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For Companies At a Glance
- Tasks: Lead quality assurance initiatives and support compliance across documentation and processes.
- Company: Join AstraZeneca, a global leader in biopharmaceuticals committed to innovation and patient care.
- Benefits: Enjoy a collaborative work environment with opportunities for remote work and professional development.
- Why this job: Be the voice of the patient while driving innovation and sustainability in quality assurance.
- Qualifications: Degree in a scientific discipline with experience in the pharmaceutical industry and quality systems.
- Other info: This is a 12-month secondment/FTC role with a focus on continuous improvement.
The predicted salary is between 36000 - 60000 £ per year.
Specialist Quality Assurance – 12 Month Secondment/FTC
Speke
Pioneer a ‘new’ Quality way
As the voice of the patient, every batch we certify is a personal stamp of approval. Not something we take lightly, we are always innovating, trialling the latest models and technologies to improve reliability and excellence in our processes.
As QA Specialist you will act as a subject matter expert within QA providing technical and analytical support to the Quality Assurance function within the Speke site in addition to the wider site and global AZ partners. You will be responsible for the management and execution of quality documentation, compliance and quality system business processed within the quality technical department.
We\’ll look to you to bring a focus on innovation, digital uplift, new technologies and sustainability practices across the documentation lifecycle as well as an expert knowledge and understanding of Good Manufacturing Practice.
What you\’ll do:
You will lead by example as a quality professional, supporting continuous improvement and compliance across key documentation and business processes. Your responsibilities include driving LEAN and digital initiatives, utilising process improvement tools, ensuring alignment with AZ standards, and proactively managing quality risks. You will coach others, share best practices, and help uplift capabilities across teams. You’ll also partner with cross-functional teams to meet documentation and compliance requirements, deliver efficient guidance, and actively contribute to regulatory and self-inspections.
Essential Skills & Experience:
- Qualified to degree level / or equivalent in a scientific discipline
- Experience in a Biopharmaceutical/pharmaceutical industry
- Experience in a cGMP environment (Quality assurance, Quality Control or Validation)
- Demonstrated knowledge on quality systems
- Excellent technical writing and communication abilities
- To be able to author standard GxP documentation independently
- An understanding of the overall drug development and commercialization process from development, launch and through life cycle management
- Project Management and Influencing skills
- Demonstrated ability to work cross-functionally and to solve complex problems
- Act as BPO for quality documentation and compliance and provide BPO oversite and management e.g. training, PMR and continuous improvement
So, what’s next…
Are you already imagining yourself in this role? Good, because we can’t wait to hear from you!
Date Posted
26-Jun-2025
Closing Date
06-Jul-2025 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. #J-18808-Ljbffr
Specialist Quality Assurance - 12 Month Secondment/FTC employer: AstraZeneca
Contact Detail:
AstraZeneca Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Specialist Quality Assurance - 12 Month Secondment/FTC
✨Tip Number 1
Familiarise yourself with the latest trends in quality assurance within the biopharmaceutical industry. Understanding current innovations and technologies will not only enhance your knowledge but also demonstrate your commitment to continuous improvement during interviews.
✨Tip Number 2
Network with professionals in the QA field, especially those who have experience in cGMP environments. Engaging with industry experts can provide you with insights and potentially valuable connections that may help you stand out as a candidate.
✨Tip Number 3
Prepare to discuss specific examples of how you've implemented LEAN or digital initiatives in previous roles. Being able to articulate your hands-on experience with process improvement tools will showcase your practical skills and alignment with the job requirements.
✨Tip Number 4
Brush up on your technical writing skills, as this role requires the ability to author GxP documentation independently. Consider creating a portfolio of relevant documents or reports you've authored to demonstrate your capabilities during the interview process.
We think you need these skills to ace Specialist Quality Assurance - 12 Month Secondment/FTC
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in the biopharmaceutical or pharmaceutical industry, particularly in a cGMP environment. Emphasise your technical writing skills and any relevant project management experience.
Craft a Compelling Cover Letter: In your cover letter, express your passion for quality assurance and innovation. Mention specific examples of how you've contributed to continuous improvement and compliance in previous roles, and how you can bring that expertise to the Specialist Quality Assurance position.
Highlight Relevant Skills: Clearly outline your qualifications, especially your degree in a scientific discipline and your knowledge of Good Manufacturing Practice. Include any experience with quality systems and your ability to author GxP documentation independently.
Showcase Cross-Functional Collaboration: Demonstrate your ability to work cross-functionally by providing examples of past collaborations. Highlight how you've partnered with different teams to meet compliance requirements and drive process improvements.
How to prepare for a job interview at AstraZeneca
✨Showcase Your Technical Expertise
As a QA Specialist, it's crucial to demonstrate your knowledge of Good Manufacturing Practice and quality systems. Be prepared to discuss specific examples from your experience in the biopharmaceutical or pharmaceutical industry that highlight your technical skills and understanding of compliance.
✨Emphasise Continuous Improvement
Highlight your experience with LEAN initiatives and process improvement tools. Share instances where you've successfully implemented changes that enhanced quality or efficiency, as this aligns with the role's focus on innovation and sustainability practices.
✨Prepare for Cross-Functional Collaboration
Since the role involves partnering with various teams, be ready to discuss how you've worked cross-functionally in the past. Provide examples of how you’ve influenced others and solved complex problems through collaboration, showcasing your project management skills.
✨Demonstrate Strong Communication Skills
Excellent technical writing and communication abilities are essential for this position. Prepare to discuss how you've authored GxP documentation independently and how you ensure clarity and compliance in your communications with stakeholders.
