Senior Specialist - Quality Assurance (Night shift)

Are you ready to make a significant impact in the world of aseptic manufacturing and packing? The Senior Specialist - Quality Assurance is accountable for delivering QA leadership and oversight for aseptic manufacturing and packaging operations on the night shift. You will provide GMP and aseptic processing expertise, assure cleanroom compliance, influence operational decisions within the Process Execution Team (PET), and support timely and compliant product release. This role is pivotal in safeguarding patient safety, regulatory compliance, and value stream performance.

•

Provide technical guidance on cleanroom standards, aseptic techniques, and environmental controls aligned to current

and internal procedures. •

Advise on deviations, lead or contribute to root cause analysis, and agree

to prevent recurrence and improve process robustness. •

Support or perform product release activities as required, ensuring batch documentation, data integrity, and compliance. •

Complete required PET GMP training and coach manufacturing personnel on

, aseptic behaviours, data integrity, and contamination control. •

Proactively identify compliance risks and opportunities for business improvement, efficiency savings, and

optimization. •

Lead or support local/cross-functional change controls ensuring validated state and regulatory alignment. •

Contribute to

, quality risk management, metrics (e.g., deviations, CAPA effectiveness), and documentation updates.

function, along with a strong understanding of

and how they work together to achieve

in a

environment. •

with strong understanding of cross-functional operations in a lean environment. •

knowledge, including cleanroom behaviours and contamination control principles. •

and working familiarity with

,

, and data integrity principles. •

skills with cultural awareness; ability to coach operators and technicians. •

within general operating guidelines using risk-based, science-led judgment. •

availability.

•

•

, including environmental monitoring, sterility assurance concepts, and interpretation of microbiological data. •

application (FMEA, HACCP). At AstraZeneca, we are committed to quality that goes beyond compliance - driven by a proactive, science-based approach that prioritizes patient safety and product excellence. We foster an inclusive community where collaboration is key, allowing us to innovate and adapt swiftly. With a focus on growth and innovation, you'll find endless opportunities to develop your expertise and contribute to groundbreaking advancements in healthcare! Ready to take on this exciting challenge? Apply now and be part of a team that makes a real difference! We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, colour, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

30-Oct-2026

14-Nov-2026 Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.