★ Service Disabled ★
Veteran Owned business
Veteran Owned business
★ Service Disabled Veteran Owned business ★
We believe in the power of people. Our mission is to match top talent with leading companies across the country. Whether you’re looking for temporary work, contract assignments, or a long-term career move, we take the time to understand your goals and connect you with the right opportunity. That’s why 97% of our employees say Amerit is the best company they’ve ever worked for.
Pre and post tax contributions to help you retire strong.
Fast, secure, and flexible payroll.
Earn up to $500 for referring qualified candidates.
Savings on entertainment, travel, and more.
Affordable group coverage for full-time employees.
Confidential help for personal and family challenges.
Pre-tax savings on transit and parking.
Coverage to keep your pets healthy and your mind at ease.
We don’t just place you in a role; we support you throughout your career journey. Every Amerit employee has access to a Single Point of Contact (SPOC) who serves as your advocate, ensuring your questions are answered and your needs are met. We work with professionals at all levels, from recent graduates to executives, and connect candidates with industries such as:
Amerit partners with Fortune 500 companies and leading organizations to connect you with opportunities that fit your skills and goals. From full-time placements to flexible contracts and executive roles, we help you take the next step in your career.
Provide strong technical expertise and engineering support for the design and development of both new and existing products. This includes addressing product quality, manufacturing efficiency, supply continuity, and cost optimization
Pay: $50/hr. – $54/hr.
Location: Franklin Lakes, NJ 07417 (On-site)
Our client, a Global Fortune 50 organization and one of the world’s largest distributors of healthcare systems, medical supplies & pharmaceutical products, seeks an accomplished Sr Technology Sourcing Procurement Manager.
Pay: $55/hr. – $59/hr.
Location: Richmond VA, Atlanta GA or Dallas TX (Remote)
Our client, one of the largest Energy companies in the US, providing a wide range of energy-related products and services to its customers, seeks an accomplished Project Administrative Coordinator.
Pay: $25/hr. – $30/hr.
Location: Pearl River, NY 10965 (Hybrid)
Our client, a Global Fortune 50 organization and one of world’s largest distributors of Health care systems, medical supplies & Pharmaceutical products, seeks an accomplished “Pharmacist”.
Pay: $55/hr. – $60/hr.
Location: Fort Worth, TX 76177 (On-site)
Our client, a Medical Center facility under the aegis of a California Public Ivy university and one of largest health delivery systems in California, seeks accomplished Animal Technician.
Pay: $25/hr. – $27/hr.
Location: San Francisco, CA 94158 (On-site)
The Regulatory Affairs Specialist will be responsible for planning, coordinating, and implementing regulatory strategies for medical device products that require government approval. This role involves working closely with a global team (including Asia, Mexico, Korea, and Taiwan) and may require late afternoon calls. The position will start on-site before transitioning to a hybrid schedule.
Pay: $60/hr. – $70/hr.
Location: Irvine, CA, 92603 (On-site)
Provide strong technical expertise and engineering support for the design and development of both new and existing products. This includes addressing product quality, manufacturing efficiency, supply continuity, and cost optimization
Pay: $50/hr. – $54/hr.
Location: Franklin Lakes, NJ 07417 (On-site)
Duration: 12-month contract with possible extension
Relocation Assistance: Not available
Eligibility: Must be authorized to work in the U.S. without requiring sponsorship
The Product Development Engineer II provides technical expertise and engineering support for the design and development of both new and existing products. This role focuses on product quality, manufacturing efficiency, supply continuity, and cost optimization while ensuring compliance with regulatory standards.
Support design and development activities across new and legacy products.
Resolve issues related to product quality, manufacturing efficiency, and cost effectiveness.
Collaborate on cross-functional teams, providing timely and accurate technical input.
Propose innovative product concepts and enhancements.
Gather customer insights through literature reviews, interviews, observations, and competitive analysis.
Translate customer and business requirements into engineering specifications and designs.
Develop robust, manufacturable solutions using sound engineering principles.
Design and execute validation test methods, including test setup, measurement systems analysis, and data analysis.
Prepare detailed technical documentation to support design verification, changes, and regulatory requirements.
Bachelor’s degree in Engineering (Mechanical or Biomedical Engineering preferred).
2–4 years of engineering experience, ideally in the medical device industry.
Experience with Design Control, Risk Management, Quality, and Regulatory requirements.
Injection molding (plastics) knowledge strongly preferred.
Proficiency in statistical tools and computer-based analysis.
Strong problem-solving skills with ability to apply engineering fundamentals to practical challenges.
Our client, a Global Fortune 50 organization and one of the world’s largest distributors of healthcare systems, medical supplies & pharmaceutical products, seeks an accomplished Sr Technology Sourcing Procurement Manager.
