Posted last month
QA - Data Reviewer, Associate
@ AtomVie Global Radiopharma Inc.
Hamilton, Ontario
Overview
AtomVie Global Radiopharma Inc. is hiring a QA Data Reviewer, Associate in Hamilton, Ontario, onsite, to verify the integrity of analytical records for radiopharmaceuticals. The role reviews data from HPLC, GC, TLC and pH meters, audit trails and out-of-specification results, and requires flexibility for a 24/7 operation. Compensation starts at $70,000 per year.
Pay:
From $70,000 a year
Responsibilities:
- Review analytical data from HPLC, GC, TLC and pH meters
- Verify completeness of sampling, preparation and reportable result records
- Review equipment audit trails as prescribed by SOPs
- Contribute to out-of-specification and out-of-trend investigations
- Mentor laboratory staff on data integrity and GDP
Requirements summary:
- Post-secondary education in engineering, chemistry, microbiology or related field
- Minimum 5 years of analytical testing or data review in pharma or radiopharma
- GMP environment experience required
- Working knowledge of data integrity, GDP and 21 CFR Part 11
- Excellent written and oral English communication
Tools & skills
Benefits mentioned
Source and dates
Employer career site / ATS feed · adp
- Employer posting date
- 2026-10-02
- First seen by our source
- 2026-10-10
- Source record updated
- 2026-11-03
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Entry level |
| Department | Quality assurance |
| Experience | 5+ years |
| Hours per week | 40 (estimated) |
| Schedule | overnight |
| Travel | air: none · ground: none |
| Work setting | Laboratory, Office |
| Position | Sitting and standing |
| Physical demands | physical low · computer high |
| Languages | English |
| Education | Bachelor’s degree (required) |
| Fields of study | Engineering, Chemistry, Microbiology |
| Perks mentioned | Retirement 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…
| Field | Value |
|---|---|
| Industry | Pharmaceutical Manufacturing |
| Company size | 51-200 employees |
| Headquarters | Hamilton, Ontario |
| Organization type | Privately Held |
| Open jobs on Jobsy | 12 |
| View page |
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
The QA – Data Reviewer, Associate is responsible for ensuring GMP compliance and data integrity through verification of records generated in sampling, preparation, instrumental analysis, data evaluation and calculation of reportable results related to radiopharmaceuticals at AtomVie. This role is critical in sustaining data integrity principles in Analytical Development and Quality Control laboratories operating at AtomVie.
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
- Reviews data carried out using a wide variety of equipment including but not limited to HPLC, GC, TLC, and pH meters
- Reviews the completeness of the records generated in sampling, preparation, instrumental analysis, data evaluation and calculation of reportable results to verify integrity of all data generated and reported
- Ensure the test methods, protocols and Standard Operating Procedures (SOPs) were followed by chemists, scientists and biochemists
- Conducts and documents periodic review of audit trails in the variety of equipment as prescribed by internal SOPs
- Contributes to laboratory investigations of Out of Specification and/or Out of Trend results
- Works collaboratively with stakeholders to ensure the data meets ALCOA+ integrity
- Provide guidance and support to laboratory staff and management, ensuring the data is maintained to AtomVie standards and regulatory requirements, mentoring and coaching these staff members to understand the importance and implications GDP and data integrity in the laboratory has at AtomVie.
- Ensure compliance with Health and Safety for all policies, procedures and regulations applicable to their work.
What You Bring to the Role
- Working knowledge and thorough understanding of data integrity, Good Documentation Principles (GDP) and concept of 21 CFR Part 11 (and associated regulations)
- Working knowledge of laboratory equipment systems to perform audit trail review of testing
- Familiarity with scientific principles pertaining to analytical records review
- Understanding or principles and requirements for analytical methods qualification, validation and verification
- Aptitude for analytical data analysis and interpretation
- Flexibility in schedule to support a 24/7 operational environment
Requirements
- Post-Secondary Education in Engineering, Chemistry, Microbiology or a related field.
- Minimum 5 years of experience conducting testing or reviewing analytical chemistry data in the pharmaceutical, radiopharmaceutical or biotechnology field.
- Experience working in a GMP environment is required.
- Proficiency in the English language both written and oral, and excellent communication skills; detail oriented.
Compensation
Annual salary starts at $70,000
AtomVie Offers
- Group Health & Dental Benefits (from day 1)
- RRSP Matching Program
- Perkopolis
- Employee Assistance and Wellness Programs
- Transportation/Parking Allowance
AtomVie does not use artificial intelligence or automated decision-making tools in any part of the recruitment, screening, or selection process.
AtomVie is 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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