At Adalvo, we're not just a company - we're a team of passionate people driven by our mission to consistently deliver high-quality products and services to our partners.
We are positive, we are fast, we are always on target, we are Adalvo!
We are looking for an enthusiastic R&D Manager to join our dynamic Adalvo team.
This position offers an opportunity to well-suited candidates to join a growing, fast paced energetic environment and culture.
This is a temporal role of 6 months to cover a maternity leave.
Summary of the role
- Hands on execution of the development programs and tech transfer of the new products - with a strong focus on the high-potent drugs, e.g., oncologic drugs, in target finished dosage forms.
- Together with the respective R&D team plan and elaborate on scientifically sound experimental development activities, and lead their execution, data interpretations and technical conclusions.
- Establish a strong relationship with key internal and external partners by regular technical meetings (remotely and face to face).
- Provide specification for API, Raw and packaging materials to support supply chain in the identification of suitable supplier.
- Facilitate the resolution of technical issues in a timely manner, driving action items and follow up.
- Manage and support DP validation activities.
- Create intellectual property covering pharmaceuticals products.
- Support internal and external functions to ensure a smooth transfer of technologies and products into additional commercial manufacturing site (if required).
- Ensure accurate tracking and reporting of project deliverables and milestones, maintaining consistent project documentation and preparing periodic updates for the Senior Management.
- Actively assist other department team members in reviewing documents on other projects (protocols, reports, regulatory filings, specifications, and the like).
- Establish effective working relationships within other key with internal and external cross-functional teams, e.g., PMO, RA, Intellectual Property, Production and Quality Assurance & Control.
Qualifications and requirements
- BS/MS in Pharmacy or Pharmaceutical Technology with 8 years of industrial Drug Product development experience for highly regulated markets.
PhD is an asset.
- Hands on experience and expertise in the pharmaceutical development of oral dosage forms and topicals.
At least 3 years of experience on development with high-potent drugs is highly desirable.
- Experience with EMA, FDA, ANVISA and other regulated markets with understanding of regulatory requirements.
- Experience in management of high-performing R&D team.
- Able to demonstrate strong attention to detail while working under pressure.
- Ability to communicate and connect with all levels of the organization.
- Strong leadership and resource management skills.
- Excellent English written/oral communication skills are required.
Why join us?
Exciting Challenges: Every day brings new opportunities to learn and grow.
Supportive Environment: We foster a culture of collaboration, where your ideas are valued, and your voice is heard.
Career Development: We're committed to helping you reach your full potential through ongoing training and development opportunities.
Recognizing Excellence: We recognize and appreciate hard work and dedication by offering competitive compensation packages and employee rewards programs that acknowledge contributions and achievements.
Fun and Inclusive Culture: We believe in celebrating our successes and building strong connections within our team.
Ready to Ignite Your Passion?
If you're ready to take the next step in your career and join a business committed to consistently deliver high-quality products and services, then we want to hear from you!
Apply to the role with your resume attached!
Please be informed that only selected candidates will be contacted.