Regulatory Affairs Manager Pharmacist

Mvg Recruitment Specialists; Gauteng; On-site; ZAR 200 000 - 300 000; Full time

Job summary

An exciting opportunity awaits a seasoned Regulatory Affairs Manager to lead compliance and product registrations in the pharmaceutical sector. This role involves managing regulatory submissions, liaising with authorities, and mentoring junior staff. If you have a strategic mindset and a passion for quality and compliance, this is your chance to thrive in a dynamic team environment. Join a forward-thinking company where your expertise will play a vital role in bringing medicines to market and ensuring the highest standards of regulatory adherence. Take the next step in your career with this engaging opportunity!

Qualifications

• 5+ years' experience in Regulatory Affairs, preferably with human medicines.
• Strong understanding of product development lifecycle and regulatory compliance.

Responsibilities

• Manage end-to-end regulatory submissions and liaise with regulatory authorities.
• Mentor junior staff and support audits while ensuring compliance.

Skills

Regulatory Affairs

Project Management

Problem-solving

Leadership

Compliance

Education

Degree or diploma in Pharmacy

Tools

CTD/eCTD submissions

Job description

Regulatory Affairs Manager Pharmacist
Location: N JHB
Ref: MVG / RA-NJ

We're Hiring: Regulatory Affairs Manager | Gauteng
Are you a seasoned Regulatory Affairs professional ready to take the lead in ensuring compliance and driving successful product registrations across multiple territories?

An exciting opportunity has opened up for a Regulatory Affairs Manager to join a dynamic team within the pharmaceutical sector.

Key Responsibilities:

1. Manage end-to-end regulatory submissions (new applications & maintenance)
2. Liaise with SAHPRA, other MRAs, and 3rd party partners
3. Allocate resources, set priorities, and ensure compliance with evolving regulations
4. Maintain internal training, mentor junior staff, and support audits/inspections
5. Keep up to date with relevant legislation and regulatory trends

What You'll Bring:

1. A degree or diploma in Pharmacy with SAPC registration
2. 5+ years' experience in Regulatory Affairs (preferably human medicines)
3. Strong understanding of the product development lifecycle
4. Project management expertise and cross-functional collaboration skills
5. Hands-on experience with CTD / eCTD submissions
6. Prior RA Management experience leading a small team

What Makes You Stand Out:

1. Strategic mindset with the ability to work under pressure
2. Excellent leadership, decision-making, and problem-solving skills
3. Passion for quality, compliance, and continuous improvement

If you thrive in a fast-paced, collaborative environment and want to play a key role in bringing medicines to market - this could be the next step in your career.

Interested? Send your CV to response "at" (URL Removed) or apply online.

Desired Skills: Regulatory Affairs, Human Medicines, CTD / eCTD, Product Development Cycle, Project management

Desired Work Experience: 5 to 10 years Pharmaceutical Manufacturing, 5 to 10 years Pharmacist

Desired Qualification Level & Accreditations: Degree, South African Pharmacy Council