Job Market Guide: Director of Quality jobs in Philadelphia

Competition
High
0.873787
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Director of Qualitys in Philadelphia. Director of Qualitys in Philadelphia have between ${} and ${} years of experience, averaging $${} years of experience.

105 Director of Quality jobs in Philadelphia

Titusville, NJ
In this role, you will be responsible for initial quality approval of records in Trackwise as well as monitoring for completion of root cause investigations, CAPA implementation, closure and effectiveness checks.
industry
Biotech/Pharma
experience
5 - 7 years

Rahway, NJ
In this role, you will represent QA as single point of contact and provides QA guidance for studies in a certain TA or in certain countries.
industry
Biotech/Pharma
experience
8 - 10 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

Rahway, NJ
This position will be responsible to perform risk assessments to identify audit targets, conduct audits, develop and maintain audit tools, as well as, review of audit reports.
industry
Biotech/Pharma
experience
11 - 15 years

Kenilworth, NJ
The incumbent develop and execute the strategy for all Quality and GMP compliance related activities relating to the analytical testing and release of biologics and therapeutic protein drug substance across the line of business to ensure compliance with all applicable regulations and specifications.
industry
Biotech/Pharma
experience
11 - 15 years

Kenilworth, NJ
The individual selected will report into the Quality Director Biotech, the Quality Systems Lead is responsible to manage and provide an independent Quality oversight over all GMP related activities across the site and in meeting our Manufacturing Division priorities of: Compliance, Supply, Strategy and Profit Plan.
industry
Biotech/Pharma
experience
11 - 15 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

Somerville, NJ
In this role, you will provide Worldwide Supplier Quality Management leadership in the development, implementation and continuous improvement of the WW Biologics Supplier Quality Management Systems.
industry
Biotech/Pharma
experience
11 - 15 years

West Point, PA
In this role, you will maintain awareness of evolving industry and regulatory trends associated with current Good Manufacturing Practices (cGMP)
industry
Biotech/Pharma
experience
11 - 15 years

LAKE SUCCESS, NY
In this role, the selected candidate will provide direct guidance to manufacturing quality managers and oversees the implementation of new or modifications of current QA and food safety programs to ensure all specifications are followed and incorporated accurately and safely.
industry
Food & Beverage
experience
Not Specified

Horsham, PA
In this role, you will contribute to the overall development, implementation and execution of quality systems in support of the manufacture of pharmaceutical products.
industry
Biotech/Pharma
experience
11 - 15 years

West Point, PA
The individual is responsible for the development and maintenance of Quality Systems at the West Point site in accordance with cGMPs and international regulations, guidelines, procedures, and policies.
industry
Biotech/Pharma
experience
5 - 7 years

Titusville, NJ
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

Whitehouse, NJ
In this role, you will maintain awareness of evolving industry and regulatory trends associated with current Good Manufacturing Practices (cGMP)
industry
Biotech/Pharma
experience
11 - 15 years

Rahway, NJ
The Associate Director, Aggregate Report Quality (ARQ) is responsible for leading and performing activities which support aggregate safety reports, audits/inspections, IT output quality management and aggregate submission activities.
industry
Biotech/Pharma
experience
5 - 7 years

Raritan, NJ
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

Rahway, NJ
The QA Lead will conduct timely and efficient internal communication of resource and data quality matters to Senior Management as appropriate.
industry
Biotech/Pharma
experience
11 - 15 years

West Point, PA
The Associate Director drive quality improvement activities and ensures alignment across the site in the execution of their assigned areas.
industry
Biotech/Pharma
experience
5 - 7 years

Raritan, NJ
In this role, you will contribute to the overall development, implementation and execution of quality systems in support of the manufacture of pharmaceutical products.
industry
Biotech/Pharma
experience
11 - 15 years