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Added 27 mins ago
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Quality Assurance Associate- Batch Release
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The QA Associate for Batch Release is responsible for final disposition of incoming materials and final radiopharmaceutical drug product batches. This role ensures that all batches meet…
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Quality Assurance Associate - Batch Release
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Full-time
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AtomVie Global Radiopharma

Quality Assurance Associate- Batch Release

Hamilton, ON, Canada

Pay: Up to $65,000 CAD / year
Job type: Full-time
Posting language: English
Posted: Sep 25, 2026

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Original job description

AtomVie Global Radiopharma Inc.is a global leading GMP manufacturer and distributor 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 Associate for Batch Release is responsible for final disposition of incoming materials and final radiopharmaceutical drug product batches. This role ensures that all batches meet specifications, are manufactured/packaged in accordance with validated processes and are compliant with cGMP requirements and regulatory requirements.

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

Determine final disposition of batches by reviewing all required documentation, including but not limited to batch records and change controls, and determining the status of deviations
Complete media fill reviews, reporting any issues
Participate in the creation and revision of standard operating procedures, and specifications
Review Certificates of Analysis, material management or other similar documentation for internal and external customers
Release incoming materials (e.g. activity, raw materials, components etc.) using the ERP system
Act as liaison with clients for batch related issues.
Assist in drafting and finalizing Annual Product Quality Reviews
Provide support for the launch of new products
Provide support for to Management by gathering and analyzing data
Recommend, support and drive cross-functional and interdepartmental continuous improvement efforts
Provide support to internal and external audits by AtomVie and participate in regulatory inspections of AtomVie facilities, as needed
Plan, implement, and successfully complete assigned tasks in a timely fashion ensuring consistent high quality.
Support and implement corrective actions (CAPA) where required
Adhere to GMP regulations by maintaining complete records and ensuring compliance with Health Canada, FDA, and EMA requirements for sterile pharmaceuticals.
Ensure compliance with Health and Safety for all policies, procedures and regulations applicable to their work.
Complete other duties as assigned

What You Bring To The Role

Proficiency in the English language both written and oral and excellent communication skills; detail-oriented
Ability to work independently and possess excellent organizational skills.
A collaborative mindset, with the ability to work cross-functionally with various teams.
High attention to detail and the ability to maintain accuracy in reviewing batch records, documentation, and regulatory compliance.

Requirements

A B.Sc or M.Sc in the life sciences with 3-5 years of experience in a GMP or equivalent regulated environment is preferred.
In-depth knowledge of key regulations and guidance documents, pertinent to Product Development and Quality including Health Canada, FDA, EU GMP, ICH and ISO, with specific knowledge of the regulations as they pertain to sterile products
Flexibility to support the operational needs of a 24/7 production environment. The work schedule for this position will include shifts scheduled from Sunday through to Saturday

Compensation

Annual salary starts at $65,000. 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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More about this job

Responsibilities

The QA Associate is responsible for the final disposition of incoming materials and radiopharmaceutical drug product batches to ensure compliance with cGMP and regulatory standards. They will also support internal and external audits, manage CAPA processes, and assist in the creation of standard operating procedures.

Requirements

Candidates should hold a B.Sc or M.Sc in life sciences with 3-5 years of experience in a GMP or regulated environment. In-depth knowledge of Health Canada, FDA, EU GMP, ICH, and ISO regulations regarding sterile products is required.

Skills

Quality Assurance
Batch Release
GMP Compliance
Regulatory Compliance
Documentation Review
Deviation Management
Media Fill Review
SOP Creation
ERP System
CAPA
Data Analysis
Communication Skills
Organizational Skills
Attention To Detail
Sterile Pharmaceuticals

Benefits

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

Visa sponsorship

Not detected in the job text

Keywords

Quality Assurance
Batch Release
GMP
Radiopharmaceuticals
Health Canada
FDA
EU GMP
ICH
ISO
Sterile Pharmaceuticals
CAPA
SOP
ERP
Documentation
Compliance
Regulatory Affairs
Life Sciences
Continuous Improvement
Audits
Annual Product Quality Reviews

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