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CQV Engineer

Katalyst Healthcares and Lifesciences

Pennington, New Jersey, USA

Full-time

Responsibilities: Prepare commissioning, qualification, and validation documents for equipment, utilities, and systems. Verify that systems and equipment operate according to design specifications and regulatory requirements. Prepare and maintain comprehensive validation documentation, including test protocols, reports, and standard operating procedures. Work closely with engineering, quality assurance, and production teams to resolve issues related to CQV. Implement corrective actions and impro

Validation Engineering

Katalyst Healthcares and Lifesciences

Marlborough, Massachusetts, USA

Full-time

Responsibilities: TCU Mapping Protocols: Conduct and document temperature mapping activities to ensure that Temperature Control Units (TCUs) comply with regulatory and operational standards. Protocol Support: Assist in the development and execution of validation protocols, ensuring alignment with both internal and regulatory requirements. Data Collection & Analysis: Support the collection and initial analysis of TCU mapping data to aid in validation reporting and quality control. Collaboration

Cerner RIS Analyst

TechDigital Corporation

Remote

Contract, Third Party

"Responsibilities: A Cerner RIS (Radiology Information System) and PACS (Picture Archiving and Communication System) Analyst is responsible for managing and maintaining these critical systems in a healthcare setting. Here are some key responsibilities and requirements for this role 1. System Management: Oversee the daily operation and maintenance of RIS and PACS systems, ensuring they run smoothly and efficiently. 2. Data Management: Handle data archiving, storage, and retrieval, ensuring compli

Owner's Rep Project Manager - Healthcare Architecture & Engineering

Jobot

Charleston, South Carolina, USA

Full-time

Project Manager - Healthcare Architecture & Engineering | $85K-$110K | General Contractor or Design/Engineering Backgrounds Welcome This Jobot Job is hosted by: Augie Ullmann 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: Founded nearly a decade ago and based in the Greater Philadelphia area, we are a fast-growing construction management firm specializing in high-impact, highly regulated projects

Validation Engineer

Katalyst Healthcares and Lifesciences

Richmond, Virginia, USA

Full-time

Responsibilities: Develop and implement comprehensive validation plans for packaging lines, labelers, case packers, and low-speed pen assembly. Lead the validation of various systems, including SEA Vision Yudoo and AVI systems, ensuring compliance with industry standards and regulatory requirements. Prepare, execute, and document Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Validation Summary Reports (VSR). Collaborate with cross-functi

Validation Engineer

Katalyst Healthcares and Lifesciences

Richmond, Virginia, USA

Full-time

Responsibilities: Develop and implement comprehensive validation plans for packaging lines, labelers, case packers, and low-speed pen assembly. Lead the validation of various systems, including SEA Vision Yudoo and AVI systems, ensuring compliance with industry standards and regulatory requirements. Prepare, execute, and document Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Validation Summary Reports (VSR). Collaborate with cross-functional

Microsoft Dynamics 365 CRM Technical

ETS LLC

New York, New York, USA

Contract

Role name: Consultant Role Description: Key Responsibilities:Lead the discovery, evaluation, and selection of a Patient Services CRM platformCollaborate with Commercial, IT, Patient Services, and Compliance teams to document current-state workflows and define future-state requirementsAssess platform capabilities across Salesforce Health Cloud, Veeva CRM, Pega, and Courier HealthDevelop functional and technical evaluation criteria and scoring matricesParticipate in vendor demos, stakeholder works

Regulatory Solutions Architect

INGENworks

Atlanta, Georgia, USA

Contract

Regulatory Solutions Architect Location: RemoteDuration: Long Term Required Qualifications:Bachelor s or Master s degree in Computer Science, Regulatory Affairs, Life Sciences, or a related field.7+ years of experience in Regulatory IT or Regulatory Affairs, including 3+ years as an Architect or Lead.Proven experience working with Commercial Regulatory Affairs systems (e.g., labeling, promotional compliance, Veeva PromoMats, MedComms).In-depth knowledge of regulatory requirements in US, EU, and

Workday Integration Consultant

Healthcare IT Leaders

US

Full-time

Healthcare IT Leaders is seeking an experienced Workday Integrations Consultant to join our dynamic team. In this role, you will be responsible for designing, developing, and supporting complex Workday integrations that connect our Workday modules with other enterprise systems. You will work closely with project teams, business stakeholders, and external vendors to ensure that integration solutions align with business requirements and industry best practices. Your technical expertise in Workday

Commissioning and Qualification Engineer

Katalyst Healthcares and Lifesