Validation Specialist Overview We are seeking a Validation Specialist to support the qualification and validation of automated manufacturing equipment used in GMP-regulated Life Science environments.

This role is responsible for developing and executing validation activities, creating IQ/OQ/PQ documentation, and serving as the primary validation contact throughout project execution.

Key Responsibilities Develop and execute validation plans, protocols, and reports for automated equipment and production systems.

Perform IQ, OQ, and PQ activities in accordance with GMP and Life Science Validation requirements.

Collaborate with engineering teams to create validation documentation and functional specifications.

Review electrical schematics, drawings, and wiring to verify proper installation and functionality.

Conduct equipment testing for PLCs, HMIs, VFDs, vision systems, instrumentation, motors, and pneumatic/hydraulic systems.

Verify electrical utilities, perform continuity testing, and support troubleshooting activities.

Lead deviation investigations, change controls, and validation documentation updates.

Facilitate internal and customer validation reviews.

Act as the primary validation lead for assigned projects and coordinate validation activities across project teams.

Qualifications Bachelor's degree in Engineering, Physics, Chemistry, Life Sciences, or a related field, or equivalent experience. 3+ years of validation engineering experience in a GMP-regulated environment.

Hands-on experience with IQ/OQ/PQ execution and validation documentation.

Strong understanding of GMP, CQV, and Life Science Validation principles.





Experience working with automated production equipment and PLC-based control systems.

Ability to read and interpret electrical schematics and technical drawings.

Experience with calibration, electrical testing, and industrial control systems.

Strong technical writing, communication, and organizational skills.

Preferred Qualifications Experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing industries.

Experience leading customer-facing validation projects and documentation reviews.

Familiarity with industrial safety systems and machine qualification activities.

Work Environment This position combines hands-on equipment qualification with documentation and project coordination.

The role works closely with engineering, automation, and customer teams in office and manufacturing environments, with occasional travel to customer sites as required.

Job Type & Location This is a Contract position based out of Cambridge, ON.

Pay and Perks The pay range for this position is $35.00 - $50.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity,



and other pertinent job-related factors.

Job Type & Location This is a Contract position based out of Cambridge, ON.

Workplace Type This is a fully onsite position in Cambridge,ON. À propos d'Actalent Actalent est un leader mondial dans les services dingénierie et de sciences ainsi que dans les solutions de talents.

Nous aidons des entreprises visionnaires à faire progresser leurs initiatives dingénierie et de science grâce à laccès à des experts spécialisés qui favorisent léchelle, linnovation et la rapidité de mise sur le marché.

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📌 Validation Specialist (Cambridge)
🏢 Actalent
📍 Cambridge