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
- 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
- Experience working with eDMS platforms
- Ability to work independently in a remote setting
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