Behind every successful organization is a strong and visionary leadership team that genuinely cares about its employees. Our leaders provide support and guidance throughout your professional journey. With their mentorship, expertise, and unwavering support, you'll have the resources and encouragement to overcome challenges and achieve extraordinary results.

Duties & Responsibilities

• Lead and manage pharmacovigilance projects, ensuring adherence to project timelines, budgets, and quality standards.
• Coordinate and collaborate with cross-functional teams, including medical and regulatory to ensure the successful execution of pharmacovigilance activities.
• Oversee the collection, analysis, and reporting of adverse event data, ensuring compliance with regulatory requirements.
• Implement and maintain pharmacovigilance processes and systems to ensure efficient and accurate data management.
• Collaborate internally and externally to ensure proper safety signal detection, evaluation, and risk management.
• Stay updated with relevant regulations, guidelines, and industry best practices to ensure compliance and implementation of the latest pharmacovigilance standards.
• Provide leadership and guidance to team members, fostering a collaborative and productive work environment.

Qualifications & Abilities

• Bachelor’s or advanced degree in pharmacy, life sciences, or a related field.
• Extensive experience in pharmacovigilance within the pharmaceutical industry, with a proven track record of managing pharmacovigilance projects.
• Strong knowledge of global pharmacovigilance regulations, guidelines, and best practices.
• Excellent project management skills, with the ability to effectively prioritize, plan, and manage multiple projects simultaneously.
• Exceptional attention to detail and analytical skills for data analysis and interpretation.
• Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and stakeholders.
• Proficiency in pharmacovigilance databases and systems.

Join our team and contribute to the advancement of patient safety through your expertise in pharmacovigilance project management.

We are seeking a dedicated and experienced Vendor Manager to join our team. As the Vendor Manager, you will play a critical role in managing our relationships with external vendors and suppliers, ensuring the delivery of high-quality services.

Duties & Responsibilities

• Develop and maintain strong relationships with vendors, serving as the primary point of contact for all vendor-related matters.
• Identify and onboard new vendors, conducting thorough evaluations to assess their capabilities, quality standards, and compliance with regulatory requirements.
• Monitor vendor performance and adherence to service agreements (SAs), ensuring timely delivery of goods and services while maintaining quality standards.
• Conduct regular vendor performance reviews and address any issues or concerns, implementing corrective actions as needed.
• Collaborate with cross-functional teams, such as procurement, legal, and quality assurance, to ensure vendor selection and management processes are in line with organizational policies and standards.
• Evaluate vendor risks and implement risk mitigation strategies to minimize any potential disruptions to the supply chain or service delivery.
• Stay updated with industry trends, market dynamics, and regulatory changes that may impact vendor relationships, adjusting strategies and approaches accordingly.
• Maintain accurate vendor records and documentation, including contracts, performance reports, and correspondence.

Qualifications & Abilities

• Bachelor’s degree in business administration, supply chain management, or a related field. Relevant certifications (e.g., Certified Professional in Supply Management) are a plus.
• Proven experience in vendor management, procurement, or supply chain management, preferably within the pharmaceutical or healthcare industry.
• Strong negotiation and contract management skills, with the ability to drive terms and conditions while ensuring compliance.
• Excellent relationship-building and interpersonal skills, with the ability to collaborate effectively with vendors and cross-functional teams.
• Analytical mindset with strong problem-solving abilities, capable of identifying and addressing vendor performance issues or potential risks.
• Exceptional organizational and time management skills, with the ability to prioritize and manage multiple vendor relationships simultaneously.

Join our team as a Vendor Manager and contribute to the success of our organization by establishing and maintaining strong partnerships with our valued vendors and suppliers.

We are seeking a knowledgeable and experienced Regulatory Affairs Manager to join our team. As the Regulatory Affairs Manager, you will be responsible for leading and managing all regulatory activities within our organization to ensure compliance with relevant regulations and guidelines.

Duties & Responsibilities

• Develop and implement regulatory strategies and plans to support the successful registration, approval, and maintenance of our products in accordance with applicable regulations.
• Keep up with the changing regulations and guidelines and assess their impact on our products and operations.
• Prepare and submit regulatory submissions, including but not limited to, marketing authorization applications, variations, and renewals, while ensuring accuracy and completeness.
• Interact and maintain effective relationships with regulatory authorities, acting as the primary point of contact during regulatory inspections, audits, and inquiries.
• Collaborate with cross-functional teams, such a Quality Assurance to provide regulatory guidance and support throughout the product lifecycle.
• Prepare and maintain regulatory documentation, including technical files, dossiers, and labelling materials, in accordance with regulatory requirements.
• Monitor and track regulatory commitments, timelines, and obligations to ensure timely compliance and reporting.
• Stay up to date with industry trends, best practices, and evolving regulatory requirements, and proactively identify opportunities for process improvement and risk mitigation.

Qualifications & Abilities

• Bachelor’s degree in life sciences, pharmacy, or a related field. Advanced degree is a plus.
• Solid experience in regulatory affairs within the pharmaceutical, biotechnology, or medical device industry.
• In-depth knowledge of global regulatory requirements and guidelines, including FDA, EMA, and other relevant authorities.
• Demonstrated experience in preparing and submitting regulatory filings and interacting with regulatory agencies.
• Strong understanding of the drug development process, clinical trials, and post-marketing regulatory requirements.
• Excellent analytical and problem-solving skills, with attention to detail and ability to prioritize and manage multiple projects simultaneously.
• Proven leadership abilities, with the capability to provide guidance, mentorship, and direction to a team of regulatory professionals.

Join us and make a significant impact by leveraging your regulatory expertise to drive regulatory strategies, submissions, and approvals.