Radiopharmaceutical Process Chemist
7 months ago
**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 phase-appropriate GMP production processes
- Provide project data and progress status updates to management and clients
- Work with cross-functional teams on the development of synthesis, purification, formulation and aseptic filling processes, including process transfer, scale-up, 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 7-day work week in support of nightshift-type 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**
- Group Health & Dental Benefits (starts from Day 1)
- RRSP Matching Program
- Perkopolis
- Employee Assistance and Wellness Program
- Parking Allowance
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.
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