Dalton Pharma Services provides contract research and manufacturing services that help companies accelerate their drug discovery and development programs. We provide chemistry support in the area of custom synthesis, process R&D, scale up and hit to lead synthesis including medicinal chemistry with the objective of shortening drug development timelines through the USA. We are strong in small molecule, peptide and oligonucleotide synthesis as well as the manufacture of Active Pharmaceutical Ingredients under cGMP; with scales ranging from mg to small kilos.
We are currently looking to add a Manager for our growing GMP API and Drug Product manufacturing division. An innovative leader with drive is required to bring the medicines of the future into clinical trials and commercial production. Responsibilities include planning and supervising the production of innovative pharmaceuticals in a GMP manufacturing setting in compliance with International Regulatory Requirements.
The role requires strong Project Management skills and the coordination of equipment, materials, manpower and documentation. The management and leadership of a team of dedicated professionals and relevant departments are required to ensure delivery for clinical trials in order to meet client driven timelines and requirements. Responsible for production operations associated with the manufacture of all GMP products, you will develop weekly/monthly objectives as well as schedules, managing activities through line supervisors. You thrive on complexity and will also be responsible for trouble shooting and optimizing the scale up of batch production in a fast paced environment.
With a science degree, in chemistry or Microbiology, you have at least 4 years experience in research and development as well as scale up in a pharmaceutical or biotech GMP manufacturing facility. A self motivated supervisor for a minimum of 3 years, you pride yourself on your ability to hire, motivate and develop high performing teams .The ability to communicate effectively both orally and in writing comes naturally to you; You are organized and have the ability to multi task effectively. Thorough knowledge and understanding of cGMPs and familiarity with FDA guidelines is required.
We offer a competitive salary and benefits as well as an excellent opportunity to build your career with a successful company with a corporate culture based on excellence.
Please forward your resume to:
Human Resources
E-mail: careers@dalton.com
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