Technical Writing Intern

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 Manufacturing Technical Writing Intern is a 6-month learning-focused internship within the Manufacturing department, designed to provide hands-on exposure to production processes. Working under the guidance of experienced professionals, the intern will assist with documentation, technical writing, and continuous improvement projects while applying Good Manufacturing Practices (GMP) principles. The ideal candidate is detail-oriented, eager to learn, and possesses strong written and verbal communication skills. This internship offers an opportunity to gain practical experience in a regulated manufacturing environment while contributing to the success of the team.

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

• Support continuous improvement initiatives.
• Assist with coordinating project-related activities to ensure tasks are completed on time.
• Complete assigned documentation accurately and promptly, following company standards and Good Manufacturing Practices (GMP).
• Conduct research and gather information to assist in preparing documents and reports.
• Assist in process mapping and help identify opportunities for efficiency improvements.
• Provide support for QMS documentation and help track progress toward departmental goals.
• Participate in change control activities by preparing drafts and supporting follow-up actions under guidance.
• Assist in drafting and revising technical documents such as SOPs, specifications, forms, and templates, ensuring compliance with regulatory guidelines (ICH, USP, etc.).
• Help with quality system documentation including investigation reports and corrective action tracking.
• Support CAPA activities by monitoring progress and assisting with effectiveness checks.
• Assist with documentation for new equipment purchases and installations as needed.
• Collaborate with team members to ensure timely completion of documentation and act as a point of contact for basic inquiries relating to documentation.
• Adhere to GMP regulations by maintaining complete training records pertaining to all aspects of routine operation.
• Perform all tasks in compliance with AtomVie Standard Operating Procedures (SOPs) while maintaining up-to-date knowledge of all manufacturing processes and associated documentation.
• Maintain an updated list of all the current documents used in the manufacturing process at AtomVie.
• Ensure that all work is conducted according to safety policies and regulations.
• Perform other tasks as assigned to support the departments’ objectives and gain exposure to industry practices.

Experience Necessary

Compensation

Hourly Rate : $22.00

AtomVie Offers

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.