Senior Commissioning/Validation Specialist

About the role

Stantec’s Buildings team is on a mission to become the world’s leading integrated design practice. Our architects, engineers, interior designers, consultants, sustainability specialists, and technologists are passionate about the power of design. Our collaborative culture and our innovative, sustainable approach to projects help us create buildings that matter to our world. Join us and design your place with Stantec.

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 where drug products are manufactured, stored in GMP conditions and distributed, including computerized and automated systems which require qualification and validation for compliance.
• Review designs, drawings, specifications of facility and equipment and automation to understand project scope and commissioning/validation requirements.
• Prepare commissioning/validation protocols adhering to specifications, client templates and lifecycle documents.
• Affirm and generate final reports to assist in closure of protocols.
• Aid in client presentations, client contact and communication pertaining to specific project deliverables and business development.
• Cook up 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.
• Ability to meet assignment schedule and delivery quality product under pressure.
• Strong interpersonal skills.

Qualifications

• Bachelor's Degree 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

• Proficiency in commissioning and validation processes.
• Knowledge of GMP standards and regulatory requirements.
• Experience with computerized and automated systems.
• Excellent communication and collaboration skills.

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

• Pay Range: $107,100.00 - $160,700.00 Annually.
• Locations in MN, OH, VT, & Various CA, NY Areas.
• Pay Range: $126,400.00 - $189,600.00 Annually.
• Locations in WA, DC & Various CA, MA areas.
• Pay Range: $134,900.00 - $202,500.00 Annually.
• Locations in NYC & CA (Bay Area) & NJ (RP).

Schedule

• Full time.

Travel

• Yes.