Job Title
We are seeking a seasoned Quality Assurance Director to lead our client's strategic QA project in Valencia, Spain.
This 6-month contract role requires a strong QA expert with leadership experience in GMP environments. You will be working directly with one of our clients focused on chemical processes involving polymers, APIs, excipients, and pharmaceutical substances.
- Lead the QA team in a CDMO environment.
- Oversee regulatory compliance and quality control activities.
- Support the client in preparing a PPQ for FDA submission.
- Ensure compliance with current GMP regulations.
Key Qualifications
Strong QA experience in the pharmaceutical industry.Background working with clients in clinical and development phases.Solid understanding of regulatory processes, especially with the FDA.Proven leadership skills to manage multidisciplinary teams in dynamic settings.Fluency in both Spanish and English.Requirements
Available onsite in Valencia (relocation support available for the right candidate).Apply now and make a real impact on regulatory submissions for the U.S. FDA.