1 - 20 of 125 Jobs

Validation Lead

TechDigital Corporation

King of Prussia, Pennsylvania, USA

Contract, Third Party

Computer System Validation, Computed system assurance, GAMP, GxP risk assessments, Change Management 10+ years' Experience in Validating systems and Experienced in CSV activities in GxP related applications like SAP Systems, Product Serialization systems, MES systems Perform review for GxP systems to ensure compliance with regulatory requirements Working knowledge on end-to-end validation of GxP applications and is able to perform document/process Compliance Analysis Adept with Agile and Waterf

Quality Manager

Advantage Technical

McChesneytown-Loyalhanna, Pennsylvania, USA

Full-time

Quality Manager Direct Hire Location: Loyalhanna, PA Pay: $92K to $120K (plus bonus) Job Description: Establish procedures for maintaining high standards of quality, reliability, and safety. Determine and enforce quality and safety requirements in accordance with real company needs, based on current regulations and product development. Organize and promote companywide quality improvement efforts. Evaluate and develop improved techniques for the control of quality, reliability, and safety. D

Principal Nitinol Engineer

Manpower Engineering

Saint Paul, Minnesota, USA

Full-time

A well-established medical device client of ours within the Twin Cities is seeking a Principal Nitinol Engineer to be a technical lead over the nitinol business unit within their organization. Candidates should have an extensive background within medical device manufacturing especially within the nitinol space. This direct hire role will be based out in the Twin Cities Metro Area. Job Title: Principal Nitinol Technical Lead Engineer Location: Fridley, MN Salary: 125-160k Position Responsibili

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

Qaudient Sr. Developer

Stanley David and Associates

Newark, New Jersey, USA

Full-time

Role: Qaudient Sr. Developer Location: Newark, NJ (Onsite) Must Have Technical/Functional Skills At least 8+ years experience in Quadient InspireWorking experience in Quadient Inspire Designer, Quadient Inspire Automation, Quadient Inspire Scaler, Quadient Inspire Content Manager, Quadient Inspire Interactive is required.Experience is working on QMS model of Quadient.Experience in data input, data-processing, Layout Design, Imposition, and output modules of Inspire DesignerExperience / Exposure

Configuration Manager

Judge Group, Inc.

Bristol, Pennsylvania, USA

Full-time

Location: Bristol, PA Salary: $55,000.00 USD Annually - $60,000.00 USD Annually Description: Our client is currently seeking a Configuration Management Assistant for a full-time position. Control and manage all product and Quality Management System (QMS) documentation related to the design and manufacturing required to support compliance. Documentation such as: Product requirements, specifications, technical drawings, procedures, work instructions, manufacturing routings, Product Bill of M

Quality Engineer

Jobot

Louisville, Kentucky, USA

Full-time

Quality Engineer This Jobot Job is hosted by: Christopher Singleton Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $85,000 - $110,000 per year A bit about us: Permanent on-site Management position! Why join us? Competitive Base Salary! Extremely Competitive Equity Package! Flexible Work Schedules! Accelerated Career Growth! Job Details Job Details: We are seeking a highly motivated and experienced Permanent Quality Manager to join our

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

PTC Windchill PLM Developer

eQuest Solutions

Remote

Full-time

Position is 100% Remote Please note I have direct access to the Hiring Director on this position. Compensation: Base Salary + Bonus This is an outstanding opportunity for a Windchill Developer to be involved in a large-scale global rollout, implementation and feature expansion and enhancements of Windchill PLM, QMS and ThingWorx on Windchill+. We are the leading Global Biotech Company in our niche and are looking for a 100% Remote PTC Windchill Developer/Configurator due to company expansion. We

Project Manager with IQMS or DELMIAworks Experience - G

Next Step Systems

Boyertown, Pennsylvania, USA

Full-time

Project Manager with IQMS or DELMIAworks Experience, Boyertown, PA 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

Solution Architect with SAP integration experience

Axiom Global Technologies, Inc.

Remote

Contract

Role: Solution Architect with SAP integration experience Location: Any Client hub Duration: 3-6 Months Solution Architect who will be responsible for designing technology solutions and integrations that meet the business needs of our client. This role requires a deep understanding of SAP configuration, integrations with ERP, PLM, and QMS systems, strong technical skills, and the ability to communicate effectively with stakeholders. Collaborate with business stakeholders to understand their requi

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

Sr Quality Engineer @ Tamarac, FL

Amzur Technologies, Inc.

Tamarac, Florida, USA

Full-time

Sr Quality Engineer Location: Tamarac, FL Duration: Permanent Preferred: Training and basic understanding of Lean Manufacturing and/or Six Sigma is desired. Experience in conducting Supplier Quality and/or Internal Audits is desired. Education: Bachelor s degree in Engineering. General Overview: The Quality Engineer develops, establishes, and maintains quality systems and processes that meet company and customer needs. This position provides focused quality engineering support of manufacturing

Quality Management Systems (QMS) Specialist (W2)

Sovereign Technologies

Irvine, California, USA

Contract

Title: Document Control Coordinator - QMS Location: Irvine, CA Onsite Document Control Specialist QMS Job Description We are seeking a dedicated Quality Management Systems (QMS) Specialist who will play a crucial role in ensuring compliance with internal and external regulatory requirements. This role involves engaging in the development of future state QMS for business needs, executing modifications, and contributing to the quality planning process. Responsibilities Ensure QMS compliance with a

Technical Writer - Pittsburgh, PA - $70k per annum - fulltime

MetaSense, Inc.

Pittsburgh, Pennsylvania, USA

Full-time

PRINCIPAL RESPONSIBILITIES: 2+ years of experience as a Technical Writer (for SOP, QMS etc.) in the medical device industryPractical knowledge of standards and regulations pertaining to the medical device industry.Experience with CAD and VisioYou will be trained on client products and SOPs / templatesMaintain a backlog of all change requests to client's QMS design controls procedures/WIs/forms, in response to CAPAs or for efficiency improvements.Plan and execute the defining the specific procedu

Quality Engineer

NasTech Global, Inc.

Tamarac, Florida, USA

Full-time

Job Title: Quality Engineer Location: Tamarac, FL(Onsite) Job Type: Direct Hire Must-Have: Experience with Lead Six Sigma Green Belt Experience as a QE - at least 1 full year Basic statistical methods like trend analysis Attention to detail and timeliness Analytical Excellent communication skills Experienced in quality management systems (QMS) Writing procedures and work instructions MS Office experience to include Word, Excel, and PP Experience with corrective and preventive actions

Service and Rental Manager

Manpower

Minneapolis, Minnesota, USA

Full-time

Job DescriptionJob DescriptionService and Rental Manager Our client in Blaine, MN is looking for hardworking, motivated Service & Rental Manager to join their team. Don t wait apply today! What You ll Do Evaluate rental fleet usage and order new equipment as necessary and sell outdated used equipment.Monitor & direct Associates and Technicians performance of day-to-day department tasks.Ensure adherence & participate with ISO 9001 QMS system.Track and maintain machine and parts inventory.Plan fu

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

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

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