AstraZeneca Posted July 31, 2026

Specialist - Quality Assurance - 12 Month Secondment/FTC

Macclesfield, United Kingdom Full time
Quality

AstraZeneca is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Specialist Quality (12 Month Secondment/FTC)

Introduction to role:

Join us as a Quality Specialist and provide QA support for aseptic manufacturing, ensuring that operation meet all the regulatory and AstraZeneca standards and the appropriate level of compliance. Your role will directly impact the value stream by supporting and influencing decisions through advice to others.

Accountabilities:

Provide Quality Assurance support to the manufacturing team

Provide technical advice on GMP requirements, quality standards, and the compliance impact of manufacturing and operational activities

Support investigations and ensure appropriate root cause analysis and effective corrective and preventative actions are implemented

Triage, review and close deviations and associated investigations within agreed timelines

Support the complaints management process and, where appropriate, review and approve complaint investigations

Maintain and develop your professional capability

Provide training and coaching to personnel

Perform MSDM documentation updates

Conduct self-inspections and observations

Review batch records

Manage OCM Change control

Proactively suggest improvements to enhance quality compliance

Maintain high quality standards in production and QC testing clean rooms

Participate in regulatory and internal audits and inspections

Essential Skills/Experience:

Qualified to degree level or equivalent in one of the sciences or with working experience in a GMP environment.

Sound knowledge and understanding of the principles of aseptic manufacture and associated GMPs.

Essential Functional Capability at the Professional level in Aseptic Manufacture and Environmental Control.

Knowledge of Current GMP requirements related to technical expertise and regulatory processes.

Desirable Skills/Experience:

Experience with deviation management, change controls, complaints and batch record reviews

Experience driving continuous improvement initiatives within a GMP environment

Understanding of Product Quality Reviews and audit/inspection management

AstraZeneca offers a unique opportunity to be at the forefront of quality assurance, where your work is both important and valued. Our forward-looking mindset allows you to add real value throughout the lifecycle of our products, from discovery to commercialization. As the voice of the patient, every batch you certify is a personal stamp of approval. We are always innovating, trialing the latest models and technologies to improve reliability and excellence in our processes. Here, you'll feel empowered to make decisions that put patients first, working in a collaborative environment that values each voice.

Ready to make a difference? Apply now to join our team!

Date Posted

31-Jul-2026

Closing Date

14-Aug-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.

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Macclesfield, United Kingdom
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 644 comparable Quality roles across 85 biopharma companies.

644Comparable roles tracked
598Currently active
85Companies hiring similar roles
45Countries represented

Salary context

110 of 644 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Technician - QC Laboratory · Lilly $13/hr – $29/hr (≈ $26,998–$60,507/yr)
Highest disclosed · Executive Director, QA Microbiology · Regeneron Pharmaceuticals, Inc (USA) $203,000/yr – $399,400/yr
Peer group range $43,753 – $301,200 (median $159,000)

Where these roles are based

Top locations among the 644 comparable roles

United States213
Ireland49
India45
China39
Singapore36
France29

+ 39 more countries

Seniority mix

309 of 644 peers have a known seniority level

Manager116
Senior97
Associate Director26
Director24
Associate23
Principal14
Senior Director7
Executive/VP1
Intern/Fellow/Postdoc1

Therapeutic area mix

0 of 644 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Regeneron UK Limited Uxbridge1, United Kingdom Associate Director
Same function Same country
40%similar
GlaxoSmithKline Services Unlimited Uk, United Kingdom Senior
Same function Same country
40%similar
GlaxoSmithKline Services Unlimited Uk, United Kingdom Senior
Same function Same country
40%similar
Boehringer Ingelheim Pirbright, United Kingdom
Same function Same country
40%similar
Boehringer Ingelheim Pirbright, United Kingdom
Same function Same country
40%similar
Boehringer Ingelheim Pirbright, United Kingdom
Same function Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Associate Director Inspection Management (GCP)
Regeneron UK Limited · Uxbridge1, United Kingdom · Associate Director
Function Therapeutic area Seniority Country
40%
QA Analyst (Pirbright, United Kingdom, Aberdeen City)
Boehringer Ingelheim · Pirbright, United Kingdom · Seniority not listed
Function Therapeutic area Seniority Country
40%
Associate Quality Lead
Roche · Welwyn, Hertfordshire, United Kingdom · Associate
Function Therapeutic area Seniority Country
40%
Senior Manager QA Auditor GCP Strategy
· Remote, United Kingdom · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.