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Our client, a leading Medical Device Manufacturing Company is looking for Quality Engineer 2 and This is for an initial duration of 06 Months Contract – Hunt Valley, MD
 
Job Title: Quality Engineer 2
Job Id: (phone number removed)
Location: Hunt Valley, MD
Duration: 06 Months Contract
Position Type: Hourly Contract Position (W2 only)

Onsite 5 days a week.

Overview :

• Responsible for reviewing and assessing Quality Notifications, Complaints, Deviation/Waivers and other cGMP activities for the assigned product lines in the instrument plant.
• Oversee operations and assure documentation and procedures are followed, updated and maintained as required by internal Quality Policies and related FDA/GMP guidelines.
• Conducts complaint investigations, assists in the investigation of manufacturing issues and provides data and input on technical issues and projects.

Education :

• Bachelor's Degree, BS or BA in related field required with 2 years of experience, or MS with no experience required (project management experience preferred).
• Typical degree in Mechanical or Electrical or Industrial Engineering, Biological Sciences, Chemistry, and/or Computer Science or other related field.

Qualifications :

• 5 years' experience in Quality/Operations.
• Must demonstrate a working understanding of the pertinent Quality Systems Regulations (i.e.: Good Manufacturing Practices, ISO, FDA).
• Proven ability to develop solutions to a variety of problems of moderate scope and complexity, using policies and procedures for guidance.
• Capable of using Microsoft programs and ability to learn other systems.
• Working knowledge of statistical methods as well as statistical application software.
• Effective verbal and written communication skills.
• The ability to work in teams and independently with minimal supervision to obtain results as required.
• Must be self-motivated/directed, organized, detail oriented and have ability to multi-task projects.
• Professional certification is an advantage (i.e. CQA, CQE, SQE, CQM, Six Sigma, etc.).

 
Compensation: The hourly rate for this position is between $58-60 per hour. 
 
Factors which may affect starting pay within this range may include [geography/market, skills, education, experience and other qualifications of the successful candidate].
 
Benefits: Sunrise offers ACA compliant medical coverage/dental insurance/vision insurance to all employees. We also offer Sick time benefits as required per State regulations. 

Qualified candidates please send your word format updated resume at the earliest to Pavan: (url removed) [(phone number removed)].
 
Thank You.

Our client, a leading Medical Device Manufacturing Company is looking for Sr Quality Engineer 2 and This is for an initial duration of 06 Months Contract – Hunt Valley, MD
 
Job Title: Sr Quality Engineer 2
Job Id: (phone number removed)
Location: Hunt Valley, MD
Duration: 06 Months Contract
Position Type: Hourly Contract Position (W2 only)


Onsite 5 days a week.

Overview :

• Responsible for reviewing and assessing Quality Notifications, Complaints, Deviation/Waivers and other cGMP activities for the assigned product lines in the instrument plant.
• Oversee operations and assure documentation and procedures are followed, updated and maintained as required by internal Quality Policies and related FDA/GMP guidelines.
• Conducts complaint investigations, assists in the investigation of manufacturing issues and provides data and input on technical issues and projects.

Education :

• Bachelor's Degree, BS or BA in related field required with 2 years of experience, or MS with no experience required (project management experience preferred).
• Typical degree in Mechanical or Electrical or Industrial Engineering, Biological Sciences, Chemistry, and/or Computer Science or other related field.

Qualifications :

• 5 years' experience in Quality/Operations.
• Must demonstrate a working understanding of the pertinent Quality Systems Regulations (i.e.: Good Manufacturing Practices, ISO, FDA).
• Proven ability to develop solutions to a variety of problems of moderate scope and complexity, using policies and procedures for guidance.
• Capable of using Microsoft programs and ability to learn other systems.
• Working knowledge of statistical methods as well as statistical application software.
• Effective verbal and written communication skills.
• The ability to work in teams and independently with minimal supervision to obtain results as required.
• Must be self-motivated/directed, organized, detail oriented and have ability to multi-task projects.
• Professional certification is an advantage (i.e. CQA, CQE, SQE, CQM, Six Sigma, etc.).

 
Compensation: The hourly rate for this position is between $58-60 per hour. 
 
