Freelance Qualified Person

vor 6 Monaten


Berlin, Deutschland ProPharma Group Vollzeit

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Position overview
- Responsibilities include:_- Preparation and authorization of QP- declarations (MIA support)- Support supply chain activities from an advise and expertise perspective- Work with national Regulatory authorities- Support on-going Quality aspects when necessary- Ensure all regulations are maintained and achieved
- Qualifications_- A University degree in Science/Engineering is required, preferably MSc in Pharmacy or similar.- Must have demonstrated experience working as a QP in Germany- Medicinal Cannabis experience is a must- Fluent English and ideally Germany- Already residing in Germany- Can perform the contractual requirements as demonstrated in the Job spec- Strong stakeholder management skills
- 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.



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