Burlington offers 821 current healthcare opportunities for professionals at all experience levels. Whether you're seeking entry-level positions, mid-career development, or senior leadership roles, the healthcare sector in Burlington provides diverse career growth paths.
Why Choose Burlington for Healthcare?
✓Growing market: 821 active positions in the healthcare sector
✓Flexible options: Available opportunities for full-time, part-time, contract, and remote work
✓Career development: Opportunities for advancement and professional growth
Nearby Cities with Healthcare Opportunities
Consider expanding your search to nearby cities: Canada (8K listings), Toronto (8K listings), Calgary (3K listings), Vancouver (3K listings) and Edmonton (2K listings).
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Healthcare Jobs in Burlington
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Yes! Nearby cities with healthcare opportunities include Canada (8K listings), Toronto (8K listings), Calgary (3K listings), Vancouver (3K listings) and Edmonton (2K listings).
Updated June 2026 • Active Listings
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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 Radiopharmaceutical Scientist serves as a technical subject matter expert in radiochemistry, automated synthesis, purification, and process development. This is an advanced-level individual contributor role responsible for driving product development activities from early-stage research through readiness for routine GMP manufacturing. The Scientist applies deep expertise in process design, optimization, and characterization to ensure development programs are executed efficiently, delivered on time and within scope, and aligned with regulatory and GMP requirements.
Working collaboratively with Process Development, Manufacturing, Quality, and Regulatory teams, the Scientist supports process scale-up, technology transfer, and commercialization while maintaining accountability for Product Development deliverables and scientific integrity. The role contributes to resolving development and manufacturing challenges through data-driven recommendations and technical guidance, particularly during tech transfer and early-stage GMP execution, without direct oversight of Manufacturing activities.
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
- Design and execute radiopharmaceutical process development, including radiolabeling, conjugation, purification, and formulation for therapeutic and diagnostic programs.
- Design and implement phase-appropriate process development strategies, including DOE, process optimization, and process characterization.
- Develop robust and scalable processes suitable for clinical and commercial GMP manufacturing.
- Identify and define Critical Process Parameters (CPPs), Critical Quality Attributes (CQAs), and control strategies.
- Interpret and critically evaluate experimental data to ensure scientific integrity, troubleshoot development challenges, and define next-stage development strategies.
- Provide hands-on technical support and guidance to ensure successful execution of development activities.
- Serve as a subject matter expert in radiochemistry and process chemistry.
- Evaluate and introduce current technologies and process improvements to enhance development efficiency and robustness.
- Support planning and execution of development programs to meet project timelines, scope, and budget expectations.
- Contribute to process scale-up, technology transfer, validation, and launch activities.
- Ensure development activities are executed in accordance with defined process specifications and expected outcomes.
- Maintain working knowledge of regulatory guidance, pharmacopeial standards, internal procedures, and SOPs.
- Author, review, and maintain technical documentation, including process development reports, validation protocols, and SOPs, in accordance with Good Documentation Practices.
- Support preparation of CMC sections for regulatory submissions (IND, CTA, NDA, etc.).
- Support non-conformances (NCR's), investigations, CAPAs, and change controls related to development activities.
- Promote quality-by-design (QbD) principles and a “right-first-time” culture.
- Act as a technical interface for internal teams and clients during development stages.
What You Bring to the Role
- 5+ years of relevant industry experience.
- Hands-on experience in radiochemistry, radiopharmaceutical development, or process chemistry.
- Experience working in or supporting GMP environments.
- Experience with radiolabeling and isotope handling (therapeutic and/or diagnostic isotopes).
- Familiarity with CMC development and regulatory documentation is strongly preferred.
- Experience with analytical characterization techniques relevant to radiopharmaceuticals.
Requirements
• PhD in Chemistry (preferred), Biochemistry, Chemical Engineering or related field.
Compensation:
Annual salary starts at $95k.
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 serv
