ProPharma Group
Location
Brasil | Brazil
Job description
Regulatory Consultant - Emerging Markets page is loaded
For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
We're seeking talented Regulatory Affairs Contractors in Brazil, Mexico, South Korea, and other emerging regions to act as a local support for an on-going basis. If you are a competent contractor with experience in local post-marketing activities, we have an exciting opportunity for you to contribute to our success and make a real impact in the pharmaceutical industry.
Join Our Global Network: As a Regulatory Affairs Contractor, you will become a valued member of our global network of experts, working closely with our multinational team of professionals. This collaborative environment offers ample opportunities to learn, grow, and exchange knowledge with industry leaders from various backgrounds and regions.
Your Role: As a competent contractor, you will be responsible for providing expert regulatory support and guidance to our clients in the emerging regions. Your primary focus will be on post-marketing activities, ensuring compliance with local regulations, and maintaining product approvals. You will be involved in activities such as regulatory submissions, labeling updates, variations, life-cycle management, and other critical tasks.
Desired Qualifications: To succeed in this role, we are looking for individuals who possess the following qualifications and attributes:
️ Extensive experience in regulatory affairs within the pharmaceutical industry, specifically in the relevant emerging regions (Brazil, Mexico, South Korea, etc.)
️ In-depth knowledge of local regulatory requirements and guidelines
️ Strong expertise in post-marketing activities, including regulatory submissions, labelling updates, variations, and life-cycle management
️ Proven ability to manage multiple projects simultaneously and meet deadlines
️ Excellent communication skills, both written and verbal
️ Detail-oriented with a strong focus on accuracy and compliance
️ Proficient in English and the local language(s) of the respective region
Please submit your profile to [email protected] to be considered
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
Job tags
Salary
