Quality Assurance Specialist – Global MES & GxP Compliance
Spectraforce
Thousand Oaks, California
Remote
5 days ago
Job Description
Position Title: Quality Assurance Specialist – Global MES & GxP Compliance
Work Location: Remote Worker - Strong presence for EST
Assignment Duration: 12 months (Possible Extension)
Work Arrangement: Remote
Position Summary:
The Quality Assurance Specialist will support global MES projects to ensure compliance, quality assurance, and operational excellence in a GMP-regulated environment.
Background & Context:
Qualification & Experience:
Key Responsibilities:
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 35.00/hr.
Work Location: Remote Worker - Strong presence for EST
Assignment Duration: 12 months (Possible Extension)
Work Arrangement: Remote
Position Summary:
The Quality Assurance Specialist will support global MES projects to ensure compliance, quality assurance, and operational excellence in a GMP-regulated environment.
Background & Context:
- The Quality Assurance team within the Worldwide Operations Manufacturing department is seeking an enthusiastic, results-oriented, and experienced Quality Assurance Specialist to join our organization as a Remote Worker.
- This is an excellent opportunity for a highly experienced and talented individual to contribute to our organization’s mission of serving patients.
Qualification & Experience:
- Bachelor's or Master’s degree in Life Sciences, Engineering, or related field.
- Proven experience in quality assurance within a GMP-regulated manufacturing environment.
- Experience supporting MES and process transformation initiatives.
- Strong understanding of validation principles and regulatory compliance.
- At least 5 years of experience in quality assurance or related roles.
- Hands on with PASX along with associated integrations to Level 2 and Level 4 systems.
- Experience in designing, deploying, and maintaining Körber’s PASX MES system.
- Pharma / GxP regulated environment experience.
- Doctorate degree OR Master degree and 3 years of experience OR Bachelor degree and 5 years of experience OR Associate degree and 10 years of experience OR High school diploma / GED and 12 years of experience.
Key Responsibilities:
- Ensure quality oversight and compliance for MES and PT project activities.
- Support validation and qualification efforts for computerized systems in alignment with GMP requirements.
- Review and approve documentation related to MES workflows, change controls, and deviations.
- Collaborate with cross-functional teams to ensure quality standards are met during system implementation.
- Participate in risk assessments and support mitigation strategies for quality-related issues.
- Ensure that quality processes and procedures are updated and aligned with project deliverables.
- Provide training and guidance on quality practices and regulatory compliance.
- Support audits and inspections by providing documentation and subject matter expertise.
- Monitor and report on quality metrics and continuous improvement initiatives.
- Ensure alignment with global quality standards and local regulatory requirements.
Applicant Notices & Disclaimers
- For information on benefits, equal opportunity employment, and location-specific applicant notices, click here
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 35.00/hr.