Quality Control Project Manager

SSi People; Thousand Oaks (CA); On-site; USD 60,000 - 80,000; Full time

Job summary

SSi People is looking for an MCS Senior Associate Quality Assurance in Thousand Oaks, California. This role requires delivering real-time quality assurance support in a drug substance production facility. Responsibilities include providing compliance support and overseeing manufacturing operations. Candidates should possess a high school diploma or higher with relevant experience, flexibility in shift rotations, and hands-on experience in a GMP environment. The ideal candidate will have strong attention to detail and an ability to adhere to standard operating procedures.

Qualifications

• At least 2 years of work experience or 6 months with an associate's degree.
• Hands-on experience in a GMP environment focusing on quality assurance.
• Demonstrated ability to perform GMP operations and maintain documentation.

Responsibilities

• Provide quality oversight and compliance support on the plant floor.
• Review and approve electronic batch records and SOPs.
• Evaluate compliance issues and ensure timely completion of quality records.
• Represent quality assurance in team projects for operational goals.

Skills

Quality assurance experience

Attention to detail

Flexibility

Education

High school diploma/GED

Associate's degree

Bachelor's degree

Job description

Job Title: MCS Senior Associate Quality Assurance

Location: Thousand Oaks, California (On-site)

Job Summary: We are seeking a dedicated professional to deliver real-time, floor-based quality assurance support within a leading drug substance production facility. Our team values critical thinking, flexibility, and an attention to detail to ensure compliance and operational excellence across manufacturing and facilities operations.

Responsibilities

• Provide daily quality oversight and compliance support across manufacturing and facilities by maintaining a purposeful presence on the plant floor.
• Review and approve electronic batch records, revise and approve standard operating procedures, and handle quality approval of minor deviations.
• Evaluate compliance issues, offer recommendations, and ensure timely progress and completion of quality records.
• Represent the quality assurance function in team-based projects aimed at achieving departmental operational goals within a matrix environment.

Required

• High school diploma/GED with at least 2 years of work experience, OR an associate’s degree with at least 6 months of work experience, OR a bachelor’s degree.
• Proven flexibility to rotate between day and swing shifts every six months, including starting with day shifts for training purposes.
• Hands‑on experience in quality assurance or manufacturing within a GMP environment; strong focus on attention to detail in all aspects of work.
• Demonstrated ability to perform GMP operations, including following SOPs and maintaining good documentation practices.