Pay: $55/hr. – $59/hr.
Location: Richmond VA, Atlanta GA or Dallas TX (Remote)
Duration: 8-month contract (possibility of extension or conversion to FTE)
Work Type: Remote (with occasional travel for team meetings or supplier engagement)
Eligibility: Must be authorized to work in the U.S. without requiring sponsorship
We are seeking a high-performing and detail-oriented Senior Manager to support contract separation and sourcing efforts as we establish a new, independent business unit. This role will work closely with the Interim Strategic Sourcing Lead to manage supplier transitions, execute technology sourcing initiatives, and build a future-state indirect procurement model. The ideal candidate brings strong hands-on sourcing expertise—particularly in technology—and proven experience navigating contract disentanglement within complex enterprise agreements.
End Goal: Ensure the new standalone business is fully operational by May 1, 2026, with its own indirect procurement model and supplier agreements, while reducing value leakage, minimizing rework, and supporting team balance.
Our client, one of the largest Energy companies in the US providing a wide range of Energy-related products and services to its customers, seeks an accomplished Project Administrative Coordinator.
Pay: $25/hr. – $30/hr.
Location: Pearl River, NY 10965 (Hybrid)
Duration: 26-week contract (possibility of extension)
Work Hours: Monday–Friday, 6:30am–3:00pm or 7:00am–3:30pm (schedule determined by hiring manager)
Work Type: Onsite
Eligibility: Must be authorized to work in the U.S. without requiring sponsorship
The Animal Care Technician is responsible for animal husbandry, sanitation, health monitoring, and record-keeping in a biomedical research environment. This role ensures the highest standards of care and compliance with regulatory requirements.
Our client, a Global Fortune 50 organization and one of world’s largest distributors of Health care systems, medical supplies & Pharmaceutical products, seeks an accomplished “Pharmacist”.
Pay: $55/hr. – $60/hr.
Location: Fort Worth, TX 76177 (On-site)
Duration: 12-month contract with possible extension
Relocation Assistance: Not available
Eligibility: Must be authorized to work in the U.S. without requiring sponsorship
The Product Development Engineer II provides technical expertise and engineering support for the design and development of both new and existing products. This role focuses on product quality, manufacturing efficiency, supply continuity, and cost optimization while ensuring compliance with regulatory standards.
Support design and development activities across new and legacy products.
Resolve issues related to product quality, manufacturing efficiency, and cost effectiveness.
Collaborate on cross-functional teams, providing timely and accurate technical input.
Propose innovative product concepts and enhancements.
Gather customer insights through literature reviews, interviews, observations, and competitive analysis.
Translate customer and business requirements into engineering specifications and designs.
Develop robust, manufacturable solutions using sound engineering principles.
Design and execute validation test methods, including test setup, measurement systems analysis, and data analysis.
Prepare detailed technical documentation to support design verification, changes, and regulatory requirements.
Bachelor’s degree in Engineering (Mechanical or Biomedical Engineering preferred).
2–4 years of engineering experience, ideally in the medical device industry.
Experience with Design Control, Risk Management, Quality, and Regulatory requirements.
Injection molding (plastics) knowledge strongly preferred.
Proficiency in statistical tools and computer-based analysis.
Strong problem-solving skills with ability to apply engineering fundamentals to practical challenges.
Our client, a Medical Center facility under the aegis of a California Public Ivy university and one of largest health delivery systems in California, seeks accomplished Animal Technician.
Pay: $25/hr. – $27/hr.
Location: San Francisco, CA 94158 (On-site)
Duration: 26-week contract (possibility of extension)
Work Hours: Monday–Friday, 6:30am–3:00pm or 7:00am–3:30pm (schedule determined by hiring manager)
Work Type: Onsite
Eligibility: Must be authorized to work in the U.S. without requiring sponsorship
The Animal Care Technician is responsible for animal husbandry, sanitation, health monitoring, and record-keeping in a biomedical research environment. This role ensures the highest standards of care and compliance with regulatory requirements.
The Regulatory Affairs Specialist will be responsible for planning, coordinating, and implementing regulatory strategies for medical device products that require government approval. This role involves working closely with a global team (including Asia, Mexico, Korea, and Taiwan) and may require late afternoon calls. The position will start on-site before transitioning to a hybrid schedule.
Pay: $60/hr. – $70/hr.
