Astrazeneca Internship Jobs (NOW HIRING)

Position Summary:

AstraZeneca isseekingan energetic and experienced individual with cell therapy quality assurance background to join our Quality Assurance (QA) team. The successful candidate will contribute to the advancement of our product pipeline by performing QA batch record review, label review and verifications, document archival of records, and other assigned tasks. You will also be expected to independently organize and manage timelines for batch record reviews. You will be expected to provide support for both the Santa Monica, CA and Tarzana, CA sites as needed.

Responsibilities include, but are not limited to:

• Reviews routine manufacturing batch documentation and quality control data for in-process and finished product to support disposition and lot closure.

• Review routine material release documentation for quality release of raw materials used for manufacturing and quality control testing.

• Work with Doc Control to ensure archival of batch records.

• Work with QA doc control to ensureaccurateissuance of batch record documentation (i.e.lot/media records and labels) tomanufacturing.

• Provide quality assurance support across technical operations functions (i.e.Manufacturing, Facilities & Engineering, Supply Chain, Quality Control, Analytical Development, Product Development/Manufacturing Sciences & Technology) within AZ toassurecompliance with the quality manual andmaintaincollaborative quality relationships.

• Perform other duties as requested by supervisor/manager to support Quality.

• Administrative Tracking of QA metrics

• On the Floor QA support

Qualifications:

• BA/BS in Biology, Chemistry, Microbiology, Engineering, or a related field is required (no prior work experience needed). Alternatively, an Associate's degree with up to 2 years of relevant experience or a High School diploma with up to 4 years of relevant experience is required. Relevant academic laboratory experience, coursework, or internships are a plus.

• Must be able to work on multiple projects simultaneously anddemonstrateorganizational, prioritization, and time managementproficiencies.

• Flexibility of occasionally workinginweekendor holidays to support lot release.

• Demonstrated ability to take ownership, initiative, and self-accountability.

• Demonstrated ability to collaborate, work, and communicate effectively across organizational interfaces in a fast-paced dynamic team setting.

• Attention to detail and quick learning/application of concepts and information.

• Knowledge of cell culture techniques andproficientin MS Word, Excel, PowerPointand other applications.

• Ability to communicate and work in a self-guided manner with scientific/technical personnel.

Preferred Qualifications:

• Experience in Cell or Gene Therapy

• Well versed in various cell therapy manufacturing processes