Mechanical Design Engineer II at Telix Pharmaceuticals (Americas)

Burnaby, British Columbia, Canada -

Full Time

Start Date

Immediate

Expiry Date

20 May, 26

Salary

0.0

Posted On

19 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Mechanical Design, 3D CAD, Solidworks, 3D Printing, Rapid Prototyping, cGMP, ISO Standards, Nuclear Safety, Design Reviews, FMEAs, Root Cause Analysis, ECO Implementation, Technical Documentation, Product Lifecycle Management, Troubleshooting

Industry

Pharmaceutical Manufacturing

Description

Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases. See Yourself at Telix The Mechanical Design Engineer II supports the design, maintenance, and continuous improvement of ARTMS products, with a primary focus on existing systems including solid target stations, transfer systems, and equipment used in cyclotron‑based isotope manufacturing and processing. This role contributes to mechanical design activities, design updates, and manufacturing support under the guidance of senior engineering staff. Key Accountabilities: Mechanical Design & Product Support Contribute to mechanical design and product development activities for existing products, from concept modifications through implementation. Prepare and update engineering drawings, specifications, and technical documentation. Participate in design reviews and assist with dFMEAs/pFMEAs and other risk management activities. Support testing and validation activities to verify design performance and compliance with requirements. Engineering Changes & Continuous Improvement Implement engineering change orders (ECOs) related to reliability, manufacturability, or cost improvements. Assist in evaluating and updating components, assemblies, and documentation as part of ongoing product lifecycle management. Cross‑Functional Collaboration Work closely with Chemistry, Manufacturing, and Quality teams to ensure material considerations, production needs, and quality requirements are incorporated into mechanical designs. Support production by troubleshooting mechanical issues and recommending process or design improvements. Participate in investigations of nonconformances and contribute to root cause analysis and corrective/preventive actions. Compliance & Safety Follow safe work practices and maintain a clean, organized working environment. Adhere to applicable regulatory requirements including cGMP, ISO standards, nuclear safety, and transportation/dangerous goods regulations. Support development and continuous improvement of QC, QA, and QMS processes, including participation in internal compliance audits. Other Requirements May require training as a Nuclear Energy Worker (NEW). Performs other engineering tasks as assigned to support team and project objectives. Education and Experience: Bachelor’s degree in mechanical engineering or related field required 5 years’ experience (Bachelors degree), 3+ years’ experience (Masters degree), 2+ years’ experience (PhD) required Ability to communicate clearly and professionally both in writing and verbally Strong mechanical design skills using 3D CAD, Solidworks preferred Attention to detail, self-motivated, and able to achieve assigned goals and objectives Experience with 3D printing/ rapid prototyping Occasional extended hours or shift work may be required. Some travel, including international travel, may also be necessary (up to 10%) Knowledge and experience working within GMP, compliance regulations and/or ISO9001 standards EIT registration with EGBC (PEng preferred) Key Capabilities: Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development. Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics. VIEW OUR PRIVACY POLICY HERE

Responsibilities

The Mechanical Design Engineer II supports the design, maintenance, and continuous improvement of ARTMS products, focusing on systems for cyclotron-based isotope manufacturing, including preparing engineering drawings and participating in design reviews. This role also involves implementing engineering changes, troubleshooting mechanical issues in production, and ensuring designs comply with regulatory requirements like cGMP and ISO standards.