Clera home
·Dashboard

Jobs at AtomVie Global Radiopharma Inc. (Now Hiring) — 2 open

AtomVie Global Radiopharma Inc. logoAtomVie Global Radiopharma Inc.

CQV Specialist I

Hamilton, Ontario, Canada · On-site

Mid level$130M raised

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…

Skills: Equipment Qualification, Calibration, GMP Compliance, Empower CDS, Waters HPLC Systems

AtomVie Global Radiopharma Inc. logoAtomVie Global Radiopharma Inc.

QC Analyst

Hamilton, Ontario, Canada · On-site

$60k/yr

Mid level$130M raised

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…

Skills: HPLC, GC, TLC, Bacterial Endotoxins Testing, IRF

AtomVie Global Radiopharma Inc. logo

CQV Specialist I

AtomVie Global Radiopharma Inc.

Hamilton, Ontario, Canada • On-site

Apply
Mid level

Tired of cold applications?

Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.

  • Full-time
  • associate degree
  • Group Health & Dental Benefits, Rrsp Matching Program, Perkopolis, Employee Assistance and Wellness Programs, Parking Allowance
  • Posted 15d ago
  • ~40 hrs/week

Responsibilities

The CQV Specialist assists the Engineering department with laboratory equipment qualifications, calibrations, and documentation in compliance with GMP practices. This includes managing calibration programs, executing validation activities for HPLC and Gas Chromatography, and authoring non-conformance reports and CAPAs.

Requirements

Requires a minimum of a College Diploma in a technical field such as Metrology or Pharmaceutical Sciences. Candidates must have 2-5 years of hands-on experience in a GMP Pharmaceutical lab setting, preferably in a metrology role.

Full job description

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

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. .

Location: AtomVie Global Radiopharma Inc, Hamilton ON (Onsite).

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, work orders, and vendor reports) to ensure completeness and accuracy
  • Perform equipment qualification and validation activities across AtomVie. Such as executing HPLC annual qualifications, Gas Chromatography 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 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.
  • Excellent knowledge of operating Empower CDS 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 a 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.

AtomVie Offers

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

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.

Related keywords

CQVGMPRadiopharmaceuticalsHealth CanadaFDAEmpower CDSWaters HPLCGas ChromatographyMetrologyValidation PlanCAPAChange ControlSOPCMMSCalibration CertificatesPharmaceutical Sciences

About AtomVie Global Radiopharma Inc.

LinkedInVisit site

Empowering Next Generation Radiotherapeutics

Industry
Pharmaceutical Manufacturing
Company size
51-200 employees
Headquarters
Hamilton, Ontario
LinkedIn followers
23,812
Total funding
$130M

AtomVie Global Radiopharma Inc. ("AtomVie"), incorporated in late 2021, is a global leading CDMO for the GMP manufacturing and distribution of clinical and commercial radiopharmaceuticals and the most recent spinout from the Centre for Probe Development and Commercialization (CPDC). AtomVie offers the full range of scientific, technical, regulatory, quality, logistics and business expertise combined with a specialized infrastructure for the development of your radiopharmaceuticals from Phase 1 to the commercial marketplace. With a state-of-the art purpose-built facility that will be operational in Q4 2025, AtomVie empowers the development of your radiotherapeutics. For more information about AtomVie, visit our website or contact: [email protected].

Offices: 10 Aeropark Blvd, Hamilton, Ontario L0R 1W0, CA · 1280 Main St. W, NRB-A316, Hamilton, Ontario L8S 4K1, CA

Medical DeviceManufacturing
View all jobs at AtomVie Global Radiopharma Inc.

About AtomVie Global Radiopharma Inc.

LinkedInVisit site

Empowering Next Generation Radiotherapeutics

Industry
Pharmaceutical Manufacturing
Company size
51-200 employees
Headquarters
Hamilton, Ontario
LinkedIn followers
23,812
Total funding
$130M

AtomVie Global Radiopharma Inc. ("AtomVie"), incorporated in late 2021, is a global leading CDMO for the GMP manufacturing and distribution of clinical and commercial radiopharmaceuticals and the most recent spinout from the Centre for Probe Development and Commercialization (CPDC). AtomVie offers the full range of scientific, technical, regulatory, quality, logistics and business expertise combined with a specialized infrastructure for the development of your radiopharmaceuticals from Phase 1 to the commercial marketplace. With a state-of-the art purpose-built facility that will be operational in Q4 2025, AtomVie empowers the development of your radiotherapeutics. For more information about AtomVie, visit our website or contact: [email protected].

Offices: 10 Aeropark Blvd, Hamilton, Ontario L0R 1W0, CA · 1280 Main St. W, NRB-A316, Hamilton, Ontario L8S 4K1, CA

Medical DeviceManufacturing
View all jobs at AtomVie Global Radiopharma Inc.

Similar companies hiring

Johnson & Johnson Innovative Medicine (1239)MSD (921)AstraZeneca (754)Novartis (662)Sanofi (555)Takeda (490)Grifols (383)GSK (337)Eli Lilly and Company (316)Catalent (287)Boehringer Ingelheim (276)Viatris Connect (270)
Clera home

Your AI-talent agent. Connecting talents with dream jobs.

Earn $5,000

Tools

  • Salary Calculator
  • Resume Review
  • Startup Map

Explore

  • Jobs
  • Discover Jobs
  • Companies
  • Acquihire
  • Referral

Company

  • Manifesto
  • Engineering
  • We are hiring!
  • FAQs
  • Blog
  • Press

Tools

  • Salary Calculator
  • Resume Review
  • Startup Map

Explore

  • Jobs
  • Discover Jobs
  • Companies
  • Acquihire
  • Referral

Company

  • Manifesto
  • Engineering
  • We are hiring!
  • FAQs
  • Blog
  • Press

© 2026 Clera Labs, Inc.

PrivacyTermsBug Bounty