CQV Specialist I (Manufacturing Systems)

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

Benefits offered by this job

Health & Dental benefits (from day 1)

RRSP matching

Wellness programs

Job summary

AtomVie Global Radiopharma Inc. in Hamilton, ON is seeking a CQV Specialist I (Manufacturing Systems) to support the Engineering team with qualification, calibration, and documentation in line with GMP practices.

You will coordinate third-party contractors, develop SOPs and CMMS maintenance programs, and drive CQV activities across equipment such as isolators, RABS, cleanrooms, and fume hoods, ensuring production schedules and quality standards are met.

Qualifications

• College Diploma in a technical field (Pharmaceutical Sciences, Mechanical, Mechatronics etc.,) or relevant experience.
• 2-5 years hands on working experience in Pharma or food manufacturing facility in a technical capacity.
• Ability to lift 50lbs, crawl, stoop, crouch, and kneel in small spaces.
• Knowledge of Health Canada and FDA regulations is preferred.

Responsibilities

• Perform CQV qualification and validation activities across AtomVie (e.g., Cleanrooms, Isolators, Hot cells, RABS, BSCs, fume hoods).
• Manage and review qualification protocols and reports for completeness and accuracy.
• Collaborate across teams to implement qualification programs per cGMPs and Validation Plan.
• Develop equipment operating SOPs and CMMS maintenance programs.
• Lead/Support CQV documentation (IQ/OQ/PQ) and address deviations.

Skills

Prioritization

Multitasking

Troubleshooting

Communication skills

Education

College Diploma in a technical field

Tools

Isolators

RABS

Job description

CQV Specialist I (Manufacturing Systems)

Full Time Hamilton, ON, CA

9 days ago Requisition ID: 1410

Salary: $64,000.00 Annually

AtomVie Global Radiopharma Inc. is a global leading GMP manufacturer and distributer 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

TheCQV Specialist (Manufacturing Systems) will assist the Engineering department focusing on manufacturing 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. The primary objective is to support CQV activities in alignment with standards and AtomVie’s requirements.

What You Will Do

• Perform equipment qualification and validation activities across AtomVie. Such as executing Cleanrooms, Isolators, Hot cells, RABS, Biological safety cabinet, fume hoods performance verification and qualification etc.
• Manage and execute vendor and internal qualification and certification programs, including the review and approval of qualification protocols and reports to ensure completeness and accuracy
• Collaborate across teams and locations to ensure qualification programs are implemented and maintained in accordance with cGMPs and the Validation Plan
• Create/Develop the equipment operating SOPs and maintenance programs in CMMS.
• Co-ordinate with the production teams to ensure that re-qualification activities do not impact on their schedules.
• Lead/Support the development of (IQ/OQ/PQ) qualification documents as required and execution of all qualification documentation related to manufacturing equipment and software validation.
• 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
• Demonstrate safety knowledge, awareness and compliance with all safety and other job-related policies and procedures.
• 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.
• Participating in compulsory training is deemed necessary for the role.
• Ensure compliance with Health, Safety and Environment protection rules, with engagement of all associates to apply the policies, procedures and regulations applicable to their work.
• Demonstrate safety knowledge, awareness and compliance with all safety and other job-related policies and procedures
• Lead and author nonconformance reports, 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.
• knowledge of Isolators / RABS is an added Asset.
• 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 a technical field (Pharmaceutical Sciences, Mechanical, Mechatronics etc.,) or relevant experience.
• Minimum Two (2) to five (5) years hands on working experience in Pharma or food manufacturing facility in a technical capacity.
• 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.