At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Quality Assurance Analyst Receiving and Inspectionat our Thousand Oaks, CA site. Here, you will be a vital contributor to our inspiring, bold mission.
Summary:
In this role, you are responsible for performing the day-to-day quality operations for QA
Receiving & Inspection team. Perform inspection and disposition of raw materials to support
manufacturing demand. Revise documents to streamline the process and maintain
compliance.
Title: QA Analyst I
Location: Fully onsite Thousand Oaks, CA
Duration: 6 months
Pay: $30-$40 (Very dependent on level and experience)
Responsibilities:
- Inspect incoming materials to determine if they meet quality requirements for manufacturing.
- Disposition raw material lots by reviewing the documentation to determine if quality requirements have been met.
- Revise documents to support process improvements, corrective actions, division compliance, and audit commitments.
- Administer and maintain relevant databases, preparing and issuing reports related to receiving/inspection metrics.
- Assist in external and internal audits by maintaining audit records, extracting data from databases, and creating reports and collecting relevant data.
- May perform other duties as assigned.
Qualifications:
- Strong interpersonal skills and great attention to detail are necessary.
- Experience working in Inspection and Receiving QA type role
- General Knowledge of FDA regulations, Application of Good Laboratory Practices and Application of Good Manufacturing Practices is preferred.
- Strong team player with effective communication skills and able to handle multiple projects concurrently.
- Experience with Microsoft Excel, Word, and PowerPoint.
- Bachelor's degree in science, engineering or another related technical field strongly preferred.
