Target Salary Range:
$77,900 Minimum - $103,800 Mid per year (salary to be determined by education, experience, knowledge, skills and abilities of applicant, internal equity, and alignment with market data)
RESPONSIBILITIES- Support and/or lead the management of innovation projects in close collaboration with the business. The focus of the projects will be on the parenteral drug delivery field, in particular on LNPs and the delivery of genetic drugs.
- Support and/or lead the establishment of new formulation capabilities through conducting experiments, characterizing new formulations, and performance testing of new formulations
- Provide thorough tabulation, descriptions, and summaries of experimental methods, data, observations, results, and conclusions both verbally and written.
- Support the maintenance of the designated lab space and applicable equipment
- Perform other duties as assigned
REQUIREMENTS- BSc, MSc, or PhD in Biochemistry, Biology, Chemistry, or Pharmaceutical Sciences
- Work experience: PhD - 0-2 years of work experience in R&D, Formulation or process development, or a related relevant field (pharmaceutical industry experience is an asset)BSc/MSc 3-5 years of work experience in R&D, Formulation or process development, or a related relevant field (pharmaceutical industry experience is an asset)
- Advanced knowledge of the design and development of complex parenteral formulations such as microparticles, polymeric nanoparticles, lipid nanoparticles, polymeric implants, liposomes and micelles. Experience in the field is a plus.
- Knowledge of design and interpretation of pharmacokinetics studies (in vitro and in vivo)
- Experience in the Design of Experiments (DOE) and Quality by Design (QbD) principles for formulation development
- Knowledge of the scientific principles pertaining to and capable in the operation of standard laboratory and/or processing and manufacturing equipment including mixing, emulsification, microfluidics, flow control, drying, hot melt extrusion, spray drying, data collection, etc.
- Knowledge of the scientific principles pertaining to and capable of data interpretation of analytical data including HPLC, UV/Vis spectrophotometry, particle size, IVR, viscometry, DSC, TGA, etc.
- Knowledge and capability of executing documentation requirements associated with pharmaceutical development (e.g. laboratory documentation, development reports, specifications, protocols, batch records, etc.)
- Able to work with minimal supervision in a multidisciplinary team environment
- Must possess strong problem solving, organizational and documentation skills with a focus on details and results
- Good mathematical and computer skills. Proficiency with MS Word, Excel, Power Point and Visio
- The candidate should be self-motivated and possess good interpersonal, collaborative, and communication skills.
Your ApplicationTo ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal. Further information about Evonik as Employer can be found at www.evonik.com/en/careers.html.
Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations.
Your Talent Acquisition Manager:Robin Rose
Company is
Evonik Canada Inc.
