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Entry Level Qms Implementation Jobs (NOW HIRING)

Triman Industries Inc

Quality Technician 1

Yonkers, NY · On-site

$52K - $60K/yr

BASIC FUNCTIONS Entry level position. Performs basic counterfeit lab testing and visual inspection ... Review and implement detailed inspection reports to provide all information regarding product ...

Abbott

Quality Engineer I

Los Angeles, CA

$77.60K - $100.20K/yr

WHAT YOU'LL DO - Identify and implement effective process control systems to support the ... QMS), Environmental Management Systems (EMS), and other regulatory requirements - Complies with U.S.

Abbott

Quality Engineer I

Los Angeles, CA

$77.60K - $100.20K/yr

WHAT YOU'LL DO - Identify and implement effective process control systems to support the ... QMS), Environmental Management Systems (EMS), and other regulatory requirements - Complies with U.S.

Abbott

Quality Engineer I

Sylmar, CA · On-site

$73.20K - $94.50K/yr

WHAT YOU'LL DO - Identify and implement effective process control systems to support the ... QMS), Environmental Management Systems (EMS), and other regulatory requirements - Complies with U.S.

AMERICAN SYSTEMS

Mechanical Designer/Drafter I

Norwich, CT · On-site

$25 - $28/hr

Overview The Mechanical Designer/Drafter I is an entry-level position that supports mechanical ... Implement Standard Geometric Dimensioning and Tolerancing (GD&T) practices in accordance with ASME ...

American Systems

Mechanical Designer/Drafter I

Norwich, CT

$44.30K - $73.90K/yr

... entry-level position that supports mechanical design and drafting efforts for United States Navy ... Implement Standard Geometric Dimensioning and Tolerancing (GD&T) practices in accordance with ASME ...

Shield Restraint Systems Inc.

Quality Engineer

Elkhart, IN · On-site

$80K - $100K/yr

About This Opportunity We're seeking a motivated professional to join our team in an entry-level ... Support the implementation of good GD&T practice and component tolerance methodology on new ...

Abbott

Extrusion Manufacturing Engineer II

Plymouth, MN · On-site

$61.30K - $122.70K/yr

Develop and implement process improvements. * Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS ...

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How much do entry level qms implementation jobs pay per hour?

As of May 31, 2026, the average hourly pay for entry level qms implementation in the United States is $51.41, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $61.06 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Entry Level QMS Implementation specialist, and why are they important?

To thrive as an Entry Level QMS Implementation specialist, you need a foundational understanding of quality management principles, process documentation, and relevant regulations, often supported by a degree in engineering, life sciences, or a related field. Familiarity with QMS software tools, ISO 9001 standards, and basic auditing techniques is typically required. Strong attention to detail, analytical thinking, and effective communication help you excel in coordinating with teams and ensuring compliance. These skills ensure the smooth rollout and maintenance of quality management systems, which are critical for regulatory adherence and operational efficiency.

What are some common challenges faced when starting as an Entry Level QMS Implementation specialist, and how can they be overcome?

Entry Level QMS Implementation specialists often encounter challenges such as understanding complex regulatory requirements, adapting to different organizational processes, and encouraging staff to adopt new quality procedures. Building a solid foundation by actively seeking training and mentorship helps in grasping the essential standards like ISO 9001. Open communication and collaboration with cross-functional teams are key to successful implementation and overcoming resistance to change. Documenting each step and seeking feedback regularly will also support a smoother transition and continuous improvement.

What is an Entry Level QMS Implementation role?

An Entry Level QMS (Quality Management System) Implementation role involves assisting organizations in setting up and maintaining quality management systems, such as ISO 9001. Professionals in this position help document processes, conduct audits, and ensure compliance with industry standards under the guidance of senior staff. They may also provide support in training employees, tracking corrective actions, and maintaining quality records. This role is ideal for individuals starting their careers in quality assurance or regulatory compliance.

What is the difference between Entry Level Qms Implementation vs Quality Assurance Technician?

AspectEntry Level Qms ImplementationQuality Assurance Technician
CertificationsISO 9001, basic QMS trainingISO 9001, Six Sigma Green Belt (optional)
Work EnvironmentOffice, manufacturing, or production settingsManufacturing plants, labs, or production lines
Employer & Industry UsageManufacturing, aerospace, automotive, medical devicesManufacturing, electronics, pharmaceuticals
Primary FocusImplementing and maintaining QMS processesTesting, inspecting, and ensuring product quality

Entry Level Qms Implementation roles focus on establishing and supporting quality management systems, often involving process documentation and compliance. Quality Assurance Technicians primarily perform product testing and inspections to ensure quality standards. While both roles support quality objectives, Qms Implementation is more process-oriented, whereas QA Technicians focus on product verification.

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Entry Level Qms Implementation jobs near you
Supplier Quality Engineer

Supplier Quality Engineer

Katalyst Healthcares & Life Sciences

Sunnyvale, CA

Contractor

Posted 10 days ago

Job description

Company Description
  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.
Job Description

Responsibilities:

  • Select and evaluate suppliers by leading efforts to find new suppliers in an existing or new commodity.
  • Conduct on-site supplier assessments as well as QMS audits and address the non-conformities.
  • Work with suppliers and ISI engineering for the new product introduction to
  • Complete part production qualification process ( PPQP), which includes but not limited to delivering on the following deliverables: spFMEA, Special Process Validations, Process capability, MSA, capacity analysis, and FAIR.
  • Develop supplier ramp readiness based on forecast, supplier capacity, quality performance, and process capability.
  • Perform DFM by engaging suppliers early in development cycle to feedback manufacturability improvements in the designs prior to production.
  • Lead and resolve the supply continuity/ quality issues at suppliers through in depth root cause and corrective actions utilizing SCARs, SCRs (Supplier Change requests) processes.
  • Monitor supplier performance and initiate improvement activities.
  • Drive suppliers to continually improve their business and manufacturing process performance to meet Intuitive Surgical's requirements for supplier excellence including ship to stock programs using a collection of best practices in project management, Six Sigma, Lean, SPC and negotiation by leading these efforts without managerial guidance at several suppliers simultaneously.
  • Develop and use metrics for supplier part cost, delivery, quality, capacity and capability by creating metrics to measure real improvement and judge required intervention or change at the supplier or in a commodity.
  • Driving change to ISI specifications as necessary by understanding and changing specifications and drawings including driving the ECO process to implementation.
  • Prepare and deliver supplier communications as required by independently working with suppliers on scorecard creation of QBRs, Supplier Summits, etc.
  • Identify and investigate opportunities for cost reduction and/or quality improvement by judging opportunities and creating strategies to seize those opportunities, completes research and provides data-driven plans to management.

Requirements:

  • BS degree in Engineering or equivalent, master's degree preferred.
  • Excellent knowledge of 21 CFR part 820 and ISO 13485 (experience in auditing suppliers to these standards): Certified Lead auditor preferred but not required.
  • Practical knowledge of PFMEA's and process validations.
  • Ability to read and interpret detailed mechanical drawings and communicate technical information.
  • Excellent problem solving and project management skills.
  • Excellent written and verbal communication skills including presentations to executive level management.
  • A proven history of implementing Lean/6 Sigma/SPC Programs at suppliers.
  • Practical knowledge of part production qualification process.
  • Significant computer experience using Windows, Word, Excel, Access and ERP Information Systems, preferably SAP.
  • CAD experience with 3D modelling tools is a plus.
  • Experience in a high-volume medical device company is a plus.
  • Ability to travel to suppliers on an as needed basis - domestic and international.
Additional Information

All your information will be kept confidential according to EEO guidelines.

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About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

Social media

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