The Role
The Director Quality Assurance will be overall accountable for the quality of all products and materials that are released at sites. The role holder provides leadership to an organization of approximately 50 staff located on site. The Director Quality Assurance reports directly into the VP Quality Assurance, with a dotted reporting line to the Plant Manager.
The responsibilities can be divided into three main areas:
> Execution, maintenance, adherence and improvement of the Site Quality Management System
> Assurance that all product released are manufactured in compliance with the Quality Management System, registration dossiers and GMP requirements
> All aspects of financials and personnel within the Quality Assurance function
The Requirements
- Have at least 5 years' experience from managing a professional Quality Assurance function in the pharmaceutical industry
- Have proven knowledge on requirements and applications of pharmaceutical quality systems, GMP, ISO and other relevant standards
- Have strong organizational skills as well as an ability to prioritize and make decisions
- Have leadership experience with control of team budget
- Be fluent in Norwegian (or another Scandinavian language) and English
Additional Benefits
- Competitive base salary, reflective of the local market
- End of year Key Performance Index bonus
- Competitive health insurance and company pension
- Vacation allowance
- Relocation support
- On-boarding support