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Junior Quality Control Consultant

Company

PharmEng Technology

Address Toronto, Ontario, Canada
Employment type FULL_TIME
Salary
Category Pharmaceutical Manufacturing
Expires 2023-10-06
Posted at 8 months ago
Job Description

PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products.


At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals.


We are seeking an experienced Full-time permanent Quality Control (QC) for an on-going project in Toronto, Ontario. Our ideal candidate is a versatile professional with superior skills and experience in optimization of procedure and improvement in on-site or hybrid project-based work environment.


:

  • Contribute to development of project strategy in consultation with supervisor and/or colleagues
  • Work is performed under minimal supervision. Independently determines and develops approach to solution
  • Obtain results or erroneous decisions or recommendations would typically result in program delays and expenditure of resources.
  • Design, execute, and interpret experiments to develop, validate, transfer and troubleshoot quality procedures and test methods. Carries out investigations and produces documentation.
  • Solve assay/process problems.
  • Develop and authors complex, explicit documentation for new and current procedures, validation protocols and technical reports incorporating appropriate use of statistics.
  • Identify potential problems and proactively suggests technical solutions based upon analytical expertise and knowledge of product/process.
  • Represent the organization in providing solutions to difficult technical issues associated with specific projects.
  • Coordinate completion of specific project tasks with other departments.
  • Provide contributions to the understanding and interpretation of results and how they impact the design of subsequent experiments.


Requirements:

  • Technical Skills (including various computer programs and systems)
  • Experience in animal testing
  • Immunology/Biology - BSc with minimum of three (3) years of relevant experience, or MSc with a minimum of one (1) years of relevant experience
  • Outstanding Organization Skills (required to work on multiple projects at the same
  • Experienced in conducting scientific investigations, including OOS investigations and CAPAs
  • Experience in test method development and troubleshooting
  • Outstanding technical writer (protocols, reports, investigations)
  • Experience in performing immunology assays (example: ELISAs and cell-based bioassay methods)
  • Any experience using liquids, soaps, or creams an asset.
  • QC Analytical Excellence skill set should include:



Why PharmEng Technology?

Our consultants come from different areas of the Pharmaceutical/Biotech/Medical Device industries and have extensive experiences obtained from world-class organizations in North America, Europe, and Asia. At PharmEng Technology, we value everyone’s unique talents and work together to support our clients. We offer continuous career growth, competitive wages, opportunities for travel and a team mentality that sets us apart from our competitors. It is the growth of our staff that continues to grow our company globally.


What We Offer:

  • Other great incentives.
  • Comprehensive benefits package & competitive wages.
  • Paid holidays.
  • A supportive environment where employee growth is promoted.


EEOC Statement

At PharmEng Technology, we don’t just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. PharmEng Technology is proud to be an equal opportunity workplace.


Thank you for your consideration and application! We review all resumes and submissions, however, due to the sheer volume of requests that we receive, only successful candidates will be contacted.