HiringCafe
Posted 2mo ago

Project / Process Engineer

@ PLZ Corp
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Mississauga, Ontario, Canada
$75k-$85k/yrOnsiteFull Time
Responsibilities:Leads projects, Develops processes, Validates equipment
Requirements Summary:Designs, implements equipment and processes for GMP manufacturing; leads equipment validation, scale-up, and process improvements; ensures regulatory compliance.
Technical Tools Mentioned:AutoCAD, GMP
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Job Description

PLZ is committed to product stewardship and innovation, strong ethical standards, sustainable operations and most importantly, the development of our people. Whether at our manufacturing facilities or corporate headquarters, PLZ prioritizes health and safety, and offers you the support you need to create the career you want, through engagement, equity and inclusion, and opportunity.

From household cleaning solutions to personal care products, and food to automotive lubricants, PLZ produces more than 2,500 different aerosol and liquid products in our facilities across the continent. We know that being the partner of choice for our clients starts with being the partner of choice for our employees. Learn more at www.plzcorp.com/careers or visit https://youtu.be/XYNIFpLQIJY

The Project / Process Engineer is responsible for the implementation of equipment and processes of new manufacturing projects in GMP environment adhering to HC and FDA GMP regulations and follow SOP’s, GMP, GLP and GDP.

Key Responsibility:

  • Leads projects to design, develop, procure and implement new equipment and processes in compounding and filling operations.
  • Monitors technical aspects of manufacturing process and equipment (compounding, mixing and product filling).
  • Evaluates requests for new/changed products and processes and transfer of these to production.
  • Introduce scale-up of new/changed products.
  • Assists in the installation of production equipment.
  • Manages product/production data
  • Qualification and validation of equipment and manufacturing processes as per FDA and HC drug regulations:
  • Writes qualification & validation documents (plans, protocols, & reports).
  • Execute and documents study results for process validation.
  • Conducts cleaning validations.
  • Trains production staff and writes SOPs.
  • Participate in the implementation of preventive maintenance activities related to manufacturing processes
  • Other duties as assigned

 Qualifications:

  • Degree in Chemical Engineering or Mechanical Engineering from a Canadian university or from a university officially recognized as a Canadian university equivalent.
  • Must have knowledge and experience in manufacturing, compounding/mixing and filling processes and equipment for personal care products and OTC , FDA & HC drug GMPs.
  • Practical experience in GMP: HC, FDA 
  • Data Analysis
  • Corrective/Preventative Action Investigation
  • Auditing
  • Drafting utilizing AutoCAD
  • Validation experience in GMP facility

Compensation:

The base pay for this position ranges from $75,000 / year in our lowest geographic market up to $85,000 / year in our highest geographic market. Pay is based on a number of factors including market location and may vary depending on job-related knowledge, skills, and experience. Dependent on the position offered, other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, financial, and/or other benefits.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability, protected veteran status or other protected status. EEOE/M/F/Vet/Disabled. All your information will be kept confidential according to EEO guidelines.