The Scientist III/ Sr. Scientist is responsible for developing and validating analytical methods to support drug formulation development in a GMP-compliant laboratory. This role involves performing validations, stability testing, and forced degradation studies while ensuring data integrity and regulatory compliance. The scientist will independently manage projects, including literature reviews, experimental design, execution, and reporting. Responsibilities also include authoring technical documents such as method validation protocols, development reports, and SOPs, as well as troubleshooting analytical instrumentation like HPLC and GC. Additionally, the role requires mentoring junior scientists, collaborating with cross-functional teams such as Formulation R&D, Quality Control, and Quality Assurance, and maintaining a safe, well-organized laboratory environment.
Direct Reports: No
Indirect Reports: Yes
Key Relationships (examples: Depts or Individual positions that this position will be working closely with):
Travel requirements: N/A
While performing the duties of this job, there may be certain physical demands required for the position.
You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked.

Bringing a topical or transdermal therapy from concept to patient is complex. Scientific uncertainty, regulatory expectations, and manufacturing realities all shape the path forward.
MedPharm supports companies navigating that complexity with focused expertise in topical and transdermal drug development and manufacturing.
From formulation and preclinical research to clinical trial supply and commercial manufacturing, we work alongside partners to advance programs efficiently, strategically, and responsibly.
Our approach is grounded in decades of hands-on experience, advanced research models, and deep regulatory understanding. Every program is different, and our work is tailored to the science and objectives behind each one.
Partnering with MedPharm means working with a specialized CDMO built to de-risk development and translate innovation into commercial reality.