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Senior Commissioning/Validation Specialist

Stantec
Posted 4 months ago, valid for 20 days
Location

Cleveland, OH 44193, US

Salary

$107,100 - $202,500 per year

Contract type

Full Time

Tuition Reimbursement
Flexible Spending Account
Wellness Program

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Sonic Summary

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  • Stantec is seeking experienced Commissioning/Validation Specialists to join their Buildings Commissioning/Validation group, focusing on bio-pharmaceutical and nutraceutical facilities.
  • Candidates should have a minimum of 5 years of experience in commissioning and validation tasks related to regulated facilities.
  • The role involves preparing and implementing commissioning/validation plans, reviewing designs, and assisting in project execution while ensuring compliance with specifications and regulatory requirements.
  • Compensation for this position is competitive, with salaries based on individual qualifications, experience, and location, and may include bonuses.
  • Stantec offers a comprehensive benefits package, including medical, dental, vision plans, and a 401(k) plan, along with paid holidays and vacation.

 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.   

Together, we are enhancing the quality of life globally through design. 

Join us and design your place with Stantec. 

Your Opportunity

At Stantec our collaborative team partners with clients at all phases of the project lifecycle to bring to life the designs that support and enhance our communities. The Commissioning and Validation role provides crucial services to confirm equipment and facilities meet the design requirements and produce the expected results. If you are interested in a hands-on role with diverse responsibilities and growth opportunities, we’d be excited to hear from you. We have two immediate openings in our Buildings Commissioning/Validation group for an enthusiastic, diligent and experienced Commissioning / Validation Specialist. In this role you will prepare and implements 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. The commissioning and validation of equipment, facilities, utility systems and computerized systems are intended to verify that they are designed, installed, qualified, and capable of being operated and maintained for performance in conformity with specifications, design intent and client/user and regulatory requirements. Working under the guidance of Director of commissioning/validation, you will work on a variety of projects from small renovations to large complex capital projects across North America.

Your Key Responsibilities

  • Perform commissioning/validation tasks including reviewing shop drawings and equipment submittals, reviewing and/or generating commissioning and validation plans, user requirement specifications, functional and design specifications and other applicable lifecycle documents.
  • 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.
  • Assist in the execution of commissioning/validation project protocols, including discrepancies, and generating final reports to assist in closure of protocols.
  • Assist Director of Commissioning/Validation with client presentations, client contact 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. 

Pay Transparency: In compliance with pay transparency laws, pay ranges are provided for positions in locations where required. Please note, the final agreed upon compensation is based on individual education, qualifications, experience, and work location. At Stantec certain roles are bonus eligible. Actual compensation for part-time roles will be pro-rated based on the agreed number of working hours per week.

Benefits Summary: Regular full-time and part-time employees (working at least 20 hours per week) have access to medical, dental, and vision plans, a wellness program, health saving accounts, flexible spending accounts, 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 and paid family leave. Regular full-time and part-time employees will receive ten paid holidays in each calendar year. In addition, employees will be eligible to accrue vacation between 10 and 20 days per year and eligible for paid sick leave (and if more generous, in accordance with state and local law).

Temporary/casual employees have access to 401(k) plans, employee stock purchase program, and paid leave, in accordance with state and local law.

The benefits information listed above may not apply to union positions because benefits for such positions are governed by applicable collective bargaining agreements



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By applying, a Stantec account will be created for you. Stantec's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.