Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Join our QA team to ensure top-notch quality in pharmaceutical projects.
- Company: Be part of a leading pharmaceutical CDMO with innovative products and a state-of-the-art facility.
- Benefits: Enjoy a dynamic work environment with opportunities for growth and impactful projects.
- Why this job: Make a real difference in pharmaceutical development while collaborating with diverse teams.
- Qualifications: Experience in QA within a GMP environment and strong communication skills are essential.
- Other info: Opportunity to engage in continuous improvement and represent the QA team during audits.
The predicted salary is between 36000 - 60000 £ per year.
Senior QA Officer Nottingham Our client, a leading pharmaceutical CDMO specialising in the development and manufacture of innovative pharmaceutical products, is undergoing significant expansion due to growing international demand. With a state-of-the-art GMP manufacturing facility and a comprehensive drug development portfolio, now is the perfect time to join this dynamic and forward-thinking team. This is an opportunity to be part of a growing company at the forefront of pharmaceutical development. If you’re looking for a challenging and rewarding role with real impact, this could be the perfect fit for you. My client is seeking a skilled and experienced Senior QA Officer to play a pivotal role within the established QA team. This customer-facing position offers the opportunity to work on a range of exciting projects, collaborating closely with cross-functional teams to deliver high-quality pharmaceutical solutions. Key Responsibilities: As the Senior QA Officer, you will: * Act as the QA representative on both new and existing project teams, ensuring quality actions are effectively managed. * Provide expert advice on GMP-related matters and support formulation, manufacturing, and analytical investigations. * Review manufacturing and analytical data, deviations, CAPAs, and change controls to ensure the release of investigational medicinal products meets quality standards. * Lead quality-related investigations, including deviations and CAPAs, while proactively engaging in continuous improvement activities. * Be a key point of contact for client and regulatory audits, representing the QA team and maintaining the Quality System. * Author quality-related documents and ensure compliance with all regulatory requirements. About You: To be successful in this role, you will have: * Demonstrable experience as a QA professional in a GMP-regulated environment with A deep understanding of cGMP regulations and quality management systems. * A proactive approach to identifying and resolving quality issues and a passion for driving continuous improvement. * Strong communication skills and proven experience working within cross-functional teams. * The ability to build strong relationships with both internal teams and external customers. If you’re interested in the above role then please click apply or get in touch to discuss further. Consult will endeavour to contact candidates within 14 days of application. However, if you do not hear back after 2 weeks then please assume on this occasion, unfortunately, you have not been successful
Senior QA Officer employer: Consult, Search and Selection
Contact Detail:
Consult, Search and Selection Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior QA Officer
✨Tip Number 1
Familiarize yourself with the latest cGMP regulations and quality management systems. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high-quality standards in pharmaceutical development.
✨Tip Number 2
Highlight your experience in leading quality-related investigations and your proactive approach to continuous improvement. Be ready to share specific examples of how you've successfully resolved quality issues in past roles.
✨Tip Number 3
Prepare to discuss your communication skills and how you've effectively collaborated with cross-functional teams. Think of instances where your ability to build strong relationships has led to successful project outcomes.
✨Tip Number 4
Research the company’s recent projects and their impact on the pharmaceutical industry. Being knowledgeable about their work will show your genuine interest in the role and help you stand out during discussions.
We think you need these skills to ace Senior QA Officer
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the Senior QA Officer position. Make sure you understand the key responsibilities and required skills, as this will help you tailor your application.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in a GMP-regulated environment. Provide specific examples of how you've successfully managed quality actions and contributed to continuous improvement.
Showcase Communication Skills: Since strong communication skills are essential for this role, include examples in your application that demonstrate your ability to work effectively within cross-functional teams and build relationships with clients.
Tailor Your Documents: Customize your CV and cover letter to reflect the language and requirements mentioned in the job description. Use keywords related to quality management systems and cGMP regulations to make your application stand out.
How to prepare for a job interview at Consult, Search and Selection
✨Showcase Your GMP Knowledge
Make sure to highlight your deep understanding of cGMP regulations during the interview. Be prepared to discuss specific examples from your past experience where you successfully navigated GMP-related challenges.
✨Demonstrate Proactive Problem-Solving
Prepare to share instances where you identified and resolved quality issues proactively. This will showcase your commitment to continuous improvement, which is crucial for the Senior QA Officer role.
✨Emphasize Team Collaboration
Since this position involves working closely with cross-functional teams, be ready to discuss how you've effectively collaborated with different departments in previous roles. Highlight any successful projects that resulted from teamwork.
✨Prepare for Client and Regulatory Audit Scenarios
Anticipate questions related to client and regulatory audits. Think about your experiences representing QA teams during audits and how you maintained compliance with quality systems. This will demonstrate your readiness for the responsibilities of the role.
