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Quality Systems Specialist III Remote Part Time
Job Location:
Job Location:
Santa Monica, CA - USA
Salary:
Not provided by the employer
Salary:
Posted:
17 September 2026 (21 hours ago)
Posted:
Application Deadline:
15 December 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
This is a remote position.
Our client a world leader in biotechnology and life sciences is looking for a Quality Systems Specialist III.
Location: Remote PST Hours
Preferred Location: California Foster City or Santa Monica
Schedule: Part-Time approximately 1015 hours per week; may increase to 2025 hours during peak periods
Job Duration: Long term
Rate: $65-$68/hr on W2
Company Benefits: Medical Paid Sick Leave 401 (k)
We are seeking an experienced Quality Systems & Management Review Specialist to support Quality Management System (QMS) activities and quarterly Executive Management Reviews within a global life sciences organization. This role will focus on compiling and analyzing quality data coordinating inputs from global stakeholders and developing executive-level presentations and deliverables.
The ideal candidate will have strong experience with Quality Systems Management Review Veeva QMS and PowerPoint along with the ability to effectively manage deliverables across cross-functional and global Quality teams.
Key Responsibilities
- Compile and organize quality data and metrics to support Quarterly Executive Management Reviews.
- Develop professional PowerPoint presentations using input and data from global business and Quality stakeholders.
- Coordinate and manage inputs timelines and deliverables from cross-functional contributors.
- Collaborate with global Quality teams to ensure timely and accurate completion of Management Review deliverables.
- Review Quality System reports dashboards and metrics in Veeva QMS to support executive-level reporting and presentations.
- Analyze and summarize quality trends and data for management review discussions.
- Provide general support for QMS processes including:
- Deviation Management
- CAPA
- Document Control
- Change Control
- Deviation Management
- Track action items and follow up with stakeholders as needed.
- Support continuous improvement and other Quality Systems activities as assigned.
Required Qualifications
- Bachelors degree in Life Sciences Quality Engineering or a related field.
- 5 years of experience in Quality Systems and/or Quality Management within the pharmaceutical biotechnology medical device or life sciences industry.
- Demonstrated experience supporting Quality Management Reviews / Management Review processes.
- Hands-on experience with Veeva QMS is required.
- Strong Microsoft PowerPoint skills with experience developing executive-level presentations.
- Experience working with Quality metrics dashboards and management reporting.
- Strong organizational skills with the ability to manage multiple deliverables and deadlines.
- Ability to coordinate effectively with global and cross-functional stakeholders.
- Excellent written and verbal communication skills.
Preferred Qualifications
- Experience with Document Control Deviations CAPA and Change Control.
- Experience working in a GxP/GMP-regulated environment.
- Experience presenting or preparing materials for senior/executive Quality leadership.
- Experience with Veeva Quality dashboards and reporting.
- Experience supporting global Quality organizations.
If interested please share your updated resume at /
Required Skills:
Veeva QMS
