Contract Onsite QA Associate, Drug Substance (GMP)

Aditi Consulting; Thousand Oaks (CA); On-site; USD 41,328 - 44,083; Part time

Benefits offered by this job

Medical, dental, and vision benefits

Paid time off

Retirement plan participation with employer match

Job summary

A leading consulting firm in California is seeking a Senior Associate, Quality Assurance to oversee Drug Substance manufacturing areas and ensure compliance within a GMP environment. The role involves real-time QA support, along with responsibilities like batch record review and SOP approvals. Ideal candidates will have a Bachelor’s Degree in a relevant field, hands-on QA or manufacturing experience, and strong critical thinking skills. Full-time employees receive comprehensive benefits including health insurance and retirement plans.

Qualifications

• Demonstrated ability to perform GMP operations, including following detailed SOPs.
• Experience managing projects through completion and meeting timelines.
• Effective written and verbal communication skills.

Responsibilities

• Provide daily oversight of the Drug Substance manufacturing areas.
• Support and enforce compliance oversight to Manufacturing and Facilities & Engineering.
• Evaluate compliance issues and ensure progress of quality records.

Skills

Critical thinking ability

Organizational skills

Team-player mindset

Education

Bachelor's Degree in Biochemistry, Biology, Chemistry, or related science field

Job description

A leading consulting firm in California is seeking a Senior Associate, Quality Assurance to oversee Drug Substance manufacturing areas and ensure compliance within a GMP environment. The role involves real-time QA support, along with responsibilities like batch record review and SOP approvals. Ideal candidates will have a Bachelor’s Degree in a relevant field, hands-on QA or manufacturing experience, and strong critical thinking skills. Full-time employees receive comprehensive benefits including health insurance and retirement plans.