PharmEng Technology is a global leader in providing innovative technical services, specializing in commissioning, qualification, and validation for the pharmaceutical and biotechnology industries.
Toronto, Ontario
PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes. As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players. Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges. At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs. Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).
On-site
The CQV Engineer will support the preparation, execution, and review of commissioning, qualification, and validation protocols for pharmaceutical and biotech systems. They will collaborate with cross-functional teams to perform functional testing, manage punchlists, and ensure compliance with GMP standards.
On-site · Toronto
The Lab Automation Specialist will manage and prioritize automation requests while programming and optimizing liquid handling workflows. They will collaborate with scientific teams to integrate software solutions and ensure continuous improvement of automated protocols.
Remote · Toronto, Ontario, Canada
The Documentation and IV Execution Lead is responsible for managing the lifecycle of CQ documentation within the Kneat platform and ensuring technical and GDP compliance. They will lead IV execution, coordinate with multidisciplinary teams, and support project controls through progress reporting and schedule management.
On-site · Toronto
The CQV Engineer is responsible for executing Design, Installation, and Operational Qualifications, including attending FATs and performing system walk-downs. They ensure all installations comply with design requirements and manage the closeout of punchlist items and change controls.
Hybrid · Toronto
Own the end-to-end operational and compliance management of multi-state US payroll, including federal and state tax filings. Serve as the subject matter expert for payroll systems implementation and internal stakeholder coordination.
