Freelance Interim QA Director

Company Description

ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in Australia, Canada, Germany, Japan, the Netherlands, Sweden, United Kingdom, and the United States, ProPharma Group’s fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today’s dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.

**Job Description**:
For this project, we are currently searching for a highly experienced QA professional in Biologics to assume the contract with immediate effect. The project will last approximately 4 months and would require as close to 1.0 FTE as possible. In addition, the role requires the successful individual to work site based in Northern Germany with fluency in English and German being a must.

**Responsibilities**
- Overall management of the Quality group and all associated members
- Work closely with internal stakeholders to ensure all regulations are met and objectives of the organisation are achieved
- Strategically develop the goals of the group and implement key changes to ensure the group is both efficient and working to key regulations
- Drive new initiatives related to such areas like digitalization
- Support and participate in Regulatory body audits
- Work closely with team members to ensure any Quality issues are resolved in full to all necessary guidelines
- Lead and support budget planning activities
- Overall leadership of the Quality group ensuring all goals are met

**Qualifications**:

- Must be educated to at least a BSc level in a scientific, engineering or related discipline
- Proven experience in a leadership role ideally working with Biological products
- Strategic and operational skills in Quality Assurance over a substantial period within Biologics
- Thorough knowledge and direct exposure to working to key regulations within the EU and globally (FDA) ideally
- Fluent in English and German
- Can work office based in Northern Germany (staying in the region per week would be sufficient) for at least 3-5 days per week

Additional Information

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.