Senior Regulatory Pharmacist

Express Employment Professionals Vaal Triangle; Johannesburg; On-site; ZAR 893,000 - 1,116,000; Full time

Benefits offered by this job

Medical Aid Contribution

Annual Bonuses

Job summary

Express Employment Professionals Vaal Triangle invites a Senior Regulatory Pharmacist to lead regulatory initiatives in a fast-paced pharmaceutical environment in Gauteng. You will ensure compliance, prepare submissions, and guide cross-functional teams on regulatory matters.

The role requires at least five years in pharmaceutical regulatory affairs, a pharmacy qualification, and in-depth knowledge of SAHPRA processes.

Qualifications

• 5+ years in pharmaceutical regulatory affairs.
• Formal qualification in pharmacy or related field.
• Deep understanding of regulatory rules governing pharmaceuticals in South Africa.
• Excellent communication and documentation skills.
• Proven ability to manage multiple projects and meet deadlines.

Responsibilities

• Monitor changes in the regulatory landscape affecting pharmaceutical products.
• Prepare and review technical dossiers for registration purposes.
• Manage and coordinate regulatory inspections and audits.
• Maintain accurate and comprehensive records of all submissions and correspondence.
• Assist in training staff on regulatory compliance standards.

Skills

Regulatory affairs

Pharma compliance

Regulatory submissions

Documentation

Stakeholder communication

Education

Pharmacy degree

Job description

Are you ready to lead regulatory initiatives in a dynamic pharmaceutical environment where collaboration and precision are at the core of everyday success? Our client, a well-established organization in the pharmaceutical industry, is seeking a Senior Regulatory Pharmacist to join their team in Gauteng. This role offers the chance to work in a professional setting that values expertise, integrity, and continuous improvement.

Where You'll Make an Impact:

• Ensure compliance with all regulatory requirements relevant to pharmaceutical products
• Prepare and submit documentation for product registration and variations
• Liaise with regulatory authorities and industry bodies to maintain up-to-date knowledge of legislation
• Support the development and review of internal policies to align with current regulations
• Provide guidance to cross-functional teams on regulatory matters

Duties:

• Monitor changes in the regulatory landscape affecting pharmaceutical products
• Prepare and review technical dossiers for registration purposes
• Manage and coordinate regulatory inspections and audits
• Maintain accurate and comprehensive records of all submissions and correspondence
• Assist in training staff on regulatory compliance standards

Requirements:

• A minimum of 5 years’ experience in pharmaceutical regulatory affairs
• Formal qualification in pharmacy or related field
• Deep understanding of regulatory rules governing pharmaceuticals in South Africa
• Excellent communication and documentation skills
• Proven ability to manage multiple projects and meet deadlines

Familiarity with the following:

• SAHPRA regulations and procedures
• Pharmaceutical product registration processes
• Quality management systems in a pharmaceutical context

Benefits:

• Medical Aid Contribution
• Annual Bonuses

What We’ll Give You:

Join a dedicated team committed to excellence in pharmaceutical regulation. We offer a competitive salary package ranging from R80,000 to R100,000 per month, with a focus on supporting your professional growth and work-life balance. If you are passionate about ensuring the safety, efficacy, and compliance of pharmaceutical products, this is your opportunity to make a meaningful impact.

Take the next step in your regulatory career and contribute to a reputable organization committed to high standards.