Drive revalidation activities for process/tool/equipment changes in production Lead process improvement initiatives to enhance productivity, cycle time, and material utilization.
Design experiments and analyze data to optimize process parameters, ensuring consistent product quality.
Develop and implement control plans, process flow diagrams, and PFMEAs to mitigate risks.
Coordinate with vendors and suppliers for equipment selection, procurement, and commissioning.
Develop and maintain detailed documentation, including work instructions, validation protocols (IQ, OQ, PQ), and standard operating procedures (SOPs).
Ensure compliance with electrical and regulatory
Lead initiatives for automation, such as robotic part handling and lights-out manufacturing. Let’s talk about Qualifications and Experience Required
Requirements
Qualifications: Bachelor’s degree in mechanical engineering, Plastics Engineering, Manufacturing Engineering, or a related field. Minimum 3+ years of
experience in Manufacturing Engineering (Ideally with Injection Molding/LSR Manufacturing).
Experience supporting production lines in 24X7 environments. Hands-on
experience with Molding machines and robotic automation Proven track record in leading and supporting engineering projects in highly collaborative environments Strong knowledge of quality systems (ISO 13485, FDA regulations) and validation protocols.
Proficient in CAD software (e.g., SolidWorks) and data analysis tools (e.g., Minitab, JMP). Preferred
Qualifications: Master’s degree in engineering field Familiarity with medical device manufacturing and associated regulatory requirements.
Knowledge of process monitoring systems (e.g., RJG, Kistler).
Six Sigma Green Belt or higher certification.
Strong leadership and project management skills, with a PMP certification preferred.
Ability to manage multiple priorities in a fast-paced, dynamic environment.
Equal Opportunity Employer: ResMed is an equal opportunity employer.
benefits packages, provide flexible work arrangements, cultivate a workforce culture that allows employees to grow personally and professionally, and deliver competitive salaries to our team members.
benefits package: comprehensive medical, vision, dental, and life, AD&D, short-term and long-term disability insurance, sleep care management, Health Savings Account (HSA), Flexible Spending Account (FSA), commuter benefits, 401(k), Employee Stock Purchase Plan (ESPP), Employee Assistance Program (EAP), and tuition assistance.
Employees accrue fifteen days Paid Time Off (PTO) in their first year of employment, receive 11 paid holidays plus 3 floating days and are eligible for 14 weeks of primary caregiver or two weeks of secondary caregiver leave when welcoming new family members.
Individual pay decisions are based on a variety of factors, such as the candidate’s geographic work location, relevant qualifications, work experience, and skills.
At ResMed, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case.
A reasonable estimate of the current base range for this position is: $79,000 to $119,000 Joining us is more than saying “yes” to making the world a healthier place.
Additional details
*Please note the hours for this shift are Monday to Friday 1 PM-10 PM The Manufacturing Engineer (Liquid Silicone Rubber Molding) is a critical role responsible for supporting production lines and manufacturing processes for Liquid Silicone Rubber (LSR) molding operations.
This position involves driving execution of molding technologies, improving efficiency, and ensuring compliance with global quality and regulatory standards in the medical device industry.
The role will also include collaboration with cross-functional teams, vendors, and management to deliver high-quality products while achieving cost and productivity targets. Let’s talk about
Responsibilities Process Optimization: Validate robust manufacturing processes for LSR molding.
Project Management: Serve as the technical lead in root cause investigations and implementing countermeasures.
Provide regular updates to stakeholders, including management, on project status and milestones.
Regulatory Compliance and Documentation: Ensure all processes meet ISO 13485 and FDA regulations for medical device manufacturing.
requirements for North American and European markets.
Collaboration and Cross-Functional Support: Partner with Quality, Manufacturing Engineering, and Production teams to resolve process challenges.
Work with Design Engineering to provide feedback on part designs for manufacturability (DFM).