1 - 20 of 160 Jobs

Quality Engineer II (QMS)

Sovereign Technologies

Irvine, California, USA

Contract

Note: This position is for W2 basis only Job Description: As a Quality Engineer II, you will be a key contributor to the implementation, maintenance, and continuous improvement of the Quality Management System (QMS) You will collaborate cross-functionally to ensure compliance with regulatory requirements, drive root cause investigations, and support quality initiatives that enhance product and process performance. Your role will be instrumental in ensuring that quality standards are embedded ac

Quality Engineer II (QMS Focus) - Medical

Kasmo Inc.

Irvine, California, USA

Contract

Description Quality Engineer II (QMS Focus) - Medical Location: Irvine, CA (Onsite) As a Quality Engineer II, you will be a key contributor to the implementation, maintenance, and continuous improvement of the Quality Management System (QMS). You will collaborate cross-functionally to ensure compliance with regulatory requirements, drive root cause investigations, and support quality initiatives that enhance product and process performance. Your role will be instrumental in ensuring that quality

Quality Management Systems (QMS) Engineer

Solventum

Columbia, Missouri, USA

Full-time

Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum. We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding. Please bear with us. In the interim, our Privacy Policy here: continues to apply to any personal information you submit, and the 3M-branded positions lis

Senior Veeva QMS Support Analyst

I.T. Solutions

San Francisco, California, USA

Contract

Sr. Veeva QMS Support Analyst San Francisco, CA Type: Contract Length: 3 months, maybe extensions Job Summary: We are seeking a detail-oriented and technically skilled Veeva QMS Support Specialist to provide end-user support, configuration assistance, and continuous improvement for our Veeva Quality Management System (QMS). This role serves as a bridge between Quality, IT, and end users, ensuring smooth implementation and operation of Veeva QMS modules including Change COntrol, Deviations (QE)

Quality Management Systems (QMS) and Cybersecurity Compliance Specialist

Dew Software

Massachusetts, USA

Third Party, Contract

Job Description: Seeking a skilled Quality Management Systems (QMS) and Cybersecurity Compliance Specialist to lead the integration and upgrade of our QMS, assist in internal cybersecurity audits, and provide regulatory submission support (FDA, EU) at our Boston site. The ideal candidate will bring a comprehensive understanding of quality management processes, document control, and corrective and preventive actions (CAPA), with experience supporting regulatory compliance initiatives. Key Respon

Benchling Consultant

DRC Systems USA LLC

Remote

Contract

Overview: Looking for Benchling Consultant for REMOTE roleJob Description :We need someone to provide Benchling Application Support, candidate must have experience in providing technical support for Benchling application, addressing queries related to Benchling, ensuring a seamless user experience and compliance with QMS standards Experience in creating / updating Benchling templates, preparing training materials, automation using Python will be added advantage

Manufacturing Associate

Zachary Piper Solutions, LLC

Durham, North Carolina, USA

Full-time

Piper Companies is seeking a Manufacturing Associate for an on-site contract position in Durham, North Carolina (NC). The Manufacturing Associate you will be integral to our production team, ensuring the efficient operation of manufacturing equipment and adherence to quality standards. Responsibilities of the Manufacturing Associate include: Oversee and operate biopharmaceutical manufacturing equipment. Adhere to SOPs and GMP guidelines to uphold product quality standards. Gain cross-trainin

Sr. QA Manager

Zachary Piper Solutions, LLC

Chelmsford, Massachusetts, USA

Full-time

Piper Companies is seeking a Senior Quality Assurance Manager to lead quality assurance efforts for a medical device facility in Chelmsford, MA through a M-F Onsite work schedule. The Senior Quality Assurance Manager is pivotal in ensuring compliance with regulatory standards and driving continuous improvement initiatives. Responsibilities of the Senior Quality Assurance Manager include: Lead quality assurance for two products: balloon pump and balloon catheter. Develop and execute QA strategie

Senior Quality Assurance Manager

Zachary Piper Solutions, LLC

Chelmsford, Massachusetts, USA

Full-time

Piper Companies is seeking a Senior Quality Assurance Manager to lead quality assurance efforts for a medical device facility in Chelmsford, MA through a M-F Onsite work schedule. The Senior Quality Assurance Manager is pivotal in ensuring compliance with regulatory standards and driving continuous improvement initiatives. Responsibilities of the Senior Quality Assurance Manager include: Lead quality assurance for two products: balloon pump and balloon catheter. Develop and execute QA strategie

Solutions Porgram Manager

Gardner Resources Consulting, LLC

Remote

Contract

Solutions Program Manager Required Skills and Competencies: SDLC and Infrastructure Program Management experience Agile/SAFe certification and transformation experience Project management certification preferred Experience leading development, testing, and launch of hardware, software, and cloud systems Experienced working with Agile teams to develop and launch strategic programs against concreate deadlines Knowledge of computer systems validation and QMS compliance Demonstrated flexibility and

