Are you a seasoned Formulation Development professional with a passion for innovation in the generic pharmaceutical sector? ADCAN Pharma, a growing force in pharmaceutical manufacturing, is seeking a highly motivated R&D Specialist to join our dynamic team at our state-of-the-art facility in ICAD III, Abu Dhabi. This is a premier opportunity to advance your career in a strategic and fast-growing market.
About ADCAN Pharma
ADCAN Pharma is a dedicated pharmaceutical manufacturing company committed to enhancing global health by developing and producing high-quality, affordable generic medicines. Located in the industrial hub of ICAD III in Abu Dhabi, we operate under the highest standards of Good Manufacturing Practice (GMP) and compliance. Our focus on Quality by Design (QbD), rigorous research, and cutting-edge technology makes us a leader in the region’s pharmaceutical landscape. We foster a culture of excellence, innovation, and collaboration, empowering our employees to make a significant impact.
Job Description: R&D Specialist
As a key member of our Research & Development team, the R&D Specialist will be instrumental in driving the development of robust generic drug formulations from concept to market. You will be responsible for the entire product development lifecycle, ensuring scientific excellence and regulatory compliance.
Key Responsibilities:
- Lead and execute generic formulation development projects adhering to QbD (Quality by Design) principles.
- Manage and oversee technology transfer activities from R&D to commercial manufacturing scale.
- Prepare and review scientific data and documentation for regulatory market filings across global markets (e.g., UAE, GCC, EMA, FDA).
- Plan, organize, and manage day-to-day research activities to ensure the timely achievement of project milestones.
- Utilize strong troubleshooting capabilities to resolve complex technical challenges during development and scale-up.
- Collaborate effectively with cross-functional departments including Production, Quality Assurance (QA), and Quality Control (QC) in a professional manner.
- Ensure all activities comply with ICH, WHO, EMA, and FDA guidelines, and internal GMP standards.
- Use advanced software systems for data analysis, interpretation, and reporting.
What You Need to Bring (Qualifications & Skills)
Required Qualification:
- Bachelor’s degree or higher in Pharmacy.
- A minimum of 5 years of progressive experience in a Formulation & Development/Technology Transfer department within the pharmaceutical industry.
- Comprehensive knowledge of other pharmaceutical departments and their interplay with R&D.
Preferred Skills and Certifications:
- Professional pharmaceutical license or certification is highly preferred.
- Additional certifications in regulatory compliance are a significant advantage.
- Proficiency in using software and computer systems for pharmaceutical data analysis.
- Strong analytical mind with creative thinking and a detail-oriented attitude.
- Proven ability to work under pressure, achieve strict deadlines, and demonstrate excellent organizational skills.
- Flexibility and a highly motivated, self-starting mentality.
How to Apply
If you are a dedicated professional with the required experience and are excited to contribute to ADCAN Pharma’s mission, we encourage you to apply.
Please submit your updated CV or resume to our HR department at: careers@adcanpharma.ae
