Regulatory Affairs Manager SASSA
Quick Summary
Manage regulatory compliance and lifecycle activities for the existing and future portfolio, including submissions, variations,
Pharmacist qualification. Practical understanding of regulatory compliance activities, including submissions, variations, renewals and marketing authorisation lifecycle management.
Requirements
~1 min read- Pharmacist qualification.
- Practical understanding of regulatory compliance activities, including submissions, variations, renewals and marketing authorisation lifecycle management.
- Good computer skills, including Microsoft Word, Microsoft Excel and data management.
- Excellent interpersonal and communication skills for effective collaboration across countries, functions and external stakeholders.
- Strong attention to detail, planning and organisational skills, with the ability to set priorities and assess risk.
- Similar experience from the animal health industry.
- Fluent English.
As Regulatory Affairs Manager SASSA, you will support the maintenance of existing and registration of new animal health products, including therapeutics, feed additives, biocides and care products. Based in Centurion, Gauteng, South Africa, you will provide regulatory, scientific, technical and strategic support, with a strong focus on South African Health Products Regulatory Authority portfolio management and export market growth.
Responsibilities
~1 min read- →Manage regulatory compliance and lifecycle activities for the existing and future portfolio, including submissions, variations, renewals and referrals to the South African Health Products Regulatory Authority and other relevant authorities.
- →Develop and implement regulatory strategies for export markets across the region, while building effective relationships with competent authorities and external regulatory partners.
- →Coordinate packaging development and artwork activities, including the release of production artwork through the Elanco Artwork System.
- →Review and approve promotional materials in PromoMats, and coordinate national regulatory issues, submissions and packaging updates.
- →Maintain regulatory information in systems such as Veeva Vault RIM, collaborate with internal and external stakeholders, and lead regional Regulatory Affairs projects as required.
- Travel: Less than 10%.
- Location: Centurion, Gauteng, South Africa.
Don't meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
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Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
Location & Eligibility
About this job
- Posted
- Today
Listing Details
- Posted
- November 6, 2026
- First seen
- November 6, 2026
- Last seen
- November 6, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 56%
- Scored at
- November 6, 2026
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