Verified Job
IT / Software / Data Analyst
CSV Engineer
IT / Software / Data Analyst
#688673
Remote / WFH
Job Description
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.
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.
