Senior CQV Specialist

AtkinsRéalis; Calgary; On-site; CAD 137,000 - 170,000; Full time

Benefits offered by this job

Learning and development opportunities

Competitive pay

Flexible benefits

Defined contribution pension plan

Work-life balance focus

Job summary

AtkinsRéalis is seeking a Senior CQV Specialist to lead technical projects in the pharmaceutical industry, ensuring compliance with regulatory requirements. The candidate will be responsible for documentation, testing coordination, and providing recommendations for equipment optimization. This role offers an exciting opportunity to contribute to major projects and join a company focused on engineering a sustainable future.

Qualifications

• Minimum 8 years relevant work experience.
• Thorough knowledge of cGMP and regulatory requirements.
• Excellent verbal and written communication skills.

Responsibilities

• Provides technical and project leadership in validation processes.
• Develops and reviews technical documentation for clients.
• Coordinates and executes testing of systems and processes.

Skills

cGMP

Validation principles

Statistical analysis

Technical communication

Education

Bachelor’s degree in chemical or mechanical Engineering

Job description

Join to apply for the Senior CQV Specialist role at AtkinsRéalis

Join to apply for the Senior CQV Specialist role at AtkinsRéalis

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Come join us in reshaping the future with AtkinsRéalis. AtkinsRéalis is dedicated in engineering a better future for our planet and its people.

Please note that this job posting aims to create a pool of candidates for future needs.

Your Role Within The Team

• Provides technical and project leadership with a comprehensive understanding of the pharmaceutical industry design/build/validation processes and how they relate to Canadian, EU, and US FDA cGMP regulation requirements.
• Develops/reviews technical documentation for clients in regulated industries including qualification and validation protocols and reports, criticality assessments, risk assessments, validation master plans, user requirements specifications, standard operating procedures and quality plans and policies.
• Coordinate and execute testing of systems and processes from test protocols to assess compliance against requirements.
• Analysis of test data, including that derived from complex processes, and collection of samples, where required.
• Operation of testing equipment.
• Troubleshoots issues of diverse scope where analysis of data requires evaluation of identifiable factors.
• Provide recommendations on equipment/process operation/optimization.
• Provide senior level support to the CQV group to meet department goals and objectives.
  
  

Why choose AtkinsRéalis as an employer?

Because We Offer

• The opportunity to work on various major projects for internal and external clients.
• An exciting environment where work-life balance is important.
• A wide array of learning and development opportunities.
• Competitive pay, flexible benefits, an employee share plan, and a defined contribution pension plan.
• A work environment focused on health and safety.
  
  

The Ideal Candidate

• Bachelor’s degree in chemical or mechanical Engineering or a related Science program.
• Thorough knowledge of cGMP and regulatory requirements for validation.
• Minimum of 8 years relevant work experience which demonstrates knowledge of validation principles, including: validation planning, user requirement and functional specifications, commissioning, IQ, OQ, PQ; with specialized expertise in one or more of the following:
• Qualifying equipment and systems: e.g. incubators, autoclaves, clean utilities, computerized systems, etc.
• Cleaning and process Validation experience.
• Strong knowledge of utilities and general production systems used in pharmaceutical manufacturing.
• Strong working knowledge of statistics and analysis tools.
• Excellent verbal and written communication skills; able to consult/advocate on technical and regulatory issues.
• Proficient in English (oral/written), French knowledge (an asset).
• Must be mobile within the Calgary Area.
  
  

Are you up for this challenge? Apply today and join our team to help engineer a Better Future for our Planet and its People.

At AtkinsRéalis, we seek to hire individuals with diverse characteristics, backgrounds, and perspectives. We strongly believe that world-class talent makes no distinctions based on gender, ethnic or national origin, sexual identity and orientation, age, religion, or disability, but enriches itself through these differences.

AtkinsRéalis cares about your privacy. AtkinsRéalis and other subsidiary or affiliated companies of AtkinsRéalis (referred to throughout as “AtkinsRéalis”) are committed to protecting your privacy. Please consult our Privacy Notice on our Careers site to know more about how we collect, use, and transfer your Personal Data.

By submitting your personal information to AtkinsRéalis, you confirm that you have read and accept our Privacy Notice.

Appropriate accommodations will be provided upon request throughout the recruitment and hiring process as required by Company policy and the Accessibility for Ontarians with Disabilities Act (AODA).

Successful applicants will be notified about AtkinsRéalis’ accommodation policies at the time the employment offer is extended, and the information will be shared with new personnel during the onboarding process.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Information Technology

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