- Salary
- C$55k – C$75k/yr
- Location
- Mississauga, ON
- Workplace
- Onsite
- Type
- Full-time
- Department
- Production and Quality
- Source
- Lever
Description
About Us
OTI Lumionics is developing advanced materials—by design—using quantum simulations, machine learning and real-world testing in pilot production. We are currently focused on key enabling materials for OLED displays that will be used in next-generation consumer electronics and automotive. Our advanced electrode materials, and associated manufacturing technology, are being used to build transparent displays and lighting. We work closely with our partners and customers to design new materials that are mass-production ready. Using our computational Materials Discovery Platform, we are able to rapidly iterate new materials, allowing fast turn around time to meet our customers’ needs.
Workplace Type
On-Site
Primary Responsibilities
- Operating production equipment in accordance Standard Operating Procedures (SOPs)
- Performing routine maintenance and calibration of production equipment
- Documenting and reporting batch records accurately and in a timely manner
- Following safety guidelines and maintaining cleanliness on the production floor
- Ensuring adherence to established SOPs when processing, collecting, and packaging product batches
- Maintaining proficiency in the operation and basic maintenance of relevant production equipment
- Assisting in the preparation of procedures, protocols, and reports for new product batches
- Assisting in identifying and implementing processes or equipment changes to improve quality, efficiency, or regulatory compliance
- Supporting the team on various ongoing projects
- Performing all tasks in accordance with established Safe Work Practices and Standard Operating Procedures
- Ensuring compliance with environmental policies, procedures, and objectives, and actively participate in the identification and reduction of environmental impacts related to the role
- Adhering to health and safety protocols, reporting hazards, and contributing to maintaining a safe and healthy work environment for all employees
- Performing other ad hoc duties as assigned
Profile
- Post-Secondary Degree in Science/Engineering or equivalent combination of education and experience
- Minimum of two (2) years of hands-on experience in a manufacturing, pharmaceutical and/or GMP regulated facility
Required Skills
- Familiarity with pharmaceutical regulations
- Knowledge of current Good Manufacturing Practices and the ability to follow Standard Operating Procedures
- Highly developed mindset of quality, regulatory and production
- Detail oriented and well organized, with a high degree of accuracy and thoroughness
- Excellent interpersonal and communication skills
- Ability to multi-task, meet tight timelines in a fast-paced environment
- Proven problem-solving abilities
- Proficiency with Microsoft Office
- Ability to independently lift up to 8 kg confidently
- Willingness to work extended hours as required
- Ability to work all shifts, including morning and evening shifts, weekends, and holidays
- The following will be considered as an asset
- Cleanroom experience
- Experience operating vacuum equipment
Skills
Machine LearningGMPCompliance
