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Job TitleFull Time-Manufacturing Engineer -Colorado Springs, CO-2024
Job Description

This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.

Are you interested in an opportunity with Philips? We welcome individuals who are currently pursuing an undergraduate (BS) degree to participate in opportunities at our site. Through this role you will gain meaningful, hands-on experience working for a HealthTech company.
Job Description
In this role, you have the opportunity to:
become a process and equipment expert responsible for the support of specific product lines and areas as the primary engineering contact. You will design, optimize and develop improvements to processes and equipment to allow products to be manufactured with efficiency and quality while maintaining compliance to ISO and FDA requirements.
You are responsible for:
Our daily work that includes both sustaining and project work we strive to complete the types of projects that remove the need for sustaining work improving safety, quality, output and eliminating scrap.
The team is frequently called to develop solutions to safety or ergonomic concerns, which may involve analyzing work methods, developing fixtures or identifying new ways of doing a task.
Daily sustaining work includes troubleshooting and developing solutions for various chemical and mechanical issues, especially with respect to the following: epoxies, plastic tubing, fiber optics, equipment troubleshooting/repair and packaging. Through the course of these activities, you could encounter the use of analysis tools such as FTIR, DSC, SEM or execute CAD modeling in Solidworks.
Process validation and verification work is frequently required knowledge of Process Validation Plans, IQ, OQ, PQ, Software validation, test method validation, gage R&R, a and a clear understanding of FDAs QSR and cGMP, and a good grounding in statistics would be instrumental to success.
Frequently we must dig deep into problems to fully understand root cause and implement solutions that will prevent reoccurrence. The ME will be expected to organize investigations, pursue a logical course of inquiry, be able to collect and analyze data and see patterns/trends, design controlled experiments and analyze the results of those experiments to make rational conclusions about courses of action.
Together with our production customers, we prioritize the highest value solutions to deliver the quality products our customers need. We care deeply about our customers, both internal and external, and strive to continuously improve our products and processes. We are eager to find teammates who are excited by this atmosphere and the opportunity to make a big difference in the lives of patients!
Contributing to an environment in which all team members are respected regardless of their individual differences and are motivated to improve both their individual and team contributions to achieve desired business results. Training less experienced personnel on established methods and procedures. Facilitating the transfer of technical knowledge, while demonstrating an understanding of those with a diverse background or experience.
Communicating fully with management and others who have a need to know. Being informative and communicating in a way that is timely, prompt, complete, and accurate.
Demonstrate Good Manufacturing Practices (GMP) per regulatory requirements. Working knowledge of quality systems ensuring good documentation practices (GDP) are maintained.
You are a part of
Our Manufacturing Engineering team, a dynamic group of individuals with diverse strengths working together to continuously deliver solutions to meet the needs of our production customers.Successful engineers drive to resolve root cause issues through objective analysis and quick solution delivery. We seek passionate people with a positive mental attitude who can interact with ease within and outside our team to develop and deliver win-win solutions.
To succeed in this role, you should have the following skills and experience
Bachelors of Science degree in an engineering discipline, preferably in Mechanical Engineering but may also be Chemical, Electrical, Biomedical or Materials Engineering degree
Knowledge and experience with Shainin Red-X problem solving, process FMEA, validation/qualification, traceability, and process documentation a plus.
2+ years experience in manufacturing engineering and product/process development, with medical device experience preferred.
Working knowledge of basic PC programs (Word, Excel, Power Point, and basic documentation systems).
Experience in CAD programs required (SolidWorks preferred).
Self-starter, innovative, resourceful, work with minimal direction, and should have excellent skills in problem solving and troubleshooting, oral and written communications, and teaming skills.

Philips Transparency Details

The salary will be between 70k-85k.
The actual base pay offered may vary depending on multiple factors including, job-related knowledge/skills, experience, business needs, geographical location, and internal equity.
Details about our benefits can be found here.
At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case.

Additional Information
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.


Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.