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Posted 2 months ago

QC Analyst

@ AtomVie Global Radiopharma Inc.

Hamilton, Ontario

$60k/yrFull-time1+ years experience
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SIGNALS

Overview

AtomVie Global Radiopharma Inc. is hiring a full-time QC Analyst in Hamilton, ON, onsite, to perform release and retrospective quality control testing on finished drug products, raw materials and in-process samples under GMP and CNSC rules. The role includes documentation, equipment calibration, inventory, training support and shift work with alternating weekends. Salary starts at $60,000 per year, based on experience and credentials.

Pay:

From $60,000 a year

Responsibilities:

  • Perform release and retrospective QC testing of drug products and raw materials
  • Document analytical data and write certificates of analysis and test reports
  • Calibrate and maintain laboratory equipment
  • Maintain reagent, reference standard and consumable inventory
  • Report deviations and assist with investigations and corrective actions

Requirements summary:

  • College diploma or B.Sc. in chemistry, biotechnology or related field
  • 1 to 3 years of analytical chemistry or microbiology lab experience
  • Proficiency with Empower, Excel and Word
  • Good English communication and teamwork
  • Ability to lift up to 23 kg
  • Shift work and alternating weekends

Tools & skills

Benefits mentioned

Health insuranceDentalRetirement planEmployee assistanceWellness
Source and dates

Employer career site / ATS feed · adp

Employer posting date
2026-09-04
First seen by our source
2026-10-10
Source record updated
2026-10-27

These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.

Job details

SeniorityEntry level
DepartmentQuality assurance
Experience1+ years
Hours per week40 (estimated)
Scheduleweekends
Travelair: none · ground: none
Work settingLaboratory, Warehouse
PositionSitting and standing
Physical demandsphysical moderate · lift 50 lb · computer moderate
LanguagesEnglish
EducationCollege diploma (required), Bachelor’s degree (required)
Fields of studyChemistry, Biotechnology
Perks mentionedRetirement plan, Wellness, Transit support, Home office allowance

Summary and details written by AI from the posting; the employer’s posting is the authority.

AtomVie Global Radiopharma Inc.

Saved company profile

Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.

Empowering Next Generation Radiotherapeutics

Full company description

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].

LinkedIn followers
24,012
People associated on LinkedIn
156
Reported office locations
  • 10 Aeropark Blvd, Hamilton, Ontario L0R 1W0, CA
  • 1280 Main St. W, NRB-A316, Hamilton, Ontario L8S 4K1, CA
Business categories
  • Medical Device
  • Manufacturing
Other recorded names
  • AtomVie Global Radiopharma
  • AtomVie Global Radiopharma Inc.
Profile identifies a recruitment agency
No
Reported total investment
130,000,000

Currency and observation date were not supplied; this is not a current valuation or a funding round.

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…

FieldValue
IndustryPharmaceutical Manufacturing
Company size51-200 employees
HeadquartersHamilton, Ontario
Organization typePrivately Held
Open jobs on Jobsy12
LinkedInView page
Job description

As a QC Analyst, you will be responsible for working in accordance with company policies and within GMPs while contributing your technical expertise to support current products and develop future drugs within the AtomVie portfolio.

This posting is for an existing vacancy to support the expansion of the company.

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

What You Will Do

  • Perform quality control (release & retrospective) testing of finished drug products, raw materials and in-processing testing according to standard testing methods (STMs) which may either be compendial or developed/validated in-house; technique areas include analytical chemistry, biology and microbiology.
  • Conduct all work in accordance with AtomVie Standard Operating Procedures (SOPs) and raise any deviations immediately to the attention of Lab Management and Quality Assurance. Report testing failure and non-conformances (both orally and in written), assist in conducting investigations and implement corrective actions with supervision.
  • Proper documentation of analytical data and information.
  • Write technical documents (e.g. generate Certificate of analysis, test reports, data summaries, etc.).
  • Perform calibration/maintenance of fundamental lab equipment.
  • Responsible for maintaining inventory of analytical reagents, critical material, reference standard and laboratory consumables.
  • Responsible for maintenance of documentation to fulfill applicable regulatory requirements relating to nuclear safety (e.g. radioactive material transfer forms).
  • Responsible for the housekeeping in accordance with AtomVie Standard Operating Procedures (SOPs).
  • Coordinate quality control (release &retrospective) testing of drug substances with contract laboratories or contract research organizations according to standard testing procedures, USP or EP.
  • Plan, implement, and successfully complete assigned tasks in a timely fashion ensuring consistent high quality.
  • Liaises with higher level laboratory personnel to learn the use of all applicable physical & chemical testing equipment and to acquire a fundamental understanding of departmental and regulatory practices.
  • Assist in training of other colleagues.
  • Ensure compliance with Health and Safety for all policies, procedures and regulations applicable to their work.
  • Adhere to Canadian Nuclear Safety Commission.
  • Adhere to GMP regulations.
  • Complete all other related duties assigned.

What You Bring to the Role

  • Basic understanding and ability to follow test methods/SOPs/compendia and Certificates of Analysis.
  • Ability to make routine decisions around simple task priorities but governed strictly in their work by SOPs. Typically seeks the input of higher-level team members in non-routine matters.
  • Ability to work in a safe manner collaborating as a team member to achieve all outcomes.

Requirements

  • College Diploma or B.Sc. in Chemistry, Biotechnology, or a related field.
  • 1 to 3 years of related experience in analytical chemistry techniques such as HPLC, GC and TLC, microbiology tests such as Bacterial Endotoxins, and/or Biology tests such as IRF, ELISA and SDS-PAGE.
  • Proficiency with equipment data processing software such as Empower (Waters HPLC).
  • Proficiency with spreadsheets (e.g. Excel), word processing software (e.g. Word) and ability to write technical documents and reports.
  • Good communication skills (in English) and ability to work both independently and cooperatively in a team environment.
  • Experience in a pharmaceutical cGMP environment, experience in aseptic operations (use of a BSC - Biological Safety Cabinet) and working under Canadian Nuclear Safety Commission regulations are assets in this role.
  • This position requires shift work and alternating weekends.
  • Ability to lift and move heavy weights up to 23 kilograms is required.

Compensation:

Annual salary starts at $60,000. 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.

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