MedPharm Ltd is a leading CDMO specializing in the development and manufacturing of topical and transepithelial therapies. With over two decades of experience, they offer comprehensive services including formulation development, clinical trial supply manufacture, and high-potency capabilities. MedPharm stands out by combining cutting-edge research with deep regulatory expertise to deliver tailored solutions that ensure patient success worldwide.
Open Positions
IT Operations Intern
Rising junior or senior, strong interest in IT, basic familiarity with Windows and networking concepts
GMP Technician
GCSEs or equivalent, experience in regulated environments, and ability to work effectively in a team
Production Director
Bachelor's degree in Engineering, Life Sciences, Manufacturing, or a related field, 5+ years of leadership experience, 8+ years manufacturing experience in a cGMP setting for pharmaceuticals
Associate Scientist, Analytical
Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences or related discipline, familiarity with analytical equipment and instrumentation, and computer literacy in Microsoft Office Applications
Associate Scientist, Analytical
Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences or related discipline; familiarity with common analytical equipment and instrumentation
Study Director/Senior Scientist
3-5 years of experience, Bachelor's degree in a relevant scientific field, and proficiency in technical writing
Director, Business Development East Coast
10+ years of experience in pharmaceutical industry with B.S. in Pharmaceutical Sciences, Chemistry, or related discipline
QC Manager, Raw Materials
5+ years of supervisory experience in Quality Control or Analytical development, Bachelor's degree in a scientific discipline
QA Systems Manager – eQMS & CSV
Bachelor’s degree in Life Sciences, Engineering, Computer Science, or related discipline, with 5 years of experience working in the pharmaceutical industry and training in Computer System Validation
Process Technician
A.A.S. in a scientific discipline, 2-4 years' experience in a cGMP biopharmaceutical manufacturing environment, and ability to work in a rapidly changing environment
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