ResMed

Manufacturing Engineer (2nd Shift)

ResMed$79K — $119K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in mechanical engineering, Plastics Engineering, Manufacturing Engineering, or a related field.
  • Minimum 3+ years of experience in Manufacturing Engineering, ideally focused on LSR or injection molding.
  • Hands-on experience with molding machines and robotic automation.
  • Proven track record of leading engineering projects in collaborative environments.
  • Strong knowledge of quality systems (ISO 13485, FDA regulations) and validation protocols.
  • Proficient in CAD software (SolidWorks) and data analysis tools (Minitab, JMP).

Responsibilities

  • Validate and optimize manufacturing processes for LSR molding.
  • Lead process improvement initiatives to enhance productivity and material utilization.
  • Design experiments to analyze and optimize process parameters for product quality.
  • Serve as technical lead in root cause investigations and implement countermeasures.
  • Coordinate equipment selection and procurement with vendors and suppliers.
  • Ensure compliance with ISO 13485 and FDA regulations for medical device manufacturing.
  • Collaborate with cross-functional teams to resolve process challenges and improve manufacturability.

Benefits

  • Opportunity to work on transformative manufacturing technologies.
  • Collaborative and innovative work environment.
  • Professional development opportunities.
  • A chance to contribute to products that improve lives globally.
  • Commitment to responding to every applicant.
Full Job Description
*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.
  • 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.


  • Project Management:
  • Serve as the technical lead in root cause investigations and implementing countermeasures.
  • Coordinate with vendors and suppliers for equipment selection, procurement, and commissioning.
  • 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.
  • Develop and maintain detailed documentation, including work instructions, validation protocols (IQ, OQ, PQ), and standard operating procedures (SOPs).
  • Ensure compliance with electrical and regulatory 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).


  • Innovation and Continuous Improvement:
  • Research and integrate emerging technologies in LSR molding to improve efficiency and reduce waste.
  • Lead initiatives for automation, such as robotic part handling and lights-out manufacturing.


Let's talk about Qualifications and Experience

Required 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.


Core Competencies:
  • Analytical problem-solving and decision-making skills.
  • Excellent communication and interpersonal abilities.
  • Detail-oriented with a strong commitment to quality and compliance.
  • Ability to manage multiple priorities in a fast-paced, dynamic environment.
  • Team player with a proactive approach to innovation and continuous improvement.


At ResMed you will have the opportunity to work on transformative manufacturing technologies in a collaborative and innovative environment. We offer competitive benefits, professional development opportunities, and a chance to contribute to products that improve lives globally.

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. It's discovering a career that's challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates. If this sounds like the workplace for you, apply now! We commit to respond to every applicant.

About ResMed

ResMed is a global leader in the development, manufacturing, and marketing of medical devices and software solutions for the treatment of sleep apnea, chronic obstructive pulmonary disease (COPD), and other respiratory disorders. The company's products include continuous positive airway pressure (CPAP) machines, masks, and accessories, as well as ventilators and other respiratory care devices. ResMed serves patients and healthcare providers in more than 140 countries worldwide. The company was founded in 1989 and is headquartered in San Diego, California.
Learn more about ResMed
Size
7,970 employees
Market Cap
$30.4 billion
Industry
Net Income
$698.8 million
Founded
1989
5 Year Trend
+11.6%
Revenue
$3 billion
NASDAQ

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