Scientist 1, Analytical Development
Catalent Pharma Solutions
Summary
Perform laboratory experiments with a high degree of autonomy and communicate project progress to cross-functional teams, management, and clients. Apply creativity and innovation to problem-solving while developing and qualifying analytical test methods for APIs, intermediates, and final drug products.
Job description
The Role
- Perform and train others on analytical techniques including analytical balances, pH meters, high performance liquid chromatography (HPLC/UPLC), UV/Vis spectroscopy, gas chromatography (GC), USP dissolution testing apparatus, moisture analysis by Karl Fischer, disintegration, Pion µdiss, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), particle size distribution (PSD), powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), hardness, and friability testing.
- Develop cleaning verification methods.
- Execute excipient compatibility and forced degradation studies under supervision.
- Troubleshoot and optimize analytical methods for characterization of drug products and intermediates.
- Perform qualification studies to determine if methods are suitable for transfer to Quality Control.
- Independently design and execute simple experiments; seek supervisor input for complex designs.
- Interpret data with limited guidance and identify key factors and findings.
- Maintain clear and accurate laboratory records and review colleagues’ work for accuracy and compliance.
- Engage with clients on technical topics related to their projects.
- Apply strong scientific principles, chemistry knowledge, and proficiency in analytical techniques, Good Manufacturing Practices (GMPs), and technical writing.
- Propose solutions to scientific problems and maintain good housekeeping and safety practices.
- May supervise laboratory assistants.
The Candidate
Minimum Requirements: Four-year degree in a physical, chemical, biological, or pharmaceutical science required. Bachelor’s degree with 1 or more years of experience in analytical development. Master’s degree with experience in analytical development preferred.
Preferred Skills & Background
- Proficiency in analytical techniques including analytical balances, pH meters, high performance liquid chromatography (HPLC/UPLC), gas chromatography (GC), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), gas volume spectroscopy (GVS), UV/Vis spectroscopy, USP dissolution testing apparatus, disintegration, hardness, friability, and moisture analysis by Karl Fischer.
- Highly detail-oriented and organized, with the ability to work independently and collaboratively with a positive attitude.
- Experience using HPLC/UPLC for drug product analysis preferred.
Requirements
- Four-year degree in a physical, chemical, biological, or pharmaceutical science required.
- Bachelor’s degree with 1 or more years of experience in analytical development.
- Master’s degree with experience in analytical development preferred.
- Proficiency in analytical techniques including analytical balances, pH meters, high performance liquid chromatography (HPLC/UPLC), gas chromatography (GC), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), gas volume spectroscopy (GVS), UV/Vis spectroscopy, USP dissolution testing apparatus, disintegration, hardness, friability, and moisture analysis by Karl Fischer.
- Highly detail-oriented and organized, with the ability to work independently and collaboratively with a positive attitude.
- Experience using HPLC/UPLC for drug product analysis preferred.
Benefits
- Paid Time Off
- 10 Paid Holidays
- Medical, Dental & Vision
- Tuition Reimbursement
- Employee Engagement Activities
- Employee Resource Groups
- Wellness Program
- Onsite Fitness Center
- Discounts
Company overview
Catalent Pharma Solutions, now known as Catalent, Inc., is a leading global contract development and manufacturing organization (CDMO) headquartered in Tampa, Florida. Founded in 2007 as a spin-off from Cardinal Health's pharmaceutical technologies segment, the company has grown into a major player in the pharmaceutical services industry. Catalent provides comprehensive drug development and manufacturing solutions including drug delivery technologies, formulation development, analytical testing, clinical and commercial manufacturing, clinical packaging, and supply chain services. The company operates over 50 facilities across four continents and has supported more than half of all FDA-approved products over the past decade. With approximately 16,900 employees, Catalent produces over 70 billion doses annually for more than 8,000 products, serving major pharmaceutical companies like Pfizer, Moderna, Novo Nordisk, and Bristol-Myers Squibb. In 2024, the company was acquired by Novo Holdings A/S for $16.5 billion, further strengthening its position in the global pharmaceutical manufacturing landscape.