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Added 6 mins ago
RB
Senior Product Manager, AI Solutions
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Toronto, ON
- Full-time
Champion a test-and-learn approach, promoting experimentation and the use of data to drive decision-making.
Added 6 mins ago
FB
System Administrator
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- Other
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VE
Senior Project Manager, Electrical Commissioning
Veolia Environnement SA
Edmonton, AB
- Full-time
…leader. It offers a full spectrum of water, waste, and energy management services, including water and wastewater treatment, commercial and hazardous waste collection and disposal, energy…
Added 20 mins ago
AH
Health Information Management Professional I
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AB · Greater Edmonton Metropolitan Area
- Temporary
As a Health Information Management Professional I, you will be responsible for coding and abstracting data from clinical records, releasing information, and performing data quality…
Added 20 mins ago
BS
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Systems Engineer Stf- Integrated Communication and Information System
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Added 50 mins ago
M
Software Engineer - Front End
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Added 50 mins ago
ND
Commercial Operations Officer
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- $9,820.4 CAD / month
- Full-time
A Master’s degree in business, economics, data analytics, technology management or another relevant field.
Added 50 mins ago
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Data Steward (7890EB7)
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- Full-time
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Added 1 hour ago
HT
Researcher – Web Agent
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- Full-time
Prototype new architectures, interaction models, and agent frameworks to empirically test hypotheses and bridge Web capabilities with AI-driven Agents.
Added 1 hour ago
IF
310T Diesel Mechanic
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Added 1 hour ago
IF
310T Licensed Diesel Mechanic Technician
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Added 2 hours ago
BG
Technology, Material and Process Analyst Intern - Placement Year
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Use the knowledge you have learned to interpret the results, generate recommendations and solutions, and learn to create test reports.
Added 2 hours ago
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Technology, Material and Process Analyst - Placement Year
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Goodwood, ON
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…ourselves on providing a friendly, supportive environment and management style, having some great benefits for our employees, career development, progression and work-life…
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…such as interviewing clients and taking history, gathering data appropriate to clinical assessment and diagnosis, involving client in a risk assessment for TB, determining appropriate…
Added 2 hours ago
I
Staff Software Developer, Verified Identity Network
Intuit
Toronto, ON
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Experience developing systems that process data at large scale.
Added 2 hours ago
I
Senior Staff Product Designer
Intuit
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- Full-time
…are a strategic partner who can turn business goals, funnel data, customer insight and brand inputs into design that is distinctive, coherent and built to convert. They know how to pitch…
Added 2 hours ago
G
Software Developer, Google Chat iOS
Google
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- Full-time
…distributed computing, large-scale system design, networking and data storage, security, artificial intelligence, natural language processing, UI design and mobile; the list goes on and is…
Added 3 hours ago
S
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Added 3 hours ago
S
Technical Group Leader
Sanofi
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Added 3 hours ago
SI
IT Senior Analyst, Enterprise Applications - HCM Process & Solutions
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Montreal, QC · Mississauga, ON · Georgetown, ON
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Added 3 hours ago
V|
Process Innovation Co-op
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AtomVie Global Radiopharma Inc.

Quality Control Analyst

Hamilton, ON, Canada

Annual salary starts at $60,000. · Full-time

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Job details

Pay: Annual salary starts at $60,000.
Job type: Full-time
Apply by: Nov 4, 2026
Posting language: English
Posted: Oct 5, 2026

Original 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.

Apply About employer

More about this job

Responsibilities

Perform release and retrospective quality control testing of finished drug products, raw materials, and in-process samples, and coordinate testing with contract laboratories. Document and report results, support investigations and corrective actions, maintain laboratory equipment and supplies, and comply with GMP, nuclear safety, and health and safety requirements.

Requirements

Requires a college diploma or bachelor's degree in Chemistry, Biotechnology, or a related field, plus 1–3 years of relevant experience with analytical chemistry, microbiology, or biology testing. Candidates should be proficient with Empower and common office software, able to write technical reports, and comfortable working shifts and alternating weekends; pharmaceutical GMP, aseptic operations, and Canadian Nuclear Safety Commission experience are assets.

Skills

Analytical Chemistry
Gas Chromatography (GC)
Thin-Layer Chromatography (TLC)
Microbiology Testing
Bacterial Endotoxins Testing
Biology Testing
ELISA
SDS-PAGE
Empower Software
Good Manufacturing Practices (GMP)
Standard Operating Procedures (SOPs)
Technical Documentation
Laboratory Equipment Calibration and Maintenance
Quality Control Testing
Aseptic Operations

Benefits

Group Health and Dental Benefits
RRSP Matching Program
Perkopolis
Employee Assistance and Wellness Programs
Parking Allowance

Visa sponsorship

Not detected in the job text

Keywords

Quality Control
Pharmaceutical Manufacturing
Radiopharmaceuticals
Good Manufacturing Practices (GMP)
Standard Operating Procedures (SOPs)
Analytical Chemistry
Gas Chromatography (GC)
Thin-Layer Chromatography (TLC)
Microbiology
Bacterial Endotoxins
ELISA
SDS-PAGE
Empower
Waters HPLC
Certificates of Analysis
Compendial Testing
USP
European Pharmacopoeia (EP)
Aseptic Operations
Biological Safety Cabinet (BSC)
Canadian Nuclear Safety Commission
Radioactive Material Transfer Forms
Corrective Actions
Non-Conformance Investigations
Excel
Word
Contract Laboratories
Shift Work

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