At a Glance
- Tasks: Join our QC team to test and report on vital materials for product release.
- Company: Oxford Biomedica is a leader in viral vector development, transforming lives through innovative therapies.
- Benefits: Enjoy competitive rewards, wellbeing programs, and a supportive, inclusive work environment.
- Why this job: Be part of a passionate team making a real impact in cell and gene therapy.
- Qualifications: HND/Degree in Microbiology or related field; experience in microbiology lab techniques required.
- Other info: Flexible shift work from 07:00 to 15:00, Monday to Friday.
The predicted salary is between 30000 - 42000 £ per year.
Job description:
We want you to feel inspired every day. We’re future-focused and our business is growing. We succeed together through passion, commitment, and teamwork, and so can you.
We are currently recruiting for a QC Microbiologist to join the Quality Control team. The purpose of this role is to test and report on raw materials, intermediates, finished products, the manufacturing environment and stability samples to enable product release and meet regulatory requirements.
Your responsibilities in this role would be:
- Test and report on raw materials, intermediates, finished products and the manufacturing environment to enable product release to meet regulatory requirements.
- Participate in continuous improvement initiatives to enhance working practices.
- Support internal audits to maintain and improve Quality systems.
- Maintain stock control of QC test materials for use within the Microbiology Lab and Production areas.
- Co-ordinate microbiology OOS/OOT results to help identify contributory factors and assign root cause.
- Review and update departmental documentation.
- Support Senior Microbiologist and QC Manager with training of new staff.
- Report to Team Lead.
We are looking for:
- HND/Degree level qualified in Microbiology or related subject
- Thorough understanding of microbiological test methods and their application in OXB.
- Understanding of microbiological identification techniques and their use.
- Relevant experience in Microbiology laboratory techniques
- Basic knowledge of cGMP
- Computer literate (Word, Excel), Good familiarity with Microsoft Office software
- Flexibility to work shifts covering the hours from 07.00 to 03.00 Mon-Fri
About Us:
Oxford Biomedica 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.
Oxford Biomedica 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. Oxford Biomedica’s world-class capabilities span from early-stage development to commercialisation. 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: Deliver Innovation, Be Inspiring and Have Integrity
- 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
We offer:
Oxford Biomedica is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, Oxford Biomedica has more than 25 years of experience in viral vectors, the driving force behind the majority of gene therapies.
Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patient’s cells. One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients’ cells. This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy).
Oxford Biomedica 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. Oxford Biomedica’s world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise.
QC Microbiologist employer: OXB
Contact Detail:
OXB Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Microbiologist
✨Tip Number 1
Familiarize yourself with the specific microbiological test methods mentioned in the job description. Understanding these techniques will not only help you during the interview but also demonstrate your commitment to the role.
✨Tip Number 2
Research Oxford Biomedica's recent projects and collaborations in cell and gene therapy. Being knowledgeable about their work will allow you to engage in meaningful conversations during the interview and show your genuine interest in the company.
✨Tip Number 3
Prepare to discuss your experience with cGMP and how it relates to quality control in microbiology. Highlighting your understanding of regulatory requirements will set you apart as a candidate who is ready to contribute from day one.
✨Tip Number 4
Be ready to share examples of how you've participated in continuous improvement initiatives in previous roles. This aligns with the company's values and shows that you are proactive about enhancing working practices.
We think you need these skills to ace QC Microbiologist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your qualifications in Microbiology, relevant laboratory techniques, and any experience with cGMP. Use keywords from the job description to align your skills with what Oxford Biomedica is looking for.
Craft a Strong Cover Letter: In your cover letter, express your passion for microbiology and how your background aligns with the responsibilities of the QC Microbiologist role. Mention specific experiences that demonstrate your ability to contribute to continuous improvement initiatives.
Showcase Teamwork Skills: Since teamwork is emphasized in the job description, provide examples of how you've successfully collaborated with others in previous roles. Highlight any experience in training new staff or participating in audits.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial in a quality control role.
How to prepare for a job interview at OXB
✨Show Your Microbiological Expertise
Be prepared to discuss your understanding of microbiological test methods and identification techniques. Highlight any relevant experience you have in laboratory techniques, as this will demonstrate your capability to perform the tasks required for the QC Microbiologist role.
✨Emphasize Teamwork and Collaboration
Since the company values teamwork, share examples of how you've successfully collaborated with colleagues in previous roles. Discuss any experiences where you contributed to continuous improvement initiatives or supported training for new staff.
✨Familiarize Yourself with cGMP Standards
Understanding current Good Manufacturing Practices (cGMP) is crucial for this position. Brush up on these standards and be ready to explain how you have applied them in your past work, especially in relation to quality control and regulatory compliance.
✨Prepare for Shift Flexibility Questions
The role requires flexibility to work shifts from 07:00 to 03:00, Monday to Friday. Be honest about your availability and willingness to adapt to shift work, and consider discussing any previous experiences you have had with flexible working hours.