Job Description
Our client develops and manufactures novel innovative dosage forms and solutions to its customers in the health care industry. The company’s solves customers’ most pressing product development challenges, including bioavailability enhancement, modified release, abuse deterrence, biotherapeutics processing, and inhalation formulation.
The role holder is responsible for the management of formulation development projects & supervision of clinical manufacturing. The role will lead platform formulation research initiatives. The candidate will have a pharmaceutical background & experience within a cGMP, FDA and MHRA regulated environment. The company have multiple technologies including IP protection, solutions for immediate & controlled release, colonic delivery (small molecules, proteins and peptides) & combination products.
The role demands an MSc or PhD in pharmaceutical sciences or related subjects and at least 3 years relevant industry experience and ideally 5 years direct technical experience of formulation and drug delivery within the industry
Experience in oral solid dosage forms and delivery systems is required along with experience of product development within a pharmaceutical environment with formulations of drug products for pre-clinical and clinical trials.
A track record of innovative problem solving in pharmaceutical development is required. Knowledge of pharmaceutical development process and relevant regulatory guidelines together wiith and experience of working within a cGMP environment.
