דרושים Intern-product Industrialization-latham Ny-summer ב-Philips ב-United States, New York

Are you interested in an co-op opportunity with Philips? We welcome individuals who are currently pursuing an undergraduate (BS) or masters (MS) degree to participate in 6 month co-op opportunities at our site in Latham, NY

• Assist in the design, assembly, and testing of cryogenic systems and superconducting magnets.
• Troubleshoot and resolve mechanical issues related to cryogenic and superconducting systems.
• Collaborate with engineers and scientists to develop and implement design solutions.
• Conduct experiments and tests to evaluate the performance and reliability of prototypes.
• Maintain and calibrate lab equipment to ensure accurate and reliable measurements.

the right fit if:

• Currently pursuing a Bachelor’s degree in Mechanical Engineering Technology or Electrical disciplines.
• Hands-on experience in a laboratory setting, setting up and executing test protocols. Knowledge of safety protocols and standards in a lab environment
• Experience with 3D modeling and other engineering tools. Strong analytical and problem-solving skills

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this

How we work together

This is an office role

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

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The hourly pay range for this position is

Details about our benefits can be found .

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.

Are you interested in an co-op opportunity with Philips? We welcome individuals who are currently pursuing an undergraduate (BS) degree to participate in 6 month co-op opportunities at our site in Latham, NY. Through this role you will gain meaningful, hands-on experience working for a HealthTech company.

• Conduct and perform test activities within a laboratory environment.
• Collaborate with design engineers by receiving instructions and offering constructive feedback.
• Document design inputs and outputs comprehensively.
• Assist and coordinate with vendors for prototype creation.
• Analyze and address issues pertaining to mechanical design, providing effective solutions as needed.

the right fit if:

• Pursuing a Bachelor's degree in one of the following areas of study: Chemistry, Materials Science, Materials Engineering, Chemical Engineering, Bioengineering, design engineering or Electrical Engineering
• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this

How we work together

This is an office role

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

• Learn more about .
• Discover
• Learn more about
• Learn more about

The hourly pay range for this position is $25.00 to $29.00, plus overtime eligible. The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.

Details about our benefits can be found .

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.

Process Quality Engineer (Onsite- Latham, NY)

The Process Quality Engineer at Latham ensures facility and product compliance with ISO 13485 and all relevant regulations, standards, and procedures. They also verify products meet requirements before distribution and lead ongoing quality and process improvements.

Your role:

• The Process Quality Engineer (QE) is a member of the Operations Quality team in Latham and works closely with Area Managers, Team/Group Leads and Manufacturing Engineers (MEs) to optimize production within an area by creating and executing accurate and effective documentation compliant with GDP, documenting and tracking nonconformances, supporting problem-solving and continuous improvement activities, and maintaining documentation verifying effective On the Job Training (OJT) of operators.
• Ensures that executed processes meet the requirements of the site’s QMS, including but not limited to: the creation of Quality Data Sheets (Data Collects), change control, deviations, nonconformances, PFMEAs/control plans, Device History Records (DHRs) and Corrective and Preventive Actions (CAPAs).
• This position reports into the Latham Operations Quality Manager. The employee will work closely with the Operations team responsible for his/her area of oversight, while aligning with the Operations Quality team to ensure compliance, consistency and efficiency throughout the organization.
• This employee will have the opportunity to work closely with other Quality, Manufacturing and Design Engineers on a site that has led innovation in the design of magnets for Magnetic Resonance Imaging (MRI) systems. This position requires the employee to be onsite five days per week.

You're the right fit if:

• You’ve acquired 5+ years of related Quality Engineering experience in the medical device industry. You have strong experience with and understanding of ISO 13485. The ideal candidate will be a change agent and have experience with transformational or change management roles in similar environments previously.
• Your skills include strong process validation experience, PFMEA’s, control plans, and working with statistical analyses tools. Ability to support Nonconformances, CAPA’s, process documentation Design History Review, among other things is required.
• You have a bachelor’s degree or higher in Mechanical Engineering, Electronics Engineering, Science or equivalent. Lean Six Sigma certification preferred but not required.
• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .
• You’re an excellent communicator with an ability to work well cross functionally, and adapt to changing priorities. Requires up to 10% travel as required by business needs.

How we work together

We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.

This is an onsite role, requiring five days per week onsite in Latham.

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

• Learn more about .
• Discover
• Learn more about
• Learn more about

The pay range for this position in Latham, NY is $87,000 to $139,200.

The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.

In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more. Details about our benefits can be found .

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.

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.

Support the Multi-Vendor Services (MVS) Biomedical business as an entry-level Portable Equipment Handler, located onsite at a customer facility in Valhalla, NY. This role will provide administrative support to the onsite biomedical team.Your role:

• Provide an outstanding customer experience, become a viable team member, and quickly get up to speed with technical expertise.

• Identifying and resolving customer issues, providing the customer with the appropriate communication, and involving appropriate site service personnel.

• Responsible for customer relationship management through the effective use of technical knowledge to inspect, ship, and maintain low-risk biomedical equipment at customer sites; generate service revenue; adhere to state and federal regulatory requirements.

• Shift time: Friday - Tuesday: 7 AM - 3 PM, with opportunity for overtime on weekends. Must have the ability to work flexible hours, as needed based on business needs.

• May attend factory training classes and apply lessons learned through on the job training (OJT) and experience.

You're the right fit if:

• Ability to be onsite inValhalla, NY.

• High school graduate or vocational certification in electronics, biomedical equipmentservicing/engineering,or equivalent combination of education and experience in the electronics industry.

• Experience with biomedical equipment or administrative backgrounds in a healthcare/medical setting preferred.