Location: Irvine, CA, 92603 (On-site)
Duration: 18-month contract
Relocation/Interview Expenses: Not available
Work Arrangement: Onsite initially (5 days/week), transitioning to hybrid schedule
Eligibility: Must be authorized to work in the U.S. without requiring sponsorship
The Regulatory Affairs Specialist is responsible for planning, coordinating, and executing regulatory strategies for medical device products requiring government approval. This role involves collaborating with a global team across Asia, Mexico, Korea, and Taiwan and may require late-afternoon calls. The position begins onsite and will transition to a hybrid schedule.
Develop and implement regulatory strategies for products requiring approval or clearance.
Apply regulatory knowledge to support product submissions and compliance activities.
Prepare, review, and refine submission materials to meet regulatory standards.
Translate complex technical data into clear, reviewer-ready documentation.
Liaise with regulatory agencies to facilitate timely approvals.
Contribute to the strategic planning of regulatory pathways for new and existing products.
Retrieve and manage reports, protocols, and license transfers (over 6,000 documents) within Windchill.
Provide guidance and serve as a resource for less experienced colleagues.
Work independently with minimal supervision, effectively prioritizing tasks.
Education: Bachelor’s degree in Engineering (required).
1–2 years of regulatory affairs experience (medical device industry preferred).
Experience preparing regulatory submissions and ensuring compliance with requirements.
Familiarity with Windchill document management system (preferred).
Strong understanding of healthcare regulations and industry practices.
Ability to manage both routine and complex regulatory issues.
Excellent organizational, documentation, and communication skills.
Skilled at working across global teams and managing multiple priorities.
As a Veteran-Owned company, we get you. We know what it's like to serve and come back, and we understand the value your skills hold to employers.
Questions about a job posting? Current employee inquiry? Submit the form below and we will expedite your request to the correct team member.
Provide strong technical expertise and engineering support for the design and development of both new and existing products. This includes addressing product quality, manufacturing efficiency, supply continuity, and cost optimization
Pay: $50/hr. – $54/hr.
Location: Franklin Lakes, NJ 07417 (On-site)
Duration: 12-month contract with possible extension
Relocation Assistance: Not available
Eligibility: Must be authorized to work in the U.S. without requiring sponsorship
The Product Development Engineer II provides technical expertise and engineering support for the design and development of both new and existing products. This role focuses on product quality, manufacturing efficiency, supply continuity, and cost optimization while ensuring compliance with regulatory standards.
Support design and development activities across new and legacy products.
Resolve issues related to product quality, manufacturing efficiency, and cost effectiveness.
Collaborate on cross-functional teams, providing timely and accurate technical input.
Propose innovative product concepts and enhancements.
Gather customer insights through literature reviews, interviews, observations, and competitive analysis.
Translate customer and business requirements into engineering specifications and designs.
Develop robust, manufacturable solutions using sound engineering principles.
Design and execute validation test methods, including test setup, measurement systems analysis, and data analysis.
Prepare detailed technical documentation to support design verification, changes, and regulatory requirements.
Bachelor’s degree in Engineering (Mechanical or Biomedical Engineering preferred).
2–4 years of engineering experience, ideally in the medical device industry.
Experience with Design Control, Risk Management, Quality, and Regulatory requirements.
Injection molding (plastics) knowledge strongly preferred.
Proficiency in statistical tools and computer-based analysis.
Strong problem-solving skills with ability to apply engineering fundamentals to practical challenges.
Our client, a Global Fortune 50 organization and one of the world’s largest distributors of healthcare systems, medical supplies & pharmaceutical products, seeks an accomplished Sr Technology Sourcing Procurement Manager.
Pay: $55/hr. – $59/hr.
Location: Richmond VA, Atlanta GA or Dallas TX (Remote)
Duration: 8-month contract (possibility of extension or conversion to FTE)
Work Type: Remote (with occasional travel for team meetings or supplier engagement)
Eligibility: Must be authorized to work in the U.S. without requiring sponsorship
We are seeking a high-performing and detail-oriented Senior Manager to support contract separation and sourcing efforts as we establish a new, independent business unit. This role will work closely with the Interim Strategic Sourcing Lead to manage supplier transitions, execute technology sourcing initiatives, and build a future-state indirect procurement model. The ideal candidate brings strong hands-on sourcing expertise—particularly in technology—and proven experience navigating contract disentanglement within complex enterprise agreements.
End Goal: Ensure the new standalone business is fully operational by May 1, 2026, with its own indirect procurement model and supplier agreements, while reducing value leakage, minimizing rework, and supporting team balance.
Our client, one of the largest Energy companies in the US providing a wide range of Energy-related products and services to its customers, seeks an accomplished Project Administrative Coordinator.
Pay: $25/hr. – $30/hr.
