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Boolean Search String:

Standard format for creating search strings:
(“Job Title 1” OR “Job Title 2” OR “Job Title 3”……. OR “Job Title n”) AND (“Main skillset 1” OR “Main
skillset 2” …… OR “Main skillset n”) AND (“Side skillset 1” OR “Side skillset 2” …… OR “Side skillset n”)
AND (Industry/Division)
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Position: Quality Engineer (Medical Devices) with GD&T/Minitab related experience

String 1: High Job Position low Relevant Skill Search String

("Quality Engineer" OR "Validation Engineer" OR "Quality analyst" OR "R&D Engineer") AND ("GD&T"

OR "GD &T" OR "GD& T" OR "GD & T" OR "Minitab" OR "Mini-tab" OR "Mini tab") AND ("Medical
Device" OR "Medical Devices" OR "Med Device" OR "Med Devices" OR "Biomedical" OR "Bio-medical" OR
"Bio medical" OR "Pharma" OR "Pharmaceutical" OR “Healthcare” OR “Health-care” OR “Health care”)

String 2: Low Job Position High Relevant Skill Search String 

("Engineer" OR "Analyst") AND ("Quality" OR "Validation" OR "QA" OR "R&D") AND ("GD&T" OR "GD
&T" OR "GD& T" OR "GD & T") AND ("Minitab" OR "Mini-tab" OR "Mini tab") AND ("Medical Device"
OR "Medical Devices" OR "Med Device" OR "Med Devices" OR "Biomedical" OR "Bio-medical" OR "Bio
medical" OR "Pharma" OR "Pharmaceutical" OR “Healthcare” OR “Health-care” OR “Health care”)
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Position: Technical support Specialist with SAP/ERP/CRM

(“Help Desk” OR “Helpdesk” OR “Service desk” OR “Technical support” OR "Tech Support" OR "Field
Support" OR “Customer Service Support" OR “PC Support” OR "Product support" OR "Client Support" OR
"Phone support" OR “System Support” OR “IT Support” OR “Services Support” OR “Desktop Support” OR
“Global Support”) AND ("ERP" OR "CRM" OR "SAP")
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Here are job position details for your review: 

Job Title: Quality Engineer 3 

Pay Rate: $40 to 48/Hr
Duration: 12 Months
Job Requisition: JP00062540
Location: Flanders, NJ
 

 This position is for Healthcare diagnostics division

This position is for a Senior Quality Engineer with primary responsibility to provide direction in the areas
of Design Controls, Risk Management and Design Transfer to cross-functional teams for new product
development and/or commercialized product. This role will be responsible for reviewing and approving design
changes/change control requests that meet quality requirements. This position requires demonstrated ability to
effectively communicate with peers and management.
Responsibilities:
This position will be responsible for being the Quality Assurance Subject Matter Expert (SME) for Design
Controls, Design Transfer and other change projects, including engineering change and manufacturing process
change projects.
 Serve as reviewer and approver for Design Changes
 Provide guidance and direction in the areas of Design Controls, Risk Management and Design Transfer
to cross functional teams
 Provide guidance on creation of design change implementation plans, including supporting creation of
validation plans, protocols and reports
 Provide guidance and direction for manufacturing changes
Education:
 Bachelor’s degree in science of engineering field of study
Certifications:
 Certified Quality Engineer preferred
Required Skills:
 Demonstrated comprehensive understanding Design Controls, Risk Management and Design Transfer
requirements
 Demonstrated understanding of manufacturing operations and design change/change control
implementation activities
 In-depth knowledge of requirements related to ISO 13485 and FDA QSR
 Experience with reviewing and approving design changes/change control packages
 Strong organizational skills and ability to prioritize
 5-8 years successful experience working in medical device or other regulated industry
 Proficient with Microsoft Office (Excel, PowerPoint, Word, Visio, etc)
 Ability to communicate effectively within a technical environment
 Demonstrated leadership capabilities
 
Direction of Others:
 This is an individual contributor role. Provides specialized direction to professional counterparts on
teams.

