Radiopharmaceutical Process Chemist - Hamilton, Canada - AtomVie Global Radiopharma Inc.

AtomVie Global Radiopharma Inc.

Verified Company

Hamilton, Canada

1 week ago

Posted by:

Sophia Lee

beBee Recruiter

Description

AtomVie Global Radiopharma Inc. (AtomVie) is a global leading GMP manufacturer and distributor of clinical and commercial radiopharmaceuticals. We work with our partners to empower the next generation radiotherapeutics for the detection and treatment of cancer and human diseases.

We are a community that challenge ourselves professionally, are proud of what we can accomplish together, and take pride in the impact that we can make with our clients and patients across the globe.

We can't wait for you to begin your career with AtomVie and to help us achieve our vision:
to transform lives by revolutionizing healthcare.

About the Role
This hands-on role will work on site with some flexibility for remote work. Some weeknight and weekend work may be expected according to production schedules.

What You Will Do

Act as a technical expert in GMP process development for AtomVie's clinical and commercial portfolio
Design and conduct radiochemistry experiments for clinical and commercial drug developments
Critically evaluate data, determine appropriate conclusions and a plan of action in collaboration with internal stakeholders to develop phaseappropriate GMP production processes
Provide project data and progress status updates to management and clients
Work with crossfunctional teams on the development of synthesis, purification, formulation and aseptic filling processes, including process transfer, scaleup, validation and launch activities
Support the preparation and review of written procedures, batch records, experimental protocols and reports, specifications and qualification/validation protocols
Prepare technical reports and documents, including SOPs and investigational reports
Emphasize safety in new and existing design and safe practices in all experimental activities for all staff members
Conduct work according to best practices and, where appropriate, regulatory guidance, GMPs, established business processes and protocols, and applicable standard operating procedures

What You Bring to the Role

Take ownership over the projects you lead and feel a sense of accomplishment and pride in the work you produce
Passionate about radiochemistry and the field of radiopharmaceutical science
Planning, designing and executing development activities
Ability to successfully lead multiple projects at a given time while maintaining quality
Strong ability to multitask by prioritizing workload
Excellent communication skills and ability to collaborate well with multiple stakeholders across the entire organization
Ability to work under mínimal supervision and provide key updates to team members and management where required
Attention to detail and well organized
Excellent troubleshooting and analytical skills
Thrive in a team setting and exhibit a high degree of trust and integrity
Maintain the highest standards with respect to safety and radiation protection in all work activities
Flexibility in work schedule to support a 7day work week in support of nightshifttype production environment

Key Qualifications

BSc in chemistry, radiochemistry, biochemistry or equivalent discipline with at least 2 years of relevant laboratory experience and expertise in process development and formulation. MSc or PhD in the abovementioned disciplines is preferred.
Strong knowledge in chemistry, process chemistry, or aseptic manufacturing experience in a pharmaceutical setting is considered an asset.
Knowledge of validation principles, technology transfer of manufacturing processes and GMP concepts is highly desirable.

AtomVie offers