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ProPharma Group Sweden is hiring a Senior Regulatory Consultant to work on projects from various Pharmaceutical companies. Responsibilities include working on Regulatory Affairs, new registrations/variations, providing local regulatory advice, launch preparations, and collaborating with clients and colleagues. Qualifications include 5+ years of experience in Regulatory Affairs focused on Nordic regulations and an MSc in Pharmacy.

The Cash Application and Collection Team Lead role at ProPharma involves daily cash application, resolving discrepancies, auditing billing and customer set-up, and establishing relationships with customers. The ideal candidate should have strong analytical skills, customer service orientation, and experience with Workday ERP.

Responsible for planning and conducting GVP/GCP audits, acting as a Subject Matter Expert for clinical projects, managing clinical auditing program, and ensuring company compliance to GVP regulations. Also responsible for promoting continual improvement in customer satisfaction and supporting compliance issues within the pharmaceutical industry.

Seeking an independent CSV Engineer with DI experience for a freelance project lasting 12 months. Responsibilities include leading CSV activities, providing guidance on data integrity compliance, authoring validation deliverables, and acting as the subject matter expert in CSV. Must have a B.S./B.A. in Engineering, Science, Information Technology or related field, experience in CSV within the life-science industries, and fluency in English. Position is for a Hybrid approach in Ireland starting on July 1, 2024, for one year.

Seeking a CGT/ATMP Senior Consultant - Qualified Person with 10 years of experience in Biotech and ATMPs. Responsibilities include providing independent consultation on quality assurance and regulatory compliance projects in the Cell & Gene Therapy space. Must have knowledge of manufacturing techniques for cell and gene therapy products in a GMP regulated environment.

The GVP Auditor at ProPharma will lead clinical consulting and auditing projects, ensuring compliance with federal regulatory requirements and ICH guidance. Responsibilities include implementing a risk-based GVP audit program, providing oversight of the GVP consulting program, promoting customer satisfaction, staying updated on industry advancements, and supporting clients and company operations in clinical compliance issues.

The Multilingual Product Integrity Specialist (French) at ProPharma is responsible for evaluating data for product complaints and adverse events, coordinating product retrievals, performing follow-ups, and providing additional services for clients. The role requires excellent English and French language skills, knowledge of medical terminology, and the ability to multitask within strict timelines.