At a Glance
- Tasks: Develop efficient manufacturing processes for innovative medical devices that change lives.
- Company: Join a global leader in microscopic imaging and medical technology.
- Benefits: Competitive salary, full-time role, and the chance to make a real impact.
- Other info: Collaborative environment with opportunities for professional growth.
- Why this job: Be part of a team transforming patient care with cutting-edge technology.
- Qualifications: Bachelor's degree in engineering and 3 years' experience in manufacturing.
The predicted salary is between 72270 - 88330 $ per year.
Our client is a global leader in microscopic imaging, with patented technologies enabling in vivo imaging of tissues across a wide range of surgical and research applications. Through innovation and collaborations locally and internationally, they are expanding their portfolio and will transform patients’ lives by enabling digital biopsies for cancer screening, diagnosis, and treatment.
The Opportunity
Reporting to the Chief Technology Officer, you will develop safe and efficient manufacturing processes to transfer new medical devices to the production stage:
- Collaborate with design and engineering teams to facilitate the transition from product development to manufacturing, with a focus on DFM.
- Work with stakeholders during product development to transfer designs to safe and efficient manufacturing processes.
- Develop, review, and maintain manufacturing documentation, including work instructions, standard operating procedures (SOPs), and assembly guides.
- Prepare and maintain document packages including BOMs, work instructions and assembly drawings for manufacturing.
- Identify opportunities for process improvements and implement solutions to enhance production efficiency and product quality.
- Support manufacturing by conducting root cause analysis, identifying solutions and introducing process improvements.
- Perform verification and validation of manufacturing processes, including equipment qualification and process validation.
The Requirements
- A bachelor’s degree in engineering (mechanical, mechatronic, manufacturing or similar field).
- At least 3 years’ experience post-graduation in a manufacturing environment, preferably in the medical device industry.
- Strong understanding and/or prior experience in the medical device industry and/or working under ISO 13485:2016, ISO9001 or similar quality management systems.
- Familiarity with design for manufacturability (DFM) principles and experience applying them in product development.
- Excellent written and verbal communication skills with the ability to collaborate effectively with relevant stakeholders.
- Knowledge of electronic circuits and experience in software scripting will be advantageous.
The Offer
The successful candidate will join a team of experts developing cutting edge products to improve clinical decision making and positively impact patients’ lives.
Please email any questions you may have to or call to arrange a time for a confidential discussion with Mark Thomas or Marilyn Jones. To apply, please visit www.mexec.com and click Apply Now to submit your current CV and cover letter.
Production Engineer in Melbourne employer: mexec
At mexec, we pride ourselves on being a leading biomedical research organisation that fosters a culture of innovation and collaboration. Our commitment to excellence is reflected in our investment in advanced technologies and the development of new medicines, providing employees with unique opportunities for professional growth and meaningful contributions to society. Located in Australia, we offer a dynamic work environment where your expertise in business development can thrive, supported by a team dedicated to making a real impact in the field of life sciences.
