CQV Specialist I

AtomVie Global Radiopharma Inc; Hamilton; On-site; CAD 57,600 - 70,400; Full time

Benefits offered by this job

Group Health & Dental Benefits

RRSP Matching Program

Employee Assistance Programs

Job summary

AtomVie Global Radiopharma Inc. in Hamilton, Ontario, is seeking a CQV Specialist to assist the Engineering department with equipment qualifications and compliance. Candidates should have 2-5 years of experience in a GMP pharmaceutical lab setting and knowledge of authority regulations like Health Canada and FDA.

The role involves managing calibration programs, troubleshooting equipment issues, and documenting qualifications. Strong technical skills and communication abilities are essential. The position offers a salary starting at $64,000 annually along with various benefits.

Qualifications

• Minimum of 2-5 years experience in GMP pharmaceutical lab setting.
• Ability to lift 50lbs and work in small spaces.
• Strong understanding of regulatory environments.

Responsibilities

• Manage vendor and internal calibration programs.
• Perform qualification and validation activities.
• Create maintenance programs in CMMS.
• Collaborate with teams for calibration programs.
• Lead investigations of qualification deviations.

Skills

Knowledge of authority regulations

Operating Empower CD

Troubleshooting Waters HPLC systems

Technical report writing

Time management and multitasking

Education

College Diploma in technical field

Tools

HPLC systems

Job description

Salary Range: $64,000.00 To $64,000.00 Annually

AtomVie Global Radiopharma Inc. is a global leading GMP manufacturer and distributor of clinical and commercial radiopharmaceuticals. We work with our partners to transform patients’ lives by advancing high quality drugs for the treatment and diagnosis of diseases.

We are a community that challenges ourselves professionally, takes pride in what we can accomplish together and values the impact we can make with our partners and patients across the globe. Start your career with AtomVie today and help us achieve our vision: to transform lives by revolutionizing healthcare.

About the Role

Reporting to the Engineering Manager as a CQV Specialist, assist the Engineering department focused on laboratory equipment qualifications, calibrations, recertifications, and documentation execution in compliance with GMP practices. This role will also coordinate third-party contractors and contribute to the continuous improvement of the engineering department.

What You Will Do

• Manage and execute vendor and internal calibration & preventive maintenance programs, including the review and approval of service records and reports (e.g., calibration certificates, completed protocols, workorders, and vendor reports) to ensure completeness and accuracy.
• Perform equipment qualification and validation activities across AtomVie. Such as executing HPLC annual qualifications, Gas Chromatograph equipment qualification and balances performance verification and annual calibration etc.
• Create/Develop the lab instrument operational SOP and maintenance programs in CMMS.
• Lead/Support the development and execution of all qualification documentation related to laboratory equipment and software validation.
• Collaborate across teams and locations to ensure calibration programs are implemented and maintained in accordance with cGMPs and the Validation Plan.
• Investigate and troubleshoot problems relating to any CQV tasks. Provide technical assistance during investigations of equipment and validation issues, aid in the resolution of qualification/validation deviations and protocol discrepancies.
• Lead/Support non-conformances related to deviations occurring when equipment fails to meet acceptance criteria.
• Assist or lead the troubleshooting and repair of production and QC related equipment as needed.
• Co‑ordinate with the direct supervisor and technicians to ensure management and QA are informed of compliance status and adherence to commitments.
• Lead and author nonconformancereports, change controls, and CAPAs, ensuring follow‑through to completion within the proposed timeline.

What You Bring to the Role

• Sound knowledge of authority regulations like Health Canada and FDA etc.
• Excellent knowledge of operating Empower CD and operating and troubleshooting on Waters HPLC systems.
• Demonstrated ability to successfully prioritize, manage time well, multitask, and troubleshoot.
• Excellent verbal and written communication skills, with expertise in technical report writing and a strong ability to understand and analyze complex systems and trends.

Requirements

• A minimum of a College Diploma in an technical field (Metrology, Pharmaceutical Sciences etc.), or relevant experience.
• Minimum of 2-5 years hands‑on working experience in GMP pharmaceutical lab setting preferably the Metrology role.
• Ability to lift 50lbs, crawl, stoop, crouch, and kneel in small spaces.

Compensation

Annual salary starts at $64k. Compensation is based on relevant industry experience, academic credentials, and qualifications.

• Group Health & Dental Benefits (from day 1)
• RRSP Matching Program
• Employee Assistance and Wellness Programs

AtomVie does not use artificial intelligence or automated decision-making tools in any part of the recruitment, screening, or selection process.

We are committed to fostering a workplace that values diversity, equity, and inclusion. We believe that a diverse and inclusive workforce enhances our ability to innovate, collaborate, and better serve our clients and patients. We thank you for considering a career with AtomVie. Only those candidates selected for an interview will be contacted. Accommodations are available upon request for candidates taking part in all aspects of the recruitment and selection process. We are dedicated to ensuring that every qualified applicant has an equal opportunity to thrive within our organization.