Freelance Responsible Person

Requirements

• Qualified Person (QP) / Responsible Person (RP) status in Switzerland
• Familiarity with the Medicinal Products Licensing Ordinance (MPLO)
• Experience working alongside QA teams in a regulatory setting
• Available on short notice when RP cover is required
• Willingness to travel within Switzerland as needed
• All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
• ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

Benefits

Additional Information

For the past 25 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. 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. One of our clients in Switzerland is seeking a qualified Deputy Responsible Person (DRP) in accordance with the Medicinal Products Licensing Ordinance (MPLO). The DRP will step into the Responsible Person (RP) role during periods of absence and collaborate with the client's QA personnel under an agreed communication strategy.

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