We are seeking an experienced Qualified Person (QP) to join a high-performing team within the pharmaceutical industry. This is a confidential opportunity for a driven professional who is passionate about ensuring quality and compliance in a sterile manufacturing environment.
Key Responsibilities:
* Serve as a Qualified Person with oversight of batch certification for sterile products.
* Lead operational quality initiatives to support inspection readiness and maintain compliance with regulatory requirements.
* Provide expert advice on quality standards, ensuring the safety, efficacy, and compliance of products.
* Play a pivotal role in preparing and hosting internal and external audits.
Requirements:
* Qualified Person (QP) status with substantial experience in sterile manufacturing.
* Proven expertise in operational quality and inspection readiness within the pharmaceutical industry.
* Strong leadership and stakeholder management skills, with a focus on collaborative problem-solving.
* Ability to work on-site five days a week to provide hands-on support.
Why Join?
This role offers an excellent compensation package, reflecting the importance of attracting the best talent in the industry. You’ll have the opportunity to make a meaningful impact, working on cutting-edge pharmaceutical products while advancing your career in a supportive environment.
Contact us in confidence to discuss this exclusive opportunity further.
You must be a UK resident to apply.