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97 Us Tech Solutions Machining Jobs Hiring Near You

US Tech Solutions

CNC MACHINIST - Direct Hire

Carson City, NV · On-site

$20 - $27.50/hr

Requiring 3-5 years of actual machining or CNC operations. * To perform this job successfully, an ... About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide ...

US Tech Solutions

Solutions Architect

Ottawa, ON · On-site

US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions ...

US Tech Solutions

Solutions Architect

Ottawa, ON · On-site

US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions ...

US Tech Solutions

CNC Programmer #26-15521

Greenville, SC · On-site

$25 - $34/hr

Support machining operations including milling, turning, grinding, and EDM . * Verify and validate ... About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide ...

US Tech Solutions

CNC Programmer #26-15521

Greenville, SC · On-site

$25 - $34/hr

Support machining operations including milling, turning, grinding, and EDM . * Verify and validate ... About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide ...

US Tech Solutions

Quality Technician

Bartlesville, OK · On-site

$15.50 - $20.75/hr

* Maintains and repairs machinery such as engines, motors, pneumatic tools, conveyor systems, and ... US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand ...

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    Infographic showing various Machining job openings at Us Tech Solutions in the United States as of August 2026, with employment types broken down into 7% Full Time, and 93% Contract. Highlights an 79% Physical, 12% Hybrid, and 9% Remote job distribution.

    Specialist Technical Writing #26-19120

    US Tech Solutions

    New Albany, OH • On-site

    Contractor

    Posted 26 days ago

    Job description

    Duration: 24 months Contract
    Description:
    What you will do
    • In this role you will support the manufacturing team and provide technical expertise to regularly draft and revise documents such as Standard Operating Procedures (SOP'S), protocols, technical reports, and training material in a GMP regulated environment that supports the manufacturing process.
    • Develop, review, and update technical content including but not limited to standard operating procedures, work instructions, risk assessments, protocols & reports for manufacturing team.
    • Provide technical and clerical support to the manufacturing team in the preparation of documentation, collation of data and tracking of technical documents.
    • Liaise with manufacturing team and other cross functional departments regarding documentation changes in an effective and timely manner.
    • Collaborate with multiple departments to support new/revise training documentation for manufacturing staff.
    • Support process owners and participate in continuous process improvement and / or troubleshooting projects.
    • Support manufacturing team in reducing document turnaround times.
    • Ensure documentation related actions are completed on time and current schedule is maintained, accurate, and up to date.
    • Develop protocols for Manufacturing to support change controls, deviations & troubleshooting investigations with provision from relevant SMEs.
    • Generate, own, and provide subject matter expertise to Quality System records as minor deviations, CAPA and change control records.
    • Track pending activities required to support change control implementations.
    • Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current operating systems.
    • Share knowledge with members of the manufacturing team.
     
    Preferred Qualifications:
    • Educational Background in Science and/or Engineering.
    • Experience working in GMP pharma and/or biotechnology industry.
    • Experience in a Good Manufacturing Practices (GMP) environment and demonstrated background in technical writing.
    • Experience with device assembly and packaging of final product.
    • Ability to translate highly technical information into easily understandable information for manufacturing operators.
    • Dynamic skills and usage of photographs, drawings, diagrams, animation, and charts that increase users’ understanding.
    • Experience supporting deviations, investigations, CAPA’s and change controls.
    • A fact-based problem solver with strong troubleshooting and problem-solving skills.
    • Pro-active with the ability to prioritize work to meet benchmarks
    • Good documentation and communication
     Basic Qualifications:
    • Doctorate degree OR
    • Master’s degree and 2 years of experience OR
    • Bachelor’s degree and 4 years of experience OR
    • Associates degree and 8 years of experience OR
    • High school diploma / GED and 10 years of experience.
     Top 3 Must Have Skill Sets:
    • GMP background
    • Prior deviation/investigation ownership
    • Excellent written and oral communication
     Preferred:
    • B.S. 2+ YOE would be ideal, previous Veeva experience, and prior deviation and CAPA experience.
     Day to Day Responsibilities:
    • Develop, review, and update technical content including but not limited to standard operating procedures, work instructions, risk assessments, protocols & reports for manufacturing team.
    • Provide technical and clerical support to the manufacturing team in the preparation of documentation, collation of data and tracking of technical documents.
    • Liaise with manufacturing team and other cross functional departments regarding documentation changes in an effective and timely manner.
    • Collaborate with multiple departments to support new/revise training documentation for manufacturing staff.
    • Support process owners and participate in continuous process improvement and / or troubleshooting projects.
    • Support manufacturing team in reducing document turnaround times.
    • Ensure documentation related actions are completed on time and current schedule is maintained, accurate, and up to date.
    • Develop protocols for Manufacturing to support change controls, deviations & troubleshooting investigations with provision from relevant SMEs.
    • Generate, own, and provide subject matter expertise to Quality System records as minor deviations, CAPA and change control records.
    • Track pending activities required to support change control implementations.
    • Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current operating systems.
    • Share knowledge with members of the manufacturing team.
     Note:
    • Fully Onsite - occasional flexibility to WFH (1-2 days per week after 6 months)
    • Standard working hours 8 AM - 5 PM
    • Ideal candidate: B.S. 2+ YOE would be ideal, previous Veeva experience, and prior deviation and CAPA experience.
    About US Tech Solutions:
    US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com.
    US Tech Solutions is an Equal Opportunity Employer.  All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
    AI Statement: By applying, you acknowledge that AI-assisted tools may be used during hiring.
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    About US Tech Solutions

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    US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions.

    Industry

    It services

    Company size

    1,001 - 5,000 Employees

    Headquarters location

    Jersey City, NJ, US

    Year founded

    2000

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