Pharmacovigilance Specialist

Job Title:Pharmacovigilance PharmacistAbout the Role:Curiska is seeking a skilled Pharmacovigilance Pharmacist to oversee product safety and regulatory compliance across Southern and East Africa. The ideal candidate will maintain quality systems, train staff, and manage safety data with a focus on adherence to GxP, ICH, and pharmacovigilance guidelines.Key...

Curiska (Pty) Ltd is seeking a highly skilled Pharmacovigilance Pharmacist to oversee product safety and regulatory compliance across Southern and East Africa.Key Responsibilities:Quality Management: Ensure adherence to GxP, ICH, and pharmacovigilance guidelines. Develop and implement quality systems, train staff on SOPs, and provide SOPs during...

Curiska is seeking a highly skilled Pharmacovigilance Pharmacist to oversee product safety and regulatory compliance across Southern and East Africa. The role involves maintaining quality systems, training staff, and managing safety data.Key Responsibilities:Quality Management: Ensure adherence to GxP, ICH, and pharmacovigilance guidelines. Train staff on...

Job Title: Global Pharmacist Safety SpecialistAbout the Role: Curiska is seeking a skilled Pharmacovigilance Pharmacist to lead product safety and regulatory compliance across Southern and East Africa.Key Responsibilities:Quality Management: Ensure adherence to GxP, ICH, and pharmacovigilance guidelines, train staff on SOPs, and conduct monthly...

Regulatory Affairs Manager Position at CuriskaAs a key member of our team, you will oversee product registration and dossier maintenance in the SEA Cluster, ensuring compliance with regulations and pharmacovigilance requirements. Key responsibilities include leading and managing regulatory strategies, ensuring compliance with regulatory requirements, and...

Job Summary: We are seeking a highly skilled Regulatory Compliance Specialist to join our team at ES Recruitment.Main Responsibilities:Ensure compliance with all relevant regulatory requirements, including Act 101 and Act 53.Prepare and submit regulatory dossiers, including Act 101 and Act 36 submissions.Develop and implement regulatory strategies and...

Hire Resolve is seeking a seasoned Regulatory Affairs Specialist to oversee the regulatory submissions and compliance of pharmaceutical products. This role requires expertise in Human Medicine and Biologicals, ensuring adherence to local and international regulations.Key Responsibilities:Develop and implement regulatory strategies to ensure compliance with...

Key Responsibilities:The successful candidate will be responsible for ensuring regulatory compliance with Act 101 and Act 53.Act as Responsible Pharmacist for the entity.Develop and implement regulatory strategies and plans.Prepare and submit dossiers for regulatory approval.Manage quality and compliance with a focus on quality management system and...

Regulatory Affairs Manager Job DescriptionHire Resolve is seeking a highly skilled Regulatory Affairs Manager to join our client's team. This role involves managing regulatory submissions and ensuring compliance with local and international regulations for human medicine and biologicals.Key Responsibilities:Develop and implement regulatory strategies to...

Regulatory Affairs Manager - Human Medicine and BiologicalsHire Resolve is seeking a seasoned Regulatory Affairs Manager with expertise in Human Medicine and Biologicals to join our client's dynamic team. In this role, you will be responsible for overseeing the regulatory submissions and compliance of pharmaceutical products, ensuring adherence to local and...

Key Responsibilities:Act as Responsible Pharmacist for the entity, ensuring compliance with regulatory requirements.Develop and implement regulatory strategies to ensure successful execution of the regulatory plan.Prepare and submit dossiers, conduct compliance checks, and interact with authorities as necessary.Maintain and manage product life cycles,...

**About Abbott** Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. **Working at Abbott** At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full...

**Job Number** - 70885 **Job Type** - Permanent **Job Title** - Regulatory & Quality Control Specialist **Computer Skills** - Intermediate to Advanced MS Word, Excel, PowerPoint **Industry** - Pharmaceutical **City** - Johannesburg **Province** - Gauteng - This person will also be the Deputy Responsible Pharmacist of the Company.**Summary of...

These customers have new therapeutic ideas but want a partner who can assist with the clinical trial process, the complexities of certain disease states, or other critical capacities. You’ll work with them on the newest treatment breakthroughs for some of the most perplexing conditions. And ultimately, you’ll help make a positive difference in...

**The Position** The Government Affairs Senior Specialist will be responsible for developing and implementing policy and government affairs objectives in a wide range of priorities, healthcare reform, pricing and reimbursement, trade and intellectual property protection and therapeutic area policy. The position will be an integral part of the Government...