What are the responsibilities and job description for the MCS Senior Associate Quality Assurance position at SSi People?
Job Title: MCS Senior Associate Quality Assurance
Location: Thousand Oaks, California (On-Site)
Job Summary: We are supporting a high-impact quality assurance opportunity for a detail-oriented professional who can provide real-time, floor-based oversight in a GMP manufacturing environment. Our team is seeking someone who can partner closely with Manufacturing and Facilities & Engineering teams to help maintain compliance, support documentation review, and contribute to the execution of quality systems.
Responsibilities
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from SSi People and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: SSi People Privacy Policy
Location: Thousand Oaks, California (On-Site)
Job Summary: We are supporting a high-impact quality assurance opportunity for a detail-oriented professional who can provide real-time, floor-based oversight in a GMP manufacturing environment. Our team is seeking someone who can partner closely with Manufacturing and Facilities & Engineering teams to help maintain compliance, support documentation review, and contribute to the execution of quality systems.
Responsibilities
- Provide purposeful presence on the floor and deliver real-time quality assurance support in manufacturing and facility areas.
- Review electronic batch records, evaluate compliance issues, and help ensure quality records progress to completion.
- Support SOP revision and approval, work order approval, and quality approval of minor deviations.
- Serve as a quality liaison for projects and daily operations within a matrixed team environment.
- Ability to work fully onsite in Thousand Oaks, California.
- Willingness and flexibility to rotate shifts every 6 months, including day, swing, and graveyard schedules as needed.
- Experience in a GMP environment with hands-on quality assurance or manufacturing experience, preferably in biotech.
- Strong attention to detail, critical thinking skills, and the ability to make quality-based decisions to ensure compliance.
- Demonstrated ability to follow detailed SOPs, maintain training, and apply good documentation practices.
- High school/GED plus 2 years of work experience, or associate’s degree plus 6 months of work experience, or bachelor’s degree.
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from SSi People and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: SSi People Privacy Policy