Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Ensure timely reporting of analytical data and manage compliance within the ASG team.
- Company: Join OXB, a pioneer in cell and gene therapy with over 25 years of experience.
- Benefits: Enjoy competitive rewards, wellbeing programmes, and a supportive, inclusive environment.
- Why this job: Make a real impact in healthcare while working with innovative pharmaceutical companies.
- Qualifications: Science graduate with a biological background and knowledge of GMP compliance required.
- Other info: Collaborate with passionate colleagues in state-of-the-art facilities.
The predicted salary is between 36000 - 60000 £ per year.
We pride ourselves on our integrity. We do what’s right for our employees, patients and partners, and so can you. We are currently recruiting for an ASG QC Officer to join the Analytical Services Group (ASG) team. The purpose of this role is to ensure timely reporting of analytical data, provide oversight of ASG compliance, manage stability programs, and continuously improve ASG processes in line with GxP requirements. Our Analytical Services Group supports the development of products through analytical testing to facilitate manufacturing and process development, ensuring appropriate quality controls and use of analytics.
Your responsibilities in this role would be:
- Writing and reviewing SOPs and documentation related to QCO activities
- Assisting with troubleshooting QCO-related issues
- Coordinating stability studies and ensuring timely QC checks of stability reports
- QC checking of submission forms for external testing, reports, and data in COA/COT
- Coordinating and arranging outgoing shipments to external testing facilities
- Tracking and monitoring departmental quality records and reporting metrics
- Training team members in multiple processes/procedures
- Managing and overseeing QCO processes
- Providing analytical and stability updates to internal and external customers
- Inputting into the validation of analytical spreadsheets
- Generating and issuing stability plans, protocols, and reports at each time point
- Performing trend analysis of assay controls and standards
- Creating, managing, and QC checking stability trackers
- Generating batch-specific COA and COT and maintaining the QC database
- Updating product specifications and reporting data to customers
- Performing calculation checks for QC release assays
- Generating monthly metrics for the Head of Department
- Managing departmental quality records and liaising with external testing labs
We are looking for:
- Science graduate with a biological background or experience working within a pharmaceutical regulated environment
- Knowledge of QC testing within a GMP environment
- Computer literacy (Word, Excel, MS Office)
- Detailed understanding and ability to uphold/improve GMP compliance for ASG processes and procedures
- Ability to communicate effectively both internally and externally
- Strong problem-solving skills and ability to make informed decisions
- Excellent time management and organizational skills
- Ability to work independently and as part of a team
- Highly motivated with excellent attention to detail
About Us: OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 25 years of experience in viral vectors; the driving force behind the majority of gene therapies. OXB collaborates with some of the world’s most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV), and adenoviral vectors. OXB’s world-class capabilities span from early-stage development to commercialization. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.
What’s in it for you:
- Highly competitive total reward packages
- Wellbeing programmes
- Development opportunities
- Welcoming, friendly, supportive colleagues
- A diverse and inclusive working environment
Our values are: Responsible, Responsive, Resilient, Respect. State-of-the-art laboratory and manufacturing facilities. We want you to feel inspired every day. We’re future-focused and our business is growing rapidly. We succeed together through passion, commitment and teamwork, and so can you. Collaborate. Contribute. Change lives.
ASG QC Officer employer: OXB
Contact Detail:
OXB Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land ASG QC Officer
✨Tip Number 1
Familiarise yourself with GxP regulations and GMP compliance, as these are crucial for the ASG QC Officer role. Understanding these guidelines will not only help you in interviews but also demonstrate your commitment to quality assurance.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those involved in quality control and analytical services. Engaging with them can provide insights into the role and may even lead to referrals or recommendations.
✨Tip Number 3
Brush up on your problem-solving skills by tackling case studies or scenarios related to QC issues. Being able to discuss how you would approach real-world challenges during your interview can set you apart from other candidates.
✨Tip Number 4
Prepare to discuss your experience with analytical software and tools, particularly Excel, as this is a key requirement for the role. Highlight any specific projects where you've used these skills to improve processes or outcomes.
We think you need these skills to ace ASG QC Officer
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the ASG QC Officer position. Highlight the key responsibilities and required skills, such as writing SOPs, managing stability programs, and ensuring compliance with GxP requirements.
Tailor Your CV: Customise your CV to reflect your relevant experience in quality control and analytical testing. Emphasise your educational background in science, any experience in a GMP environment, and your proficiency with software like Word and Excel.
Craft a Compelling Cover Letter: Write a cover letter that showcases your problem-solving skills and ability to communicate effectively. Mention specific examples from your past experiences that demonstrate your attention to detail and organisational skills, aligning them with the responsibilities of the role.
Highlight Soft Skills: In your application, don't forget to mention your soft skills, such as teamwork, time management, and motivation. These are crucial for the ASG QC Officer role, where collaboration and independent work are both important.
How to prepare for a job interview at OXB
✨Showcase Your Scientific Knowledge
As an ASG QC Officer, a strong understanding of biological sciences is crucial. Be prepared to discuss your educational background and any relevant experience in a pharmaceutical regulated environment. Highlight specific examples where you've applied your scientific knowledge in quality control settings.
✨Demonstrate Attention to Detail
This role requires excellent attention to detail, especially when it comes to writing and reviewing SOPs and documentation. During the interview, provide examples of how you've ensured accuracy in your previous work, particularly in QC processes or data management.
✨Emphasise Problem-Solving Skills
The ability to troubleshoot QCO-related issues is key for this position. Prepare to discuss past challenges you've faced in quality control and how you approached solving them. This will show your potential employer that you can think critically and act decisively.
✨Communicate Effectively
Effective communication is essential for coordinating with team members and external partners. Practice articulating your thoughts clearly and concisely. You might also want to prepare questions to ask the interviewer about their communication practices within the team.
