Job Description
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.
💡 Quick Summary
Seeking a career-building opportunity? The CSV Engineer position is now open for candidates interested in the Manufacturing Jobs sector. This role in Edmonton offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Manufacturing Jobs is a plus.
