Senior Commissioning/Validation Specialist

About the role

The Commissioning and Validation role provides crucial services to confirm equipment and facilities meet the design requirements and produce the expected results. This role supports diverse projects ranging from small renovations to large complex capital projects across North America.

Responsibilities

• Prepare and implement project commissioning/validation plans for existing or new buildings related to bio-pharmaceutical dosage forms, nutraceutical facilities, and other regulated FDA or similar facilities.
• Review shop drawings and equipment submittals, review and/or generate commissioning and validation plans, user requirement specifications, functional and design specifications, and other applicable lifecycle documents.
• Prepare commissioning/validation protocols adhering to specifications, client templates, and lifecycle documents.
• Affirm execution of commissioning/validation project protocols, including discrepancies, and generate final reports to assist in protocol closure.
• Aid in client presentations, client contacts, and communication pertaining to specific project deliverables and business development.
• Coordinate with other Stantec engineering and client disciplines to confirm alignment with the design intent.
• Recognize when technical problems are developing and escalate or initiate appropriate corrective actions.
• Attend project coordination meetings.
• Support project managers for Commissioning/Validation projects for managing scope and fee for these projects.

Requirements

• Good organizational and time management skills.
• Self-sufficient and self-motivated with strong negotiation skills.
• Strong interpersonal skills.

Qualifications

• Bachelor's Degree in Engineering with an emphasis in Mechanical, Electrical, or Chemical Engineering is preferred, or appropriate combination of relevant education and experience.
• Minimum of 10 years of related work experience.

Skills

• Experience in commissioning and validation of equipment, facilities, utility systems, and computerized systems.
• Knowledge of regulatory requirements for bio-pharmaceutical dosage forms, nutraceutical facilities, and other FDA-regulated facilities.
• Proficiency in project management and coordination.
• Ability to work independently and manage multiple projects simultaneously.

Benefits

• Medical, dental, and vision plans.
• Health savings account.
• Flexible spending account.
• 401(k) plan.
• Employee stock purchase program.
• Life and accidental death & dismemberment (AD&D) insurance.
• Short-term/long-term disability plans.
• Emergency travel benefits.
• Tuition reimbursement.
• Professional membership fee coverage.
• Paid family leave.

Pay

• Range: $107,100.00 - $160,700.00 Annually for some locations.
• Range: $126,400.00 - $189,600.00 Annually for other locations.
• Range: $134,900.00 - $202,500.00 Annually for certain positions.

Schedule

• Full time.