About the role
Lab Automation Specialist – Hamilton Systems (Toronto | 100% On-site) Are you hands-on with Hamilton automation systems and ready to join an innovative pharma/biopharma environment? Were hiring a Lab Automation Specialist to lead complex projects, develop robotic protocols (Venus 4+), and integrate diverse software solutions (SoftMax Pro, Green Button Go, Genera, ELN). Your responsibilities: Manage and prioritize automation requests (Kanban, Jira, Scrum) Program and optimize automated workflows (liquid handling) Collaborate directly with scientific and technical teams Mix of technical duties, coordination, and client-facing tasks The profile – MUST HAVES : 3+ years lab automation experience (minimum) Practical, hands-on experience programming Hamilton liquid handling systems Expert with Hamilton systems Proficient with SoftMax Pro plate readers Experience in automating complex workflows Programming skills in Python and/or JavaScript Strong understanding of system integration / data pipelines / SQL or NoSQL Technical context: Pharma, biopharma, analytical QC environment (ELISA/protein assay knowledge is a plus) Automated protocol creation, structured data outputs, continuous improvement Interested or knowing someone who might be interested ? Please send us your resume at alicia.mesplede@efor-group.com.
About PharmEng Technology
PharmEng Technology is a leading global 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.
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 needs and challenges.
At PharmEng Technology, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives and develop 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.
As a trusted partner to some of the world's largest pharmaceutical companies, we have a proven track record of success in delivering high-quality technical services and solutions that drive operational efficiency, reduce costs, and enhance overall performance. We are dedicated to helping our clients succeed in an ever-evolving and highly competitive industry.
At PharmEng Technology, we are passionate about what we do, and we are committed to delivering excellence in everything we do.
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).
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About the role
Lab Automation Specialist – Hamilton Systems (Toronto | 100% On-site) Are you hands-on with Hamilton automation systems and ready to join an innovative pharma/biopharma environment? Were hiring a Lab Automation Specialist to lead complex projects, develop robotic protocols (Venus 4+), and integrate diverse software solutions (SoftMax Pro, Green Button Go, Genera, ELN). Your responsibilities: Manage and prioritize automation requests (Kanban, Jira, Scrum) Program and optimize automated workflows (liquid handling) Collaborate directly with scientific and technical teams Mix of technical duties, coordination, and client-facing tasks The profile – MUST HAVES : 3+ years lab automation experience (minimum) Practical, hands-on experience programming Hamilton liquid handling systems Expert with Hamilton systems Proficient with SoftMax Pro plate readers Experience in automating complex workflows Programming skills in Python and/or JavaScript Strong understanding of system integration / data pipelines / SQL or NoSQL Technical context: Pharma, biopharma, analytical QC environment (ELISA/protein assay knowledge is a plus) Automated protocol creation, structured data outputs, continuous improvement Interested or knowing someone who might be interested ? Please send us your resume at alicia.mesplede@efor-group.com.
About PharmEng Technology
PharmEng Technology is a leading global 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.
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 needs and challenges.
At PharmEng Technology, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives and develop 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.
As a trusted partner to some of the world's largest pharmaceutical companies, we have a proven track record of success in delivering high-quality technical services and solutions that drive operational efficiency, reduce costs, and enhance overall performance. We are dedicated to helping our clients succeed in an ever-evolving and highly competitive industry.
At PharmEng Technology, we are passionate about what we do, and we are committed to delivering excellence in everything we do.
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).