Factors which may affect starting pay within this range may include [geography/market, skills, education, experience and other qualifications of the successful candidate].
 
Benefits: Sunrise offers ACA compliant medical coverage/dental insurance/vision insurance to all employees. We also offer Sick time benefits as required per State regulations. 

Qualified candidates please send your word format updated resume at the earliest to Pavan: (url removed) [(phone number removed)].
 
Thank You.

Summary:

• Responsibilities may include the following and other duties may be assigned.
• Ensures that suppliers deliver quality parts, materials, and services.
• Qualifies suppliers according to company standards through supplier assessments, process validation reviews, and evaluation of Production Part Approval Process (PPAP) documentation.
• Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur.
• Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met.
• Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation.

Roles & Responsibilities :

• Some individuals may have responsibilities that include Pre-Market Supplier Quality and duties may include:
• Provides Pre-Market Quality Engineering support to New Product Development (NPD) working in partnership with the Component Engineering and Post-Market Supplier Quality Teams, to deliver quality parts, materials, and services, prevent defects, and allow to provide customers with the highest quality and reliable products.
• Provides technical guidance and quality compliance for Supplier Quality engagement throughout the NPD lifecycle on newly qualified parts from NPD and implementing strategies for driving product quality and continuous improvement, ensuring purchased products and components are manufactured and qualified in accordance to applicable industry standards, regulatory requirements, and customer requirements.
• Collaborates with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for new products.
• Define Receiving Inspection requirements as required and associated test method validation for all internal Test Methods.
• Supports supplier change management activities including manufacturing site transfers, process changes, equipment changes, and material changes through risk assessment, supplier audits, PPAP review, and requalification activities

Requirements:

• Bachelor degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. 214.2(h)( 4)(iii)(A) and minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience.

Global high-tech manufacturer producing cutting edge products has an excellent career opportunity for a Quality Engineer on a one year contract basis. Great opportunity to join their awesome team and take full advantage of this rare opportunity!

Job Summary

The Quality Engineer will work on site at its NJ plant for about one year. The QE assists in the implementation and maintenance of all quality system requirements including APQP, Core Tools, customer concerns and customer visits, gauging, process control plans, supplier issues, customer specific requirements.

Main Responsibilities

• Establish and implement process control plans to include capability studies, gage repeatability and reproducibility (Gage R&R) studies.
• Prepares reports by collecting, analyzing, and summarizing data; and making recommendations.
• Development of inspection and work instructions
• Performance process capability studies
• Prepare and submit Production Part Approval Process (PPAP) packages ensuring all elements are met per customer requirements.
• Participate in Advance Product Quality Planning (APQP).
• Participates in and performs Layered Process Audits (LPA) per plan.
• Management of Customer and Internal Complaints, Supplier if needed.

Qualifications

• BS Degree in Engineering
• Professional experience ~5 years
• Automotive experience
• IATF16949 Knowledge
• Manufacturing process experience
• Ability to read and interpret assembly and component drawings and engineering specifications.
• Knowledge in GD&T
• Organization skills with the ability to perform multiple tasks and obtain results working within strict time frames.
• Capacity to work independently from general supervision (must be self-motivated once given direction/guidance)
• Core tools Knowledge
• Problem solving background (8D's Methodology)
• Ability to communicate effectively with all levels of staff and management, both internal and external
• Strong attention to detail
•  

 

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Position Summary

Ensure the accuracy of quality control equipment and systems; effective collection of quality data and carrying out statistical analysis. Support the plant in the identification of quality-related issues. Continuously review product parameters to look for process improvement activities.

