Senior CQV Specialist, Pharma Validation Lead

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

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.