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- Tasks: Lead quality improvements and ensure compliance in a dynamic pharmaceutical environment.
- Company: Join a global pharmaceutical business focused on innovation and growth.
- Benefits: Opportunity for professional development in a fast-paced setting.
- Why this job: Be part of a quality-driven culture and make a real impact on site projects.
- Qualifications: Bachelor’s degree in Science or QA discipline with 5 years of relevant experience required.
- Other info: Shortlisting is underway; interviews will be held soon!
The predicted salary is between 43200 - 72000 £ per year.
Qualified Person – North West Biotalent are currently representing an exciting and dynamic global Pharmaceutical business who are seeking to bring on an experienced Qualified Person. This role will be to support with their on-site key projects and, site growth and release work. This role will offer the right individual the opportunity to work in a fast-paced business across a range of dosage forms where they can continue their professional development. Responsibilities: Drive quality improvements across compliance to reduce quality issues, reworks and batch failures. To promote quality culture across the site by liaising with cross functional teams. To define GMP quality standards at all times to those expected and required by the business and our customers. To participate in internal and external audits, and support vendor quality management activities. Requirements: Minimum Bachelor’s degree in Science or QA discipline At least 5 years relevant on the job work experience as a QP on a manufacturing licence. Undertake the duties of a Qualified Person as defined in Directives 2001/83/EC as amended and 2001/20/EC. Shortlisting for this role has begun with a view to holding first stage interviews over the next couple of weeks. For any further information please contact Sarah Pawar at BioTalent on 0203 9115 888, email sarah.pawar@biotalent.com or respond directly to this advert.
Qualified Person employer: BioTalent
Contact Detail:
BioTalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person
✨Tip Number 1
Make sure to highlight your experience with GMP quality standards in your conversations. This is crucial for a Qualified Person role, and demonstrating your knowledge can set you apart.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who have experience as a Qualified Person. They can provide insights and may even refer you to opportunities within their organizations.
✨Tip Number 3
Stay updated on the latest regulations and compliance requirements in the pharmaceutical sector. Being knowledgeable about current trends can help you engage in meaningful discussions during interviews.
✨Tip Number 4
Prepare to discuss specific examples of how you've driven quality improvements in past roles. Concrete examples will demonstrate your capability and commitment to quality culture.
We think you need these skills to ace Qualified Person
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Qualified Person position. Understand the key responsibilities and requirements, especially the importance of quality improvements and compliance.
Tailor Your CV: Customize your CV to highlight your relevant experience as a Qualified Person. Emphasize your background in quality assurance, compliance, and any specific projects that align with the role's responsibilities.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for quality assurance in the pharmaceutical industry. Mention your experience with GMP standards and how you can contribute to the company's quality culture.
Follow Up: After submitting your application, consider following up with a polite email to express your continued interest in the position. This can help keep your application top of mind for the hiring team.
How to prepare for a job interview at BioTalent
✨Understand GMP Standards
Make sure you have a solid grasp of Good Manufacturing Practice (GMP) standards. Be prepared to discuss how you've applied these standards in your previous roles and how you can ensure compliance in this new position.
✨Showcase Your Quality Improvement Initiatives
Think of specific examples where you've driven quality improvements in your past roles. Highlight any initiatives that reduced quality issues or batch failures, as this will demonstrate your proactive approach to quality management.
✨Prepare for Audit Scenarios
Since the role involves participating in internal and external audits, be ready to discuss your experience with audits. Prepare to share how you've handled audit findings and what steps you've taken to improve processes post-audit.
✨Emphasize Cross-Functional Collaboration
This position requires liaising with cross-functional teams. Be prepared to talk about your experience working with different departments and how you fostered a quality culture across those teams.