• May require travel to customer sites other than assigned site, zone office, or identified locations for meetings. Occasional overnight stays and travel by air or train may be required for training.

• Ability to understand and utilize technical vocabulary to perform tasks according to either verbal or written instructions.

• Ability to display strong organizational and multi-tasking skills, self-discipline, and autonomy to work independently in a high-pressure environment.

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this.

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.

Product Quality Inspection Technician (2nd Shift)

The In-Process Quality Inspection Technician for our Magnetic Resonance Imaging business is responsible for performing a variety of quality inspection and documentation tasks during the manufacturing process to help reduce defects and increase product quality consistency.

Your role:

• Measure parts and tools accurately using appropriate tools and guidelines during the manufacturing process.
• Conduct quality inspections in SAP to maintain timely and precise inventory tracking.
• Ensure equipment is calibrated and maintained, addressing any issues promptly.
• Document and organize inspection results clearly, adhering to Good Documentation Practices.
• Collaborate with teams and participate in audits, while reporting quality issues and suggesting improvements.

You're the right fit if:

• You’ve acquired 2+ years of experience in quality inspection (preferred) in a manufacturing facility, preferably in a regulated environment (e.g. automotive, aerospace, medical device). Experience with simple measurement and calibration tools required (micrometers, calipers, etc.). Experience with simple measurements, and document measurements required. Experience with inspections and audits in some capacity is required with training available as needed (Welding inspections, pressure testing, hydro testing, HIPOT testing, etc.). Experience inspecting with Coordinate Measuring Machine’s (CMM) preferred but not required. Experience with SAP, Windchill, and MS Office preferred. An ideal candidate will have quality inspection experience or hands on mechanical aptitude skills and be trainable where needed.
• Your skills include ability to read and interpret engineering drawings and proficiency with Geometric Dimensioning & Tolerancing (GD&T). You are knowledgeable about metrology, materials, calibration, auditing and inspection techniques with demonstrated ability to utilize relevant hand tools for these purposes (micrometers, calipers, and other simple hand tools).
• You have a High School Diploma, Vocational Education, or equivalent required, Associate’s degree or higher preferred.
• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .
• You’re an excellent communicator with an ability to work well cross functionally, and comfortability leading without expressed authority. You have strong organizational skills and an ability to prioritize in an environment with rapidly changing priorities.

How we work together

We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.

This is an onsite role on 2nd shift (3:20pm-11:30pm) Mon-Fri.

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

• Learn more about .
• Discover
• Learn more about
• Learn more about

The pay range for this position in Menands, NY is $19.83/hr. to $31.73/hr. There is a 10% pay differential offered for 2nd shift.

The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.

In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more. Details about our benefits can be found .

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.

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.

be provided for this position. For this position, you must reside in
orwithin commuting distance to Latham, NY.

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.

Support the Multi-Vendor Services (MVS) Biomedical business as an entry-level Portable Equipment Handler, located onsite at a customer facility in Valhalla, NY. This role will provide administrative support to the onsite biomedical team.Your role:

• Provide an outstanding customer experience, become a viable team member, and quickly get up to speed with technical expertise.

• Identifying and resolving customer issues, providing the customer with the appropriate communication, and involving appropriate site service personnel.

• Responsible for customer relationship management through the effective use of technical knowledge to inspect, ship, and maintain low-risk biomedical equipment at customer sites; generate service revenue; adhere to state and federal regulatory requirements.

• Shift time: Monday - Friday: 7 AM - 3 PM, with opportunity for overtime on weekends. Must have the ability to work flexible hours, as needed based on business needs.

• May attend factory training classes and apply lessons learned through on the job training (OJT) and experience.

You're the right fit if:

• Ability to be onsite inValhalla, NY.

• High school graduate or vocational certification in electronics, biomedical equipmentservicing/engineering,or equivalent combination of education and experience in the electronics industry.

• Experience with biomedical equipment or administrative backgrounds in a healthcare/medical setting preferred.

• May require travel to customer sites other than assigned site, zone office, or identified locations for meetings. Occasional overnight stays and travel by air or train may be required for training.

• Ability to understand and utilize technical vocabulary to perform tasks according to either verbal or written instructions.

• Ability to display strong organizational and multi-tasking skills, self-discipline, and autonomy to work independently in a high-pressure environment.

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this.

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.

In this role you will be responsible for leading a team of product industrialization engineers to robustly and compliantly satisfy the needs of design transfer to commercial production in an FDA compliant manufacturing environment.

Your role:

• Collaborates with Project Management, R&D, Design Quality, Supplier Quality, Procurement, and Manufacturing Engineering to leverage strengths while developing opportunities over a vast array of manufacturing technologies.

• Interactively shares global best practices as One Philips.

• Participates as local site Management team member.

• Manages a team of 8 – 16 engineering professionals, technicians and interns.

You're the right fit if:

• You’ve acquired 12+ years of successful new product introduction experience in a regulated manufacturing environment.

• Your skills include mastery of APQP, Six Sigma, and Lean applications, structured problem solving and recurrence prevention (CAPA) and team development.

• You have at least a Bachelor of Science degree in engineering or a related field, master’s degree preferred. Formal credentialing in the above skills such as SSBB, PMI PMP, CQE, or similar is highly desirable.

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .

• You’re a success-oriented manager with specific expertise in low volume-high complexity heavy manufacturing fabrication, welding, soldering, electro and mechanical assemblies who can justify business cases and budget control in the ever-challenging FDA environment.

How we work together

This is an onsite role.

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

• Learn more about .

• Discover

• Learn more about

• Learn more about our commitment to

The pay range for this position in New York is $108,850 to $186,600 annually.

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.