Essential Functions/Key Deliverables
" Utilize statistical process control (SPC) techniques as a tool to support process capability and to assist in corrective action activities as appropriate.
" Responsible for the measurement system analysis, which includes the maintenance, scheduling, test planning, calibration and analytical testing, calculations, and reports.
" Develop and implement instructions and methods for inspecting, testing, calibrating, and evaluating products, equipment and processes.
" Ensure Certificate of Acceptance (CoA) reviewed for every produced batch and released in timely manner.
" Ensure certificates for equipment and devices requiring calibration remain current and up to date.
" Assist Quality Manager with quality product development, trial tests, and customer audits.
" Assist with development and assessment of quality training for existing and new employees.
" Assist in root cause analysis for nonconforming products and customer complaints.
" Assist in the execution of a periodic gap analysis between established goals and objectives in terms of product quality.
" Perform special quality tests as required.
" Always use appropriate personal protective equipment (PPE).
" Implement, ensure and monitor all Health & Safety regulations, rules, procedures and policies.
" omply with all environmental requirements as stipulated in ISO and BRCGS standards and guidelines on Health & Safety.
" Monitoring and testing of critical control points (CCPs)
" Member of HARA team.
" Perform any other duty reasonable corresponding with the role.

Knowledge/Skills/Experience
" Engineering degree is a must
" 3 years' experience in a similar position in manufacturing/industrial environment.
" Excellent verbal and written communication skills.
" Troubleshooting and problem-solving skills.
" Previous experience in quality metrics and reporting.
" Excellent time management skills.
" HARA, ISO, and BRCGS knowledge.

JOB TITLE: Advanced Quality Engineer
JOB LOCATION: Canonsburg, PA
WAGE RANGE*: 55-69.85
JOB NUMBER: (phone number removed)

JOB DESCRIPTION: Our client, a large defense contractor, has an immediate opening for an Advanced Quality Engineer to work from their Canonsburg, PA facility. We seek an experienced Advanced Quality Engineer to design, implement and maintain quality assurance protocols and methods for processing materials into finished products. Utilizing your knowledge and experienced you'll have the opportunity to design methods and procedures for inspecting, testing, and evaluating the precision and accuracy of production processes, production equipment and finished products.

QUALIFICATIONS: Bachelor's degree in Engineering, or a related Science or Mathematics field, plus a minimum of 5 years of relevant experience; or Master's degree plus a minimum of 3 years of relevant experience.

CLEARANCE REQUIREMENTS: Department of Defense Secret security clearance obtainable within reasonable time based on requirements. Applicants selected will be subject to a U.S. Government security investigation and must meet eligibility requirements for access to classified information. Due to the nature of work performed within our facilities, U.S. citizenship is required.

What you will be doing:

• Preparation and implementation of Quality Plans based on the internal Quality System and Custom Requirements
• Support tailoring of processes to meet Program requirements
• Monitor build and test activities to ensure compliance to Quality Plans, Customer Requirements, and approved GDMS processes to ensure the proper level of control in place and maintained.
• Ensure proper and effective records of the as-built product configuration
• Monitor and participate in the Deviation and Engineering Change processes to ensure proper change management and transfer to manufacturing is completed in an effective manner
• Monitor nonconformances and apply root cause analysis problem solving to countermeasure known systemic defects
• Perform Program-specific audits and surveillance to evaluate the program's compliance with processes, quality plans, and customer requirements.
• Participate in supplier evaluation and selection processes and monitor supplier performance to identify supplier development opportunities.
• Collect and report quality metrics to identify continuous improvement opportunities
• Lead systemic defect investigations and root cause/corrective action by working cross-functionally
• Implement Quality System policies, procedures, and instructions as required.

What you bring to the table:

• A Bachelor's degree in Engineering, a related specialized area or field is required (or equivalent experience) plus a minimum of 5 years of relevant experience; or Master's degree plus a minimum of 3 years of relevant experience
• Fully proficient knowledge of engineering (i.e., software, electrical, systems, etc.) methodologies, tools, and standards
• Fully proficient knowledge of ISO 9001:2008, CMMI, ISO 14001ASME, ANSI, EIA, etc.
• Fully proficient knowledge of use of relevant inspection/measurement tools and techniques

What sets you apart:

• Experience in defense contracting or similarly regulated industries such as medical device, automotive, or nuclear
• Ability to speak to a specific example of leading a Continuous Improvement initiative with a cross-functional team
• Familiarity with AI tools such as Claude or equivalent platforms
• Background specifically in electro-mechanical or highly technical products (note: candidates with exclusively chemical or laboratory backgrounds will not be considered)
• Identifies opportunities to apply AI for continuous improvement and innovation

What you'll experience:

• Technologies that aren't just top-notch, they're often top-secret
• A team of bold thinkers committed to exploring what's next
• Opportunities to gain new knowledge - as it's discovered

Workplace Options:
This position is fully onsite in Canonsburg, PA.


Equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities

* While an hourly range is posted for this position, an eventual hourly rate is determined by a comprehensive salary analysis which considers multiple factors including but not limited to: job-related knowledge, skills and qualifications, education and experience as compared to others in the organization doing substantially similar work, if applicable, and market and business considerations. Benefits offered include medical, dental and vision benefits; dependent care flexible spending account; 401(k) plan; voluntary life/short term disability/whole life/term life/accident and critical illness coverage; employee assistance program; sick leave in accordance with regulation. Benefits may be subject to generally applicable eligibility, waiting period, contribution, and other requirements and conditions. Benefits offered are in accordance with applicable federal, state, and local laws and subject to change at TCM's discretion.

#Dice

Position Summary

Ensure the accuracy of quality control equipment and systems; effective collection of quality data and carrying out statistical analysis. Support the plant in the identification of quality-related issues. Continuously review product parameters to look for process improvement activities.

Essential Functions/Key Deliverables
" Utilize statistical process control (SPC) techniques as a tool to support process capability and to assist in corrective action activities as appropriate.
" Responsible for the measurement system analysis, which includes the maintenance, scheduling, test planning, calibration and analytical testing, calculations, and reports.
" Develop and implement instructions and methods for inspecting, testing, calibrating, and evaluating products, equipment and processes.
" Ensure Certificate of Acceptance (CoA) reviewed for every produced batch and released in timely manner.
" Ensure certificates for equipment and devices requiring calibration remain current and up to date.
" Assist Quality Manager with quality product development, trial tests, and customer audits.
" Assist with development and assessment of quality training for existing and new employees.
" Assist in root cause analysis for nonconforming products and customer complaints.
" Assist in the execution of a periodic gap analysis between established goals and objectives in terms of product quality.
" Perform special quality tests as required.
" Always use appropriate personal protective equipment (PPE).
" Implement, ensure and monitor all Health & Safety regulations, rules, procedures and policies.
" omply with all environmental requirements as stipulated in ISO and BRCGS standards and guidelines on Health & Safety.
" Monitoring and testing of critical control points (CCPs)
" Member of HARA team.
" Perform any other duty reasonable corresponding with the role.

Knowledge/Skills/Experience
" Engineering degree is a must
" 3 years' experience in a similar position in manufacturing/industrial environment.
" Excellent verbal and written communication skills.
" Troubleshooting and problem-solving skills.
" Previous experience in quality metrics and reporting.
" Excellent time management skills.
" HARA, ISO, and BRCGS knowledge.

Job Description: Support Philips Sleep & Respiratory Care manufacturing transfer activities through supplier qualification, APQP execution, process validation, supplier quality management, and sustaining production support.
Responsibilities:

• Partner with Development, Manufacturing, Procurement, and Suppliers to assess risks and define Critical-to-Quality (CTQ) requirements.
• Lead and execute APQP deliverables for supplier onboarding, product transfer, and change management activities.
• Review and support PFMEA, Control Plans, MSA, SPC, Process Validation, and Line Release activities.
• Support supplier qualification, supplier audits, supplier performance monitoring, and supplier corrective action programs.
• Drive disposition and resolution of supplier quality issues using CAPA, SCAR, Client, 8D, and root cause methodologies.
• Support Design Transfer and Manufacturing Transfer activities from source manufacturing sites to receiving manufacturing facilities.
• Coordinate IQ/OQ/PQ, TMV, validation builds, and process readiness activities.
• Work closely with cross-functional teams to ensure compliance with quality and regulatory requirements throughout the transfer lifecycle.
• Support New Product Introduction (NPI), sustaining engineering, and manufacturing change implementation.

