Are you passionate about ensuring compliance and regulatory standards within the pharmaceutical industry? Do you thrive in a dynamic environment where your expertise can make a significant impact? If so, we invite you to join a reputable leader in pharmaceutical parallel imports.
Key Responsibilities:
- Oversee regulatory affairs and compliance activities related to pharmaceutical parallel imports.
- Conduct thorough research and analysis of regulatory requirements for imported pharmaceutical products.
- Prepare and submit regulatory documentation to health authorities for product registration and licensing.
- Collaborate with cross-functional teams to ensure compliance with local and international regulations.
- Monitor changes in regulatory requirements and industry trends to proactively address compliance issues.
- Provide regulatory guidance and support to internal stakeholders, including product development and quality assurance teams.
Qualifications:
- Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Regulatory Affairs, or related field. Advanced degree preferred.
- Minimum of 1 years of experience in regulatory affairs within the pharmaceutical industry, preferably in parallel imports.
- Strong understanding of regulatory requirements and guidelines governing pharmaceutical products.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively across teams.
- Detail-oriented approach with a focus on accuracy and compliance.
- Proven ability to manage multiple projects simultaneously and prioritize tasks effectively.
Join us in our mission to deliver high-quality pharmaceutical products while upholding the highest standards of regulatory compliance. Join us and be a part of something extraordinary in the world of pharmaceutical regulatory affairs!