Quality Control Analyst (Analytical Molecular Bioassay) in Liverpool

Quality Control Analyst (Analytical Molecular Bioassay) in Liverpool

Liverpool Full-Time 28800 - 43200 £ / year (est.) No working from home possible
AstraZeneca

At a Glance

  • Tasks: Conduct quality control testing and ensure compliance with health and safety guidelines.
  • Company: Join AstraZeneca, a leader in biopharmaceutical innovation.
  • Benefits: Competitive salary, lifelong learning opportunities, and a supportive community atmosphere.
  • Other info: Work a 4 on 4 off shift pattern with excellent career growth potential.
  • Why this job: Make a real impact on life-changing medicines while developing your skills.
  • Qualifications: Degree or HND in a scientific field and experience in GMP/GLP environments.

The predicted salary is between 28800 - 43200 £ per year.

Job Description:

Job information Quality Control Analyst (Analytical Molecular Bioassay) from the Company AstraZeneca, this latest Quality Control Analyst (Analytical Molecular Bioassay) job vacancy is located in the city Liverpool L located in the country United Kingdom . This latest job opening is open to job seekers who have the latest education / graduate GCSE .

Job Responsibility:

Quality Control Analyst (Analytical Molecular Bioassay)

Location: Speke Liverpool

Join us at AstraZeneca\'s Speke location in the UK, where we are committed to unlocking opportunities for lifelong learning and development. We are a team that never stands still, constantly growing our abilities, skills, and knowledge. Our work is inspiring and rewarding, influencing every part of the product lifecycle to deliver life-changing medicines.

At Speke, we research, develop, produce and distribute up to 20 million vaccine doses a year for the global market. Join us and be part of a community atmosphere where everyone feels welcome!

Accountabilities:

As a Quality Control Analyst, you will conduct routine and non-routine investigational and validation testing on products in accordance with the appropriate cGXP procedures, GMP Compliance Rulebook, the Code of Conduct, quality manual and any other company policies. You will provide support to regulatory inspections, lead Quality Control investigations, update GMP documents within the appropriate system, and ensure the compliance of all laboratory procedures and personnel with Health & Safety Guidelines.

Essential skills/experience:

  • Qualified to degree level/HND or equivalent in a scientific field
  • Experience in a Good Manufacturing Practice (GMP) environment / Good Laboratory Practice (GLP)
  • Understanding of Quality Control testing techniques
  • Previous Biopharmaceutical Industry experience

This position will operate a 4 on 4 off, 12 hour days shift pattern.

At AstraZeneca, we take Quality seriously. We are always innovating, trialling the latest models and technologies to improve reliability and excellence in our processes. We are proactive, science-based, and solutions-oriented. Our focus is on scaling and introducing new technologies, using models to predict and proactively manage risk. We work cross-functionally, across sites and regionally, sharing expertise and offering support to others. We are strong communicators and networkers who take personal responsibility for the outcomes.

Join us at AstraZeneca\'s Operations team and pioneer a new\' Quality way. Develop your expertise by being both challenged and supported to apply a modern\' Quality mindset. It means taking accountability and making brave decisions. Whether that\'s reimagining the best way to respond to procedures and regulations, or pushing back when there\'s disagreement.

AstraZeneca is an equal opportunities employer. We welcome applications from all sections of the community. All applicants will be judged on their individual merits and qualifications, regardless of race, gender, age, disability, sexual orientation, religion or belief.

Are you ready to make a difference? Apply now and join us in our mission to deliver life-changing medicines!

Note: Applications will be accepted until 2025-11-02.

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Quality Control Analyst (Analytical Molecular Bioassay) in Liverpool employer: AstraZeneca

AstraZeneca's Speke location in Liverpool is an exceptional employer, dedicated to fostering a culture of continuous learning and development. With a strong commitment to quality and innovation, employees are empowered to grow their skills while contributing to the production of life-changing medicines. The supportive community atmosphere, combined with opportunities for professional advancement and a focus on employee well-being, makes AstraZeneca a truly rewarding place to work.

AstraZeneca

Contact Details:

AstraZeneca Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Quality Control Analyst (Analytical Molecular Bioassay) in Liverpool

Unlock Networking Opportunities

Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like AstraZeneca. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.

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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like AstraZeneca.

Leverage Internships for Full-time Roles

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Tailor Your Approach

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We think you need these skills to ace Quality Control Analyst (Analytical Molecular Bioassay) in Liverpool

Analytical Skills
Good Manufacturing Practice (GMP)
Good Laboratory Practice (GLP)
Quality Control Testing Techniques
Biopharmaceutical Industry Experience
Regulatory Compliance
Investigational Testing

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at AstraZeneca!

Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show AstraZeneca that you're not just a fit for the job but also a safety-conscious candidate!

Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at AstraZeneca!

Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At AstraZeneca, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.

How to prepare for a job interview at AstraZeneca

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at AstraZeneca that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

Showcase Relevant Experience

If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

Know Their Products

Take some time to familiarise yourself with AstraZeneca’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.

Be Ready for Regulatory Scenarios

In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.