Senior Specialist - Quality Assurance (Night shift)

Macclesfield, United Kingdom
Today
Job Type
Permanent
Work Pattern
Full-time
Work Location
On-site
Seniority
Senior
Education
Degree
Visa Sponsorship
Available
Posted
29 Jul 2026 (Today)

Benefits

Pension Private healthcare Life assurance Income protection Annual bonus Share schemes Flexible working options Employee assistance programme Wellbeing initiatives

Job Title: Senior Specialist – Quality Assurance

Night Shift (4 on, 4 off)

Location: Macclesfield

Competitive salary and benefits

Introduction to role:

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.

Accountabilities:

  • Cleanroom and Aseptic Oversight: Provide technical guidance on cleanroom standards, aseptic techniques, and environmental controls aligned to currentEU GMP Annex 1 and internal procedures.
  • Deviation and CAPA Management: Advise on deviations, lead or contribute to root cause analysis, and agreeCAPAs to prevent recurrence and improve process robustness.
  • Product Quality/Release Support: Support or perform product release activities as required, ensuring batch documentation, data integrity, and compliance.
  • GMP Training and Coaching: Complete required PET GMP training and coach manufacturing personnel oncGMP, aseptic behaviours, data integrity, and contamination control.
  • Compliance and Continuous Improvement: Proactively identify compliance risks and opportunities for business improvement, efficiency savings, andlean optimization.
  • Change Control: Lead or support local/cross-functional change controls ensuring validated state and regulatory alignment.
  • Quality Systems Execution: Contribute toPQR, quality risk management, metrics (e.g., deviations, CAPA effectiveness), and documentation updates.

Essential Skills/Experience:

  • Degree (or equivalent) in a scientific discipline (e.g., pharmacy, microbiology, chemistry, biochemistry, engineering). A clear, comprehensive grasp of thequality assurance function, along with a strong understanding ofother business functions and how they work together to achievebusiness objectives in alean manufacturing environment.
  • Quality Assurance in Pharmaceutical Manufacture with strong understanding of cross-functional operations in a lean environment.
  • Aseptic Processing or Packing knowledge, including cleanroom behaviours and contamination control principles.
  • Current GMP Knowledge and working familiarity withEU GMP Annex 1,ICH Q9/Q10, and data integrity principles.
  • Communication and Influencing skills with cultural awareness; ability to coach operators and technicians.
  • Decision-Making within general operating guidelines using risk-based, science-led judgment.
  • Permanent Night Shift availability.

Desirable Skills/Experience:

  • Experience in Aseptic Manufacturing operations and sterile packaging lines.
  • Microbiology Experience, including environmental monitoring, sterility assurance concepts, and interpretation of microbiological data.
  • Quality Risk Management 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.

Date Posted

29-Jul-2026

Closing Date

12-Aug-2026Our 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.

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