At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
The Position
A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
The Opportunity
Roche Pharma is seeking a Senior Regulatory Affairs Pharmacist/Associate to join their team in Johannesburg.
Your primary responsibility is to secure the registration of medicines, obtain approval for new product indications in alignment with the business strategy, and maintain current product dossiers.
Key Challenges
Strategic Planning:
Advising on the most suitable time for submitting dossiers/new indications according to Roche Global timeframes and ensuring registration/ approval by the health authority in the shortest possible time.
Coordinate, monitor and supervise timeous submission and maintenance of dossiers in accordance with corporate and local directives, guidelines, SOP’s and legislative requirements.
Gather, analyse and communicate internal and external regulatory intelligence.
Provide regulatory expertise and input into cross-functional Affiliate business strategies (e.g. market access, medical affairs, promotional activities, public policy, technical assessments, technical agreements, local manufacturing/packaging activities, legal issues, etc.)
Develop innovative, risk-based registration plans and submission strategies for Affiliate products with limited guidance from DRA Management.
Operational:
To monitor that Roche Pharma complies with all aspects of local legislation relating to medicines and pharmacy practice as well as other internal guidelines, directives and SOP’s, identify anomalies and implement corrective action.
Review and prioritize the product registration portfolio and align it with the business needs and objectives, in line with market trends and developments.
Compile dossiers and submit in accordance with corporate, legislative and health authority requirements and are executed timeously.
Manage complex or larger scale products to support, take a lead on special projects, and help on-board and train DRA colleagues.
Assist the Product Teams with the approval of advertising materials and reviewing and aligning with the legal advertising requirements
Stakeholder Management:
Provide advice and guidance to relevant Roche departments regarding local medicine, pharmacy legislation and pharmacy practice, internal guidelines, directives and SOP’s.
Support local market access activities from a regulatory perspective
Filings:
Adapt global product dossiers to local requirements.
Prepare and manage regulatory registration filings across product lifecycles.
Monitor and communicate all regulatory filings status and respond to internal and external questions, or other needs
Information and Document Management:
Manage regulatory activities on relevant Roche systems
Review SOPs and compile new and update existing documents in line with requirements
Regulatory Compliance:
Develop and maintain current knowledge of international and local regulations and other governing regulatory practices, policies, procedures, processes, systems and standards.
Prepare for regulatory inspection-readiness
Monitor regulatory compliance for product released to market according to marketing authorisations, identify anomalies and implement corrective action
Manage end-to-end local product packaging and labelling from a regulatory perspective.
Who You Are as an Ideal Candidate
Qualifications & Experience
NQF 8 in Pharmacy or in a Science related field
Must be a registered Pharmacist
5 – 7 years experience in the pharmaceutical environment and/or regulatory environment
You must have knowledge in:
ACT 101 (Medicines control and related
substances Act)
All related medicines regulations
All related guidelines relevant to ACT 101
Quality and Compliance
In the absence of relevant qualifications, experience in the relevant field and at the relevant level will be considered
Recommended skills & abilities
Communication
Planning, organising and prioritising
Analytical thinking
Accuracy and attention to detail
Relationship management
Innovation
Adaptability
Decision making
Physical requirements
Ability to travel nationally and internationally
Who we are
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let’s build a healthier future, together.
Roche is an Equal Opportunity Employer.