Location: Pearl River, NY 10965 (Hybrid)
Duration: 26-week contract (possibility of extension)
Work Hours: Monday–Friday, 6:30am–3:00pm or 7:00am–3:30pm (schedule determined by hiring manager)
Work Type: Onsite
Eligibility: Must be authorized to work in the U.S. without requiring sponsorship
The Animal Care Technician is responsible for animal husbandry, sanitation, health monitoring, and record-keeping in a biomedical research environment. This role ensures the highest standards of care and compliance with regulatory requirements.
Our client, a Global Fortune 50 organization and one of world’s largest distributors of Health care systems, medical supplies & Pharmaceutical products, seeks an accomplished “Pharmacist”.
Pay: $55/hr. – $60/hr.
Location: Fort Worth, TX 76177 (On-site)
Duration: 12-month contract with possible extension
Relocation Assistance: Not available
Eligibility: Must be authorized to work in the U.S. without requiring sponsorship
The Product Development Engineer II provides technical expertise and engineering support for the design and development of both new and existing products. This role focuses on product quality, manufacturing efficiency, supply continuity, and cost optimization while ensuring compliance with regulatory standards.
Support design and development activities across new and legacy products.
Resolve issues related to product quality, manufacturing efficiency, and cost effectiveness.
Collaborate on cross-functional teams, providing timely and accurate technical input.
Propose innovative product concepts and enhancements.
Gather customer insights through literature reviews, interviews, observations, and competitive analysis.
Translate customer and business requirements into engineering specifications and designs.
Develop robust, manufacturable solutions using sound engineering principles.
Design and execute validation test methods, including test setup, measurement systems analysis, and data analysis.
Prepare detailed technical documentation to support design verification, changes, and regulatory requirements.
Bachelor’s degree in Engineering (Mechanical or Biomedical Engineering preferred).
2–4 years of engineering experience, ideally in the medical device industry.
Experience with Design Control, Risk Management, Quality, and Regulatory requirements.
Injection molding (plastics) knowledge strongly preferred.
Proficiency in statistical tools and computer-based analysis.
Strong problem-solving skills with ability to apply engineering fundamentals to practical challenges.
Our client, a Medical Center facility under the aegis of a California Public Ivy university and one of largest health delivery systems in California, seeks accomplished Animal Technician.
Pay: $25/hr. – $27/hr.
Location: San Francisco, CA 94158 (On-site)
Duration: 26-week contract (possibility of extension)
Work Hours: Monday–Friday, 6:30am–3:00pm or 7:00am–3:30pm (schedule determined by hiring manager)
Work Type: Onsite
Eligibility: Must be authorized to work in the U.S. without requiring sponsorship
The Animal Care Technician is responsible for animal husbandry, sanitation, health monitoring, and record-keeping in a biomedical research environment. This role ensures the highest standards of care and compliance with regulatory requirements.
The Regulatory Affairs Specialist will be responsible for planning, coordinating, and implementing regulatory strategies for medical device products that require government approval. This role involves working closely with a global team (including Asia, Mexico, Korea, and Taiwan) and may require late afternoon calls. The position will start on-site before transitioning to a hybrid schedule.
Pay: $60/hr. – $70/hr.
Location: Irvine, CA, 92603 (On-site)
Duration: 18-month contract
Relocation/Interview Expenses: Not available
Work Arrangement: Onsite initially (5 days/week), transitioning to hybrid schedule
Eligibility: Must be authorized to work in the U.S. without requiring sponsorship
The Regulatory Affairs Specialist is responsible for planning, coordinating, and executing regulatory strategies for medical device products requiring government approval. This role involves collaborating with a global team across Asia, Mexico, Korea, and Taiwan and may require late-afternoon calls. The position begins onsite and will transition to a hybrid schedule.
Develop and implement regulatory strategies for products requiring approval or clearance.
Apply regulatory knowledge to support product submissions and compliance activities.
Prepare, review, and refine submission materials to meet regulatory standards.
Translate complex technical data into clear, reviewer-ready documentation.
Liaise with regulatory agencies to facilitate timely approvals.
Contribute to the strategic planning of regulatory pathways for new and existing products.
Retrieve and manage reports, protocols, and license transfers (over 6,000 documents) within Windchill.
Provide guidance and serve as a resource for less experienced colleagues.
Work independently with minimal supervision, effectively prioritizing tasks.
Education: Bachelor’s degree in Engineering (required).
1–2 years of regulatory affairs experience (medical device industry preferred).
Experience preparing regulatory submissions and ensuring compliance with requirements.
Familiarity with Windchill document management system (preferred).
Strong understanding of healthcare regulations and industry practices.
Ability to manage both routine and complex regulatory issues.
Excellent organizational, documentation, and communication skills.
Skilled at working across global teams and managing multiple priorities.
