About Our Client: We are a leading pharmaceutical company dedicated to improving the lives of patients through innovative healthcare solutions. With a commitment to excellence and a focus on rare diseases and specialty care, we offer a dynamic and inclusive work environment where you can make a meaningful impact in the healthcare industry.
Position Overview: We are seeking a highly motivated and detail-oriented Regulatory & Quality Assurance Expert to join our growing team in Baar, Switzerland. In this role, you will play a pivotal role in ensuring regulatory compliance and maintaining a high standard of quality for our pharmaceutical products.
Key Responsibilities:
Prepare, submit, and track Market Authorisation (MA) dossiers, including variations, labelling, and safety updates.
Assist in maintaining and enhancing a local quality assurance system in accordance with Swiss legislation and good distribution practice (GDP).
Serve as a Deputy Responsible Person (FvP) and Deputy Local Safety Officer (DLSO).
Support pharmacovigilance obligations and ensure compliance with regulatory guidelines.
Qualifications:
Master\\\'s degree in a medical, pharmaceutical, or science discipline or equivalent.
1-2 years of experience in the pharmaceutical industry.
Demonstrated understanding of regulatory and compliance guidelines, including GDP and GVP.
Native speaker in German, with business fluency in English.
Proficiency in MS Office.
Why Join:
Full Deputy Responsible Person training, offering a clear career path for advancement.
A diverse portfolio spanning rare diseases and specialty care, providing opportunities to expand your regulatory knowledge.
Exciting progression opportunities in line with the company\\\'s growth
ONLY CANDIDATES WITH THE RIGHT TO WORK IN SWITZERLAND CAN BE CONSIDERED\\n \\n \\n \\n \\n \\n
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