We are seeking an experienced Quality Management System (QMS) Manager to support a reputable pharmaceutical organization. This role will focus on maintaining and improving QMS processes ensuring compliance with US and EU regulatory requirements and supporting key quality operations in a remote environment.
Key Responsibilities
Manage and support core QMS processes including CAPA Deviations Change Controls and Vendor Management
Ensure compliance with US FDA and EU pharmaceutical regulations
Provide support for electronic Document Management Systems (eDMS) and quality documentation
Drive continuous improvement initiatives within the QMS framework
Collaborate with cross-functional teams to ensure quality and compliance standards are met
Support audit readiness and regulatory inspections
Required Qualifications
Minimum 7 years of experience in pharmaceutical Quality Management Systems
Strong knowledge of US and EU QMS requirements
Hands-on experience with CAPA Deviations Change Control and Vendor Management
Experience working with eDMS platforms
Ability to work independently in a remote setting
Job Title: QMS Manager Pharmaceutical Location: Remote (East Coast Preferred) Type: Contract (40 hrs/week Industry: Pharmaceutical Job Summary: We are seeking an experienced Quality Management System (QMS) Manager to support a reputable pharmaceutical organization. This role will focus on mai...
Job Title: QMS Manager Pharmaceutical
Location: Remote (East Coast Preferred)
Type: Contract (40 hrs/week
Industry: Pharmaceutical
Job Summary:
We are seeking an experienced Quality Management System (QMS) Manager to support a reputable pharmaceutical organization. This role will focus on maintaining and improving QMS processes ensuring compliance with US and EU regulatory requirements and supporting key quality operations in a remote environment.
Key Responsibilities
Manage and support core QMS processes including CAPA Deviations Change Controls and Vendor Management
Ensure compliance with US FDA and EU pharmaceutical regulations
Provide support for electronic Document Management Systems (eDMS) and quality documentation
Drive continuous improvement initiatives within the QMS framework
Collaborate with cross-functional teams to ensure quality and compliance standards are met
Support audit readiness and regulatory inspections
Required Qualifications
Minimum 7 years of experience in pharmaceutical Quality Management Systems
Strong knowledge of US and EU QMS requirements
Hands-on experience with CAPA Deviations Change Control and Vendor Management