See yourself at Telix
As a Production Technician reporting to the Production Director, you will play a pivotal role within our brand-new radiopharmaceutical production facilities. Your primary responsibilities will encompass manufacturing of radiopharmaceutical products, from development and validation to clinical and commercial use. Operating in a cutting-edge cleanroom environment, you will adhere to stringent c GMP and radioprotection requirements to ensure the highest quality standards in these crucial medical products.
Key Accountabilities :

• Operates daily in a cleanroom manufacturing environment subject to c GMP and radioprotection requirements.
• Manufactures diagnostic and therapeutic radiopharmaceutical products in accordance with SOPs for development, validation, clinical, and commercial use. This includes aseptic manual and automated radiolabeling and fill-and-finish processing steps.
• Maintains the GMP production area's environment, including equipment and facility cleaning and environmental monitoring.
• Prepares assemblies and solutions according to SOPs and aseptic techniques.
• Performs in-process control testing, such as radioactivity measurement.
• Keeps equipment operating by following operating instructions, troubleshooting breakdowns and calling for repairs.
• Supports projects related to development or optimization of products and procedures and in the qualification of equipment in production areas
• Participates in the writing and revision of QMS documentation related to production (e.g., SOPs, CCRs, deviations, CAPAs, risk assessments, batch records).
• Manages materials and wastes transfer and inventory management in the production area according to SOPs.
• Diligently completes all GMP documentation.
• Participates in the training of new production technicians.
• Effectively communicates with supervisors and colleagues to provide updates on production status and address matters related to safety, quality, and efficiency.
• Uses various computerized systems (e.g. EMS, ERP).
• Supports continuous improvement initiatives.
• Works constructively and flexibly within a team.
• Able to work overtime or out of working hours when required/requested.

Education and Experience

• Bachelor degree in a relevant field, such as chemistry, radiochemistry, pharmacy, biomedical or a related discipline or equivalent relevant experience.
• 3 years of hands-on experience in manufacturing roles in the pharmaceutical or biotech industry.

• Prior experience in the radiopharmaceutical industry is a plus.

• Familiarity with regulations specific to GMP production and handling of radioactive materials.

Key Capabilities

• Adherence to Procedures: Works with precision in strict accordance with established procedures, rules, and regulations.
• Can-Do Attitude: Displays a proactive and hands-on approach, approaching tasks with a positive "can-do" attitude.
• Adaptability: A flexible mindset capable of effectively handling ambiguity and responding energetically and enthusiastically to changes in the work environment.
• Self-Motivated and Team Player: A self-motivated and enthusiastic individual who collaborates well within a team, is eager to learn new skills, and mentors junior staff.
• Proficient in French and intermediate in English.
• Proficient in the use of Microsoft Office applications.