Highlights
Perform moderately complex assignments, applying established methods to recurring situations;escalate more complex issues to senior quality personnel. Support Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory initiatives.
Numbers & Facts
| Location | Irving, TX |
| Industry | Staffing/Employment Agencies |
| Salary | $20 |
| Company Size | 2,000 to 2,499 employees |
| Year Founded | 2000 |
| Website | http://www.lancesoft.com/ |
Description
Description:
Duties & Key Responsibilities
Support manufacturing and testing operations in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) for receiving and inspection.
Perform job duties in accordance with Client Global and Technical Standards and Quality System (QS) requirements.
Complete Tier 1 inspections per inspection plans and drawings to support production schedules.
o Use hand tools (calipers, gauges, rulers) and perform visual inspections on inbound materials for medical device assembly.
o May operate more advanced measuring instruments as needed.
Perform visual and dimensional inspections of cable harness assemblies and printed circuit board assemblies.
Maintain accurate inspection records, documentation, and filing systems to meet GMP and quality compliance.
Accept or reject supplier lots based on inspection results.
Document any non conformances related to specifications, procedures, or standards, including completing required paperwork and system transactions.
Initiate discrepant material reports and participate in data collection, analysis, and trending.
Recommend improvements to policies, processes, and procedures.
Perform moderately complex assignments, applying established methods to recurring situations;escalate more complex issues to senior quality personnel.
Support Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory initiatives.
Ensure adherence to all FDA, ISO, environmental, health, and safety requirements.
Key Skills
Ability to perform accurate visual and dimensional inspections.
Knowledge of GMP, GLP, and quality system regulations.
Strong documentation and record keeping skills.
Ability to analyze inspection data and identify trends.
Attention to detail and accuracy.
Ability to follow standards, procedures, and regulatory guidelines.
Basic problem solving and initiative to complete tasks independently.
Required Experience
0 2 years performing incoming dimensional inspections.
Experience with hand measurement tools such as calipers, gauges, and rulers.
Work experience supporting manufacturing or quality environments preferred.
Intern will be considered
Preferred Experience (Nice to Have)
Bachelor s degree or technical diploma (not required but preferred if no prior inspection experience).
Familiarity with medical device manufacturing or regulated environments.
Experience reviewing engineering drawings, specifications, and inspection plans (required)
Education
High School Diploma or GED required.
Duties & Key Responsibilities
Support manufacturing and testing operations in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) for receiving and inspection.
Perform job duties in accordance with Client Global and Technical Standards and Quality System (QS) requirements.
Complete Tier 1 inspections per inspection plans and drawings to support production schedules.
o Use hand tools (calipers, gauges, rulers) and perform visual inspections on inbound materials for medical device assembly.
o May operate more advanced measuring instruments as needed.
Perform visual and dimensional inspections of cable harness assemblies and printed circuit board assemblies.
Maintain accurate inspection records, documentation, and filing systems to meet GMP and quality compliance.
Accept or reject supplier lots based on inspection results.
Document any non conformances related to specifications, procedures, or standards, including completing required paperwork and system transactions.
Initiate discrepant material reports and participate in data collection, analysis, and trending.
Recommend improvements to policies, processes, and procedures.
Perform moderately complex assignments, applying established methods to recurring situations;escalate more complex issues to senior quality personnel.
Support Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory initiatives.
Ensure adherence to all FDA, ISO, environmental, health, and safety requirements.
Key Skills
Ability to perform accurate visual and dimensional inspections.
Knowledge of GMP, GLP, and quality system regulations.
Strong documentation and record keeping skills.
Ability to analyze inspection data and identify trends.
Attention to detail and accuracy.
Ability to follow standards, procedures, and regulatory guidelines.
Basic problem solving and initiative to complete tasks independently.
Required Experience
0 2 years performing incoming dimensional inspections.
Experience with hand measurement tools such as calipers, gauges, and rulers.
Work experience supporting manufacturing or quality environments preferred.
Intern will be considered
Preferred Experience (Nice to Have)
Bachelor s degree or technical diploma (not required but preferred if no prior inspection experience).
Familiarity with medical device manufacturing or regulated environments.
Experience reviewing engineering drawings, specifications, and inspection plans (required)
Education
High School Diploma or GED required.
About Company
We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc).
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.