At a Glance
- Tasks: Oversee quality and compliance in clinical development, planning global audits.
- Company: Haleon, a leader in the pharmaceutical industry focused on quality.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborate with stakeholders to promote a culture of compliance and quality.
- Why this job: Make a real impact on clinical quality and compliance in a dynamic environment.
- Qualifications: Strong background in pharmaceuticals and extensive QA/auditing experience.
The predicted salary is between 80000 - 100000 £ per year.
Haleon is looking for a qualified professional to oversee quality and compliance during clinical development processes. This role primarily involves planning global audits and ensuring adherence to GCP and GLP regulations.
Candidates should have a strong background in the pharmaceutical industry, alongside extensive experience in clinical quality assurance and auditing. The successful applicant will promote compliance and quality culture while liaising with various stakeholders, supporting key business initiatives.
Senior Clinical QA & Compliance Director (GCP/GLP) in Surrey employer: Haleon
Haleon is an exceptional employer that prioritises a culture of quality and compliance, making it an ideal workplace for professionals in the pharmaceutical industry. With a strong commitment to employee development, we offer numerous growth opportunities and a collaborative environment where your expertise in clinical quality assurance can thrive. Located in a vibrant area, our team enjoys a supportive atmosphere that values innovation and integrity, ensuring that every employee feels valued and empowered to make a meaningful impact.
