Top Quality Manager Jobs

The Manager/Sr. Manager, Quality Control will lead the QC function, implementing the company's quality control strategy, collaborating with development and operations teams, and managing external resources. The role requires strong interpersonal skills to ensure adherence to quality standards and oversight of analytical processes related to GMP stages.

The QA/QC Manager is responsible for developing and maintaining quality programs to ensure compliance with standards. They oversee quality audits, manage resources, conduct QA/QC inspections, investigate customer complaints, and ensure products meet regulatory standards. The role includes leadership responsibilities and the provision of training to staff.

The Site Manager oversees the construction quality of SPARC plant systems, ensuring compliance with quality standards and regulations. Responsibilities include developing quality strategies, fostering collaboration with engineering teams, conducting site audits, managing QA documentation, addressing quality issues, and leading contract QA/QC field technicians.

The Senior Manager/Associate Director, QA Operations will provide oversight and support for GMP manufacturing activities, reviewing and approving batch records, testing protocols, and related documentation. This role involves leading quality investigations, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to promote a safe and efficient work environment.

The Manager, Quality Control Analytical oversees the QC Analytical laboratory, ensures compliance and timely execution of testing, manages a team of QC Analysts, and collaborates with other teams to address quality control issues. Responsibilities include approving deviations and driving continuous improvement initiatives.

The QA/QC Document Control Manager oversees project document control systems, ensuring compliance with specifications. Responsibilities include managing the filing structure, coordinating document flow between teams, updating documentation, and supporting quality assurance tasks. The role requires strong organizational skills and the ability to improve processes as well as maintaining the integrity of project documentation.

The QC Senior Manager will lead contamination control efforts, ensuring compliance with FDA and EU standards, developing risk assessments, maintaining environmental integrity, and interfacing with various teams to enhance product quality. Responsibilities include supporting microbiology audits, implementing training programs, and contributing to validation and trending analysis.

The Quality Operations Manager/Sr. Manager oversees quality assurance for manufacturing activities at Corcept and Contract Manufacturing Organizations. Responsibilities include ensuring compliance with cGMP, managing quality assessments, performing product disposition, and supporting internal and external audit processes. The role requires strong collaboration with cross-functional teams to mitigate compliance risks and drive quality improvements in drug manufacturing.

The Senior Manager, Quality will lead the Manufacturing Quality team to ensure compliance with regulatory standards and maintain high quality in production. Responsibilities include managing quality systems, investigating quality issues, conducting audits, collaborating with cross-functional teams, and preparing quality reports.

The Quality Control Manager will oversee quality control throughout the production process, develop processes and systems to ensure compliance with standards, conduct inspections, and collaborate with teams and suppliers to address quality issues and drive improvements.

The Quality Systems Manager ensures compliance with quality management standards in industries such as medical and aerospace. Responsibilities include managing QMS processes, leading audits, and driving continuous improvement initiatives.

The Quality Supervisor will oversee and coordinate quality assurance activities, provide technical training to QA staff, ensure compliance with HACCP and GMPs, conduct audits, and collaborate with operations to address quality and safety issues. This role involves inspecting products and managing customer complaints.

The Head of Quality is responsible for ensuring compliance with FDA and international regulations for medical devices, leading the Quality Assurance team, managing the Quality Management System (QMS), and overseeing quality systems documentation and training. This role involves interaction with regulatory agencies, leading audits, and integrating quality assurance practices across departments to enhance patient safety and market access.

The Quality Director will lead quality assurance efforts, ensuring compliance with ISO standards and FDA regulations while mentoring the US Quality Team and collaborating closely with engineering on product development and quality assurance processes. Responsibilities include conducting audits, analyzing quality data, and reporting on QMS performance.

As a Provider Quality Improvement Manager, you will coach healthcare providers to improve care systems and delivery. This role involves maintaining relationships with healthcare entities, leading quality measurement activities, and developing outreach strategies to enhance provider communications and performance in HEDIS measures.

The Supervisor of Quality Control will coordinate quality control activities, supervise QC staff, ensure compliance with regulations, oversee product inspections, manage non-conformance issues, lead training efforts, and continuously improve quality metrics.

The Director of Quality and Mission Assurance is responsible for establishing quality processes, leading AS9100 certification efforts, ensuring product quality standards are met, and developing quality metrics. The role includes managing quality assurance staff, conducting audits, and collaborating on product development, while achieving budgetary objectives and ensuring compliance with government requirements.