Payrate: $50.50 - $52.58/hr. Summary: The Supply Chain Project Manager (SCPM) will translate product variation strategy as determined by the Variation Lead for reportable changes for Global Distribution control. May also translate product launch/variation strategy as determined by the Regional Operations Lead to an executable implementation plan for launch/variation changes for Customer Facing SKU control. This role will owe the execution of the implementation plan in terms of project management

RESPONSIBILITIES: Kforce has a client that is looking for a Remote IT Change Control Manager (Pacific/Mountain Time). This company is a well-established leader in their industry for over 50 years and is continuing to grow. Summary: The Change Control Manager plays an important role in the organization by performing several activities related to the company's Information Technology Change Management functions. The position will primarily be responsible for controlling and auditing changes to pro

Roles & Responsibilities: Minimum 7 years of CQV experience in a parenteral fill/finish environment. Lead process validation projects of broad scope. Responsible for project deliverables such as VMPs, pFMEAs, PPQ protocols and reports, change control assessments, technical transfer assessments, as well as other client deliverables as required. Provide technical support to Manufacturing - troubleshooting and resolving process related issues. Participate in investigations and provide documentation

Job Title: Sr Automation Engineer Location: Rahway, NJ (100% Onsite) Duration: 3 months with indefinite extensions Pay Rate: $50/hr-$70/hr (depending on experience) Job Description: Seeking a senior automation controls engineer with experience with Delta V preferably v14. Will be involved in handling multiple projects that include changes/enhancements to the hardware and software Need an automation engineer with experience in programming to customize the modules PLC Programming experience Must

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)

Responsibilities: Ask candidates if they have validated equipment and what type of equipment they have validated. Mechanical/manufacturing experience. Writing and executing validation protocols. CSV is nice to have, but if the candidate has done that exclusively it will not work. Requirements: A minimum of a Bachelor's degree in Engineering is required. Minimum of 1-3 years' experience in medical device manufacturing, Bio/pharma is also good Develop and implement processes to support the

Responsibilities: Perform Smoke studies and assist in semiannual Media fill qualifications as a SME Perform requalification/periodic review of autoclaves, depyrogenation tunnels, cold rooms, freezers, and warehouse areas. Has worked with Ellabs data loggers and software. Write and execute protocols and complete final reports. Understanding of cleaning validation concepts and principles. Understands pharma grade utilities (water HVAC, gases). Requirements: Support Maintenance, Engineering

Roles & Responsibilities: Lead process validation projects of broad scope. Collaborate with clients, Validation, and cross-functional team members to coordinate projects, resolve issues, and meet aggressive timelines. Represent Validation in customer interactions and communicate customer requirements to the broader Validation team as needed. Oversee execution of process validation (PPQ) protocols on the production floor on varying shifts as needed to ensure that protocol requirements are satisfi

Piper Companies is seeking a Deviation Management Consultant to fill an opportunity with a reputable Pharmaceutical company in Lansdale, PA. Responsibilities: Investigate deviations by assessing product impact, identifying root causes, and implementing corrective/preventative actions. Author and update GMP documentation, including SOPs, batch records, validation documents, and change controls. Write quality incident and deviation reports, ensuring thorough analysis and compliance. Collabor

Title: IT Program Manager VLocation: Northeastern United States (Onsite)Employment Type: ContractCompensation Pay Range:$40.16-$58.01/HrsDescription: * Drive successful delivery of key technology projects in the credit risk technology space. * Capture and support the delivery of business requirements. * Work with development teams to implement technology changes. * Remediate risks and issues to ensure end-to-end delivery of key initiatives. * Maintain organization and manage multiple projects an

Piper Companies is seeking a Deviation Management Specialist to fill an opportunity with a reputable Pharmaceutical company in Lansdale, PA. Responsibilities for the Deviation Management Specialist Investigate deviations by assessing product impact, identifying root causes, and implementing corrective/preventative actions. Author and update GMP documentation, including SOPs, batch records, validation documents, and change controls. Write quality incident and deviation reports, ensuring thoro

Title: Interface AnalystEmployment Type: Contract W2 onlyCompensation: Pay rate: $50-$90/hrDescription * Design, develop, and support HL7 interfaces within the EPIC environment. * Collaborate with external vendors and internal teams to ensure data integration. * Monitor interface performance and troubleshoot issues. * Maintain interface documentation and change control. * Support data integrity and interoperability standards.Key Responsibilities * Configure and maintain interfaces in EPIC Bridge

Responsibilities: Our client is currently in the process of starting up a clinical cell therapy site with clean rooms. They are in the commissioning phase and validating documentation and processes for the utilities, facilities, computer systems, and cleanroom environments to meet the requirements for cell-based therapies. The site will be designed to support the production of cell therapies, which necessitates adherence to GMP, regulatory compliance, and the implementation of validation and com

Job Description: The team developing industry leading X-ray tubes for clinical applications is looking for highly motivated Mechanical Engineers to join them to enhance the quality & performance of X-ray tubes. Mechanical Engineer will be working on fixture design and testing of X-ray tube sub-assemblies to enhance robustness and performance. Responsibilities: Mechanical design utilizing Creo / Windchill. Simulation / analysis (Creo / Ansys FEA, stack up analysis) and testing in the lab. Desi

IT Program Manager Locations: - Jersey City, NJ ( Not more than 45 miles) Hybrid/ Onsite: Hybrid Note from hiring manager somebody with a strong Project Manager with credit risk, Capital market experience and Business analyst with Banking clients. PM is required to help drive the successful delivery of key technology projects in the Counterparty Credit Risk Technology space. Capturing and supporting delivery of business requirements, working with dev team to implement technology changes, remed

Job Title: Engineering Services Analyst Location: Onsite Mountain View, CA Contract Duration: 6 Months Only for those who would not require sponsorship now or in future and can work on W2 contract. Top 3 Required Skills Expertise in PLM/PDM systems and document controlStrong organizational and communication skillsBackground in engineering services or outsourced manufacturingKey Responsibilities Document & Change Control Manage and distribute engineering documentation to teams and suppliersOwn th

The Management and Systems Engineer's duties include: Assists in the development and management of requirements for nuclear infrastructure project delivery. Assembles and manages definition of high-level requirements to satisfy customer and project end goals. Manages and oversee the development of derived requirements as developed during early design definition. Management of Contract and SOW requirements Communicates in a manner that is consistent, effective, and efficient in both written and

Key Responsibilities: Manufacturing Support: Develop technical knowledge on manufacturing equipment and processes Support resolution of major equipment breakdowns and quality issues in the suites Provide SME support to Manufacturing and other departments for the design and operation of process equipment. Conduct troubleshooting and technical analyses on manufacturing equipment and processes including PI data analyses, CIP/SIP circuit review, MOC analyses, flow path analyses, etc. Projects : Pla

Title: IT Project Analyst (Financial Services) Location: Jersey City - 07311 (4 days on-site) Duration: 12+ month contract Compensation: $40-42/hr. Work Requirements: , Holders, or Authorized to Work in the U.S.Experience: 2-5 years of experience in IT project management in the financial industry is preferred. Project governance/project budgeting is highly desired. Attention to detail is a MUST - daily validation of numbers and dates is required.Responsibilities: Focus on reviewing and approvi

Responsibilities: Lead the development and execution of commissioning, qualification, and validation protocols for a range of laboratory equipment, facility systems, and utilities. Draft, review, author, and deploy all required validation documentation including IQ/OQ/PQ protocols, reports, master plans, risk assessments, procedures, reports, and so on. Provide technical expertise throughout the validation lifecycle including risk assessment, deviation investigation, and change control activiti