Job Market Guide: Director of Quality jobs in PA

Competition
Desired Skills
Years of Experience
Years of Experience distribution graph for Director of Qualitys in PA. Director of Qualitys in PA have between ${} and ${} years of experience, averaging $${} years of experience.

23 Director of Quality jobs in PA

$150K - $200K - Willow Grove, PA
The Quality Assurance Director Quality Systems is responsible for developing, revising and maintaining quality assurance systems to ensure compliance with cGMPs and contract vendor requirements in a pharmaceutical environment.
industry
Biotech/Pharma
experience
8 - 10 years

eCommerce QA Director

$156K - $192K - Pittsburgh, PA
In this role, the selected candidate will advise and provide recommendations to C-level decision makers regarding quality standards; initiate activities to improve quality across organization.
industry
e-Commerce
experience
11 - 15 years

Blue Bell, PA
This position is responsible for the management and direction of an individual operation. The role will plan, coordinate and direct order entry, order production for dispensing, verification of prescriptions within corporate and regulatory guidelines. The job function is responsible for managing quality, cost and service targets along with client-specific SLA requirements.
industry
Healthcare IT
experience
11 - 15 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

PA
In this role, you will work with cross functional teams to ensure appropriate integrations between QARA systems and other systems, including ERP systems and training systems.
industry
Medical Devices & Diagnostics
experience
11 - 15 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

Pittsburgh, PA
The Executive is responsible for organizing efforts to support continuous quality improvement of procedures through audits in order to detect, assess, investigate, correct and prevent deficiencies in clinical operations.
industry
Misc. Healthcare
experience
8 - 10 years

$150K - $200K - Bensalem, PA
The Quality Assurance Director Quality Systems is responsible for developing, revising and maintaining quality assurance systems to ensure compliance with cGMPs and contract vendor requirements in a pharmaceutical environment.
industry
Biotech/Pharma
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

Philadelphia, PA
In this role, you will be responsible for planning and implementing the performance improvement program to meet the needs of the hospital.
industry
Misc. Healthcare
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

$120K - $160K - Allentown, PA
The Global Director of Quality will lead a team of Quality professionals across multiple sites who work closely with Operations and Commercial teams to ensure Customer requirements are understood and met.
industry
Manufacturing / Diversified
experience
11 - 15 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

Philadelphia, PA
The Associate Director, Quality Systems will ensure quality and regulatory compliance requirements are identified, documented, integrated, and maintained.
industry
Medical Devices & Diagnostics
experience
8 - 10 years

West Point, PA
In this role, you will ensure that all products produced in the IPT are in conformance to all applicable policies/procedures of Merck, in compliance with cGMPs, and in compliance with all governing regulations.
industry
Biotech/Pharma
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

King Of Prussia, PA
Works with teams to investigate and resolve non-compliance, deviations and process related issues providing recommendations for solutions and CAPAs as needed.
industry
Engineering Services
experience
11 - 15 years

Spring House, PA
In this role, you will organize and lead meetings with key PV business leaders to periodically assess quality metrics and determine if risks are adequately defined and controlled under the IQPs.
industry
Biotech/Pharma
experience
11 - 15 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

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

West Point, PA
In this role, you will manage, process and approve investigations, capa extension requests and change management records.
industry
Biotech/Pharma
experience
11 - 15 years