About the role
About The Job CSV Engineer Location: Edmonton, Alberta (onsite role)
Client Industry: Pharmaceutical Manufacturing
PharmEng Technology is seeking an experienced Computer System Validation (CSV) Specialist for a 12-month on-site consulting engagement with our client in Edmonton, Alberta. This role is essential in supporting GMP compliance for critical laboratory systems and software in a sterile manufacturing environment.
Key Responsibilities
- Develop and execute validation protocols (URS, FS, IQ, OQ)
- Qualify laboratory and manufacturing equipment (e.g., sterile filling lines, HVAC, HPLC)
- Perform CSV activities in compliance with cGMP and regulatory standards
- Provide hands-on, on-site support and coordination with cross-functional teams
- Maintain documentation, manage deviations, and support audit readiness
Qualifications
- Proven experience in IT Qualification and CSV within GMP-regulated environments
- Strong documentation and validation protocol development skills
- Effective communication and stakeholder coordination capabilities
- Ability to work full-time on-site in Edmonton
About PharmEng Technology PharmEng Technology is a full-service consulting firm providing expert compliance and validation services to the pharmaceutical, biotechnology, and medical device industries. We pride ourselves on delivering high-quality solutions through industry expertise and collaborative client partnerships.
If you're a validation professional looking for your next consulting opportunity, we'd like to hear from you.
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).
About the role
About The Job CSV Engineer Location: Edmonton, Alberta (onsite role)
Client Industry: Pharmaceutical Manufacturing
PharmEng Technology is seeking an experienced Computer System Validation (CSV) Specialist for a 12-month on-site consulting engagement with our client in Edmonton, Alberta. This role is essential in supporting GMP compliance for critical laboratory systems and software in a sterile manufacturing environment.
Key Responsibilities
- Develop and execute validation protocols (URS, FS, IQ, OQ)
- Qualify laboratory and manufacturing equipment (e.g., sterile filling lines, HVAC, HPLC)
- Perform CSV activities in compliance with cGMP and regulatory standards
- Provide hands-on, on-site support and coordination with cross-functional teams
- Maintain documentation, manage deviations, and support audit readiness
Qualifications
- Proven experience in IT Qualification and CSV within GMP-regulated environments
- Strong documentation and validation protocol development skills
- Effective communication and stakeholder coordination capabilities
- Ability to work full-time on-site in Edmonton
About PharmEng Technology PharmEng Technology is a full-service consulting firm providing expert compliance and validation services to the pharmaceutical, biotechnology, and medical device industries. We pride ourselves on delivering high-quality solutions through industry expertise and collaborative client partnerships.
If you're a validation professional looking for your next consulting opportunity, we'd like to hear from you.
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).