidelines.
industry
Healthcare IT
experience
8 - 10 years

Morgantown, PA
The Quality Director is responsible for administering the company quality program in accordance with customer and company requirements.
industry
Automotive
experience
8 - 10 years

West Chester, PA
This position is responsible for planning, managing and executing medical device product development; this includes the coordination of activities involving multiple parties while providing leadership to the team.
industry
Medical Devices & Diagnostics
experience
11 - 15 years

Pennsauken, NJ
In this role, you will process improvement, analysis of information, strategic planning, verbal and written communication, quality engineering, emphasis on excellence and thoroughness, dealing with complexity.
industry
Consumer Goods / Miscellaneous
experience
8 - 10 years

West Point, PA
In this role, you will be responsible to provide strategic decision making and executive sponsorship of quality initiatives in the area of biologics and therapeutic proteins analytical testing
industry
Biotech/Pharma
experience
8 - 10 years

Washington, DC
In this role, the selected candidate will be responsible for quality, risk, regulatory compliance, and education within an organization large enough to provide adequate support and infrastructure, but still small enough for an individual employee to make a large contribution to the enterprise.
industry
Patient Care
experience
Less than 5 years

Baltimore, MD
This position is responsible for planning, managing and executing medical device product development; this includes the coordination of activities involving multiple parties while providing leadership to the team.
industry
Medical Devices & Diagnostics
experience
11 - 15 years

Havre De Grace, MD
This position is responsible for planning, managing and executing medical device product development; this includes the coordination of activities involving multiple parties while providing leadership to the team.
industry
Medical Devices & Diagnostics
experience
11 - 15 years

Philadelphia, PA
In this position, you will develop and lead complex interdepartmental and multi-entity performance improvement projects that address identified gaps in performance or aspirations for higher levels of outcomes.
industry
Biotech/Pharma
experience
Less than 5 years

Arlington, VA
In this role, the selected candidate will be responsible for quality, risk, regulatory compliance, and education within an organization large enough to provide adequate support and infrastructure, but still small enough for an individual employee to make a large contribution to the enterprise.
industry
Patient Care
experience
Less than 5 years

West Point, PA
The Director, West Point Quality Systems, reports to the Director, West Point Quality Assurance, and has a dotted line reporting structure to the Executive Director, West Point Site Quality. This position supports all activities to realize key deliverables of the Quality System Improvement Program (QSIP), Quality Management System (QMS) installation and Quality Risk Management (QRM) deployment at the West Point Site.
industry
Biotech/Pharma
experience
8 - 10 years

Frederick, MD
In this role, the selected candidate will provide leadership, direction, and mentoring to ensure that the QC organization is successful in meeting the quality and manufacturing objectives in support of corporate goals.
industry
Biotech/Pharma
experience
15+ years

Arlington, VA
In this role, you will conduct Practice Site (pharmacies, health system organizations, physician practices) visits to understand and document clinical workflow implications and value of Surescripts product offerings.
industry
Market Research
experience
Less than 5 years