Search String:
String 1: High Job Position low Relevant Skill Search String
(“Quality Engineer” OR “Validation Engineer” OR “V&V Engineer”) AND (“risk management” OR “risk
mgmt” OR “risk mgmt.” OR “risk assessment” OR “risk factor” OR “risk elimination” OR “risk mitigation”
OR “risk assessments”) AND (“Design control*” OR “Design history”) AND (“Quality”) AND (Clinical OR
Pharma OR pharmaceutical OR “Biomedical” OR “Bio-medical” OR “Bio medical” OR “Medical device” OR
“Medical devices” OR “Med device” OR “Med devices” OR “Point of care” OR “Biotechnology” OR “Bio-
technology” OR “Bio technology” OR “Biotech” OR “Bio-tech” OR “Bio tech”)

String 2: Low Job Position High Relevant Skill Search String 

(“Engineer”) AND (“Quality”) AND (“risk management” OR “risk mgmt” OR “risk mgmt.” OR “risk
assessment” OR “risk factor” OR “risk elimination” OR “risk mitigation” OR “risk assessments”) AND
(“Design control*” OR “Design history”) AND (Clinical OR Pharma OR pharmaceutical OR “Biomedical” OR
“Bio-medical” OR “Bio medical” OR “Medical device” OR “Medical devices” OR “Med device” OR “Med
devices” OR “Point of care” OR “Biotechnology” OR “Bio-technology” OR “Bio technology” OR “Biotech”
OR “Bio-tech” OR “Bio tech”)
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Here are job position details for your review: 

Job Title: Lab Technician 3 

Pay Rate: $21 to 25/Hr
Duration: 10 Months
Job Requisition: JP00063833
Location: Newark, DE
 

This position is for Healthcare Diagnostics division.

The Lab Technician will be responsible for activities related to manufacturing testing within the Quality
Control Organization. Functions and responsibilities may include and are not limited to: 
 Completes manufacturing related testing/processes on Diagnostic equipment and analyzers such as, DM
Vista, Centaur and Atellica analyzers. 
 Completes manufacturing related testing/processes on analytical instruments such as Titrator, ICP, and
Spectrophotometer and pH meter. 
 Performs the most complex quantitative and qualitative analysis, such as sampling, testing, and
measuring using analytical instruments and diagnostic analyzers. 
 Compiles, analyzes, and interprets test data. 
 Performs complex analysis of data and calculations in excel or LIMS which includes graphs and charts. 
 Enters data into internal software and generates documents as required. 
 Performs periodic inspections of equipment and preventative maintenance work. 
 Maintains instrument logs 
 Ability to follow protocol and schedules 
 Performs troubleshooting on test processes. 
 Interacts with others inside/outside work group: scientists, engineers and management. 
 Potential to work independently on projects which includes defining tasks, setting priorities and
planning materials. 
 Flexible to work overtime and/or irregular work hours as needed. 
 Knowledge of QSR’s and ISO standards. 
 May require participation in new product development, production support and/or reference materials. 
 May provide general guidance to others and train lower level employees. 

Requirements:

Knowledge and skills of a technical or specialty area, with 3-5 years of experience including but not limited to
the following: 
 Understands the quality management system and ensures that their area complies with FDA, QSR, ISO
and IVDD standards. 
 Familiar with GMP, GLP, and GDP processes 
 Mathematical skills: concentration calculations and statistical analysis. 
 Computer skills: customary MS Office programs, SAP, LIMS, and/or Siemens Clinical testing
software. 
 Laboratory skills: operation, maintenance and troubleshooting of analytical instruments
and chemistry assays. 
  Demonstrates ability to work independently, on a team, and be able to multi-task and prioritize daily
work. 
 Strong communication and interpersonal skills. 
 Knowledge of and experience in handling bio-hazard materials. 

Education:
 Bachelor degree in a relevant science (e.g. chemistry, biology, biochemistry), or 2 year degree with
experience in Medical Diagnostics or equivalent) or 5 year degree with experience (e.g. chemistry,
biology, biochemistry, or equivalent). 

Boolean search:
(Chemist OR Biochemist OR “Technician” OR “Tech” OR “Technologist”) AND (“QMS” OR “Quality
system” OR “Quality systems” OR “Quaility management” OR “quality control” OR “quality controls” OR
“QSR” OR “QC”) AND (“Biochemistry” OR Chemistry OR Biology) AND (“Assay” OR “Assays” OR “Wet”
OR “Wetchemistry” OR “Wetlab” OR “Reagent” OR “Reagents” OR “Titration” OR “Titrations” OR “Pipette”
OR “HPLC” OR “gel electrophoresis” OR “Western blot” OR “Western blots” OR “Buffer*” OR
“Spectroscopy”) AND (“Biology” OR “Biochemistry” OR “Chemistry”)