Requirements:

• 5+ years of Supplier Quality Engineering experience in Medical Devices or other regulated industries.
• Hands-on experience with APQP, PPAP/SPPA, PFMEA, Control Plans, MSA, SPC, and Process Validation.
• Strong knowledge of CAPA, SCAR, Client, Root Cause Analysis, and Supplier Quality Systems.
• Experience supporting Manufacturing Transfer, Design Transfer, or NPI programs.
• Working knowledge of ISO 13485 and FDA 21 CFR Part 820 requirements.
• Strong communication and stakeholder management skills.

Preferred Experience:

• Philips / Philips Respironics experience.
• Design Transfer or Manufacturing Transfer Lead experience within respiratory, ventilator, CPAP, or sleep therapy device companies.

Oxford Solutions is seeking a Supplier Quality Engineer for a direct-hire, onsite opportunity. This role will oversee supplier quality across PCBA, electronic assemblies, cable and wire harnesses, machined parts, and fabricated components.

Responsibilities

• Conduct supplier audits and evaluate manufacturing and quality processes
• Serve as the primary supplier quality contact for new product introductions and daily operations
• Partner with Supply Chain, Manufacturing, and Engineering to resolve supplier quality issues
• Review drawings, specifications, inspection requirements, and supplier documentation
• Support supplier qualification, corrective actions, performance improvement, and quality compliance

Qualifications

• Bachelor’s degree in engineering, electronics, or a related field with 3+ years of relevant Supply Chain or Quality experience; An associate degree with 10+ years of directly relevant experience may be considered
• Current supplier auditing experience involving PCBA, machining, and fabrication
• Knowledge of electronic components, cable and wire harness manufacturing, and IPC standards
• Experience with machined and fabricated parts
• Ability to read and interpret engineering drawings and technical specifications
• Strong problem-solving, communication, and cross-functional collaboration skills

Supplier Quality Engineer - Electronics = (phone number removed)

 

Job Description:

• Supplier quality engineers' performance within a fast-paced manufacturing environment.
• The engineers will lead investigations into supplier related non-conformances, drive corrective and preventive actions (CAPAs), and ensure robust execution of first article inspections and part approval processes.
• The position will play a critical role in improving incoming material quality and reducing issues identified during production.
• Candidates will collaborate cross functionally to implement process improvements and enhance supplier accountability. This is a hands on role requiring ownership of quality issues and resolution at scale.

Required Skills:

• Strong experience in supplier quality engineering, including CAPA ownership and root cause analysis.
• Experience managing and closing non-conformance reports (NCRs) in a manufacturing setting.
• Background working with electromechanical components and supplier quality processes.

Nice to Have:

• Experience improving supplier selection and qualification processes.
• Familiarity with incoming inspection control and material quality validation.
• Demonstrated ability to drive process improvements across supplier networks.

Global high-tech manufacturer producing cutting edge products has an excellent career opportunity for a Quality Engineer on a one year contract basis. Great opportunity to join their awesome team and take full advantage of this rare opportunity!

Job Summary

The Quality Engineer will work on site at its NJ plant for about one year. The QE assists in the implementation and maintenance of all quality system requirements including APQP, Core Tools, customer concerns and customer visits, gauging, process control plans, supplier issues, customer specific requirements.

Main Responsibilities

• Establish and implement process control plans to include capability studies, gage repeatability and reproducibility (Gage R&R) studies.
• Prepares reports by collecting, analyzing, and summarizing data; and making recommendations.
• Development of inspection and work instructions
• Performance process capability studies
• Prepare and submit Production Part Approval Process (PPAP) packages ensuring all elements are met per customer requirements.
• Participate in Advance Product Quality Planning (APQP).
• Participates in and performs Layered Process Audits (LPA) per plan.
• Management of Customer and Internal Complaints, Supplier if needed.

Qualifications

• BS Degree in Engineering
• Professional experience ~5 years
• Automotive experience
• IATF16949 Knowledge
• Manufacturing process experience
• Ability to read and interpret assembly and component drawings and engineering specifications.
• Knowledge in GD&T
• Organization skills with the ability to perform multiple tasks and obtain results working within strict time frames.
• Capacity to work independently from general supervision (must be self-motivated once given direction/guidance)
• Core tools Knowledge
• Problem solving background (8D's Methodology)
• Ability to communicate effectively with all levels of staff and management, both internal and external
• Strong attention to detail
•  

 

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.