Veeva Senior Support Engineer

Katalyst Healthcares and Lifesciences

Indianapolis, Indiana, USA

Full-time

Job Description: We are looking for candidate over 5 years of experience with Veeva Vault QMS, demonstrating a strong understanding of quality management processes and a proven track record in support roles, handling technical issues and user queries. Excellent communication and collaboration skills are essential, enabling effective work both independently and as part of a team. Additionally, knowledge of regulatory requirements in the healthcare industry is a plus. This role is perfect for som

Process Validation Engineer

Katalyst Healthcares and Lifesciences

Albany, Georgia, USA

Full-time

Responsibilities: Spearhead qualification protocols for next-generation manufacturing processes. Drive manufacturing investigations and implement innovative solutions. Design validation strategies for new product launches and technology transfers. Lead comprehensive IQ/OQ/PQ validation activities across multiple projects. Create robust standard operating procedures for manufacturing excellence. Ensure continuous process verification for robust manufacturing operations. Coordinate cross-fu

Validation Engineer

Zachary Piper Solutions, LLC

Lynwood, California, USA

Full-time

Piper Companies is currently seeking an experienced Validation Engineer tosupport a highly reputable Pharmaceutical company in Lynwood, California. Responsibilities for the Validation Engineer Oversee validation activities, including risk analysis, packaging, cleaning, and equipment qualification for new and updated processes.Develop, review, and execute validation protocols, reports, and documentation while ensuring compliance with GMP standards.Coordinate validation efforts across shifts, pr

Systems Engineer

Katalyst Healthcares and Lifesciences

Skaneateles, New York, USA

Full-time

Responsibilities: Responsible for integration of design and manufacturing process procedures, templates and guidance documents within an ISO 13485 compliant Quality Management System (QMS). Demonstrated ability to communicate with a wide set of stakeholders (Quality, Systems/Risk, PM, RA, Marketing, etc.). Demonstrated understanding of the end-to-end process of identifying stakeholder needs, translation to Design Inputs and tracing these to the Design Outputs. Demonstrated understanding of Syste

Quality Control Manager

Zachary Piper Solutions, LLC

Wayne, Pennsylvania, USA

Full-time

Piper Companies is seeking a Quality Control Manager to join a reputable Biologics Quality Control Testing company located in Wayne, Pa. Responsibilities of the Quality Control Manager include: Lead projects, collaborate with clients and teams, and ensure expectations are met Oversee testing, manage deviations, and ensure adherence to global regulations Represent the team in audits, address issues, and implement corrective actions Manage assay development, validation, and ongoing compliance

Validation Engineer II

Zachary Piper Solutions, LLC

Lynwood, California, USA

Full-time

Piper Companies is seeking an experienced Validation Engineer II to support a highly reputable Pharmaceutical company in Lynwood, California. Responsibilities: Responsible for risk analysis, packaging validation, cleaning validation, and equipment qualification required for new products, processes, and equipment and any changes to existing products, processes, and equipment. Provide recommendations for product disposition or other actions related to product and equipment performance issue

Project Manager with IQMS or DELMIAworks Experience - M

Next Step Systems

Boyertown, Pennsylvania, USA

Full-time

Project Manager with IQMS or DELMIAworks Experience We a seeking a Project Manager for a great opportunity in Boyertown, PA. The Project Manager in this position is to report to and receive directions from the Director, Information Technology. The role is based in Boyertown, PA, and requires 3 days Onsite (Tuesday, Wednesday, Thursday). Willingness and ability to travel up to 25% (1-2 times every 2 months). Project Manager Responsibilities: - The Project Manager will manage the daily operatio

Associate Director IT Compliance & Governance

Zachary Piper Solutions, LLC

Conshohocken, Pennsylvania, USA

Full-time

Piper Companies is currently looking for an experienced Associate Director of IT Compliance & Governance in Conshohocken, Pennsylvania (PA) to work for an innovative and growing pharmaceutical manufacturer. Responsibilities for the Associate Director of IT Compliance & Governance include: Maintain the Technology Compliance Framework aligned with global regulations, organizational risks, and evolving guidance and industry standards. Lead implementation and maintenance of IT Policy & SOPs in suppo

Validation Engineer, Sterile & Cleaning

Katalyst Healthcares and Lifesciences

Bedford, Massachusetts, USA

Full-time

Responsibilities: We are seeking an experienced Sterile & Cleaning Validation Engineer to support validation activities within a medical device manufacturing environment. The ideal candidate will have hands-on experience with sterile and cleaning validation processes, strong technical writing skills, and the ability to execute validation protocols independently. This role involves performing revalidation tasks for equipment and working closely with cross-functional teams. Develop and execute

Quality Inspector

Motion Recruitment Partners, LLC

Meriden, Connecticut, USA

Full-time

Job Description: We are seeking a Quality Inspector for our client in Meriden, CT. We are looking for a detail-oriented professional who will be responsible for the development, implementation, and maintenance of inspection activities. Someone able to detect and be part of the resolution of problems. Ensures that the product integrity and quality standards are being met. Monitors, supports and helps improve the Quality Management System (QMS). Helps to create and maintain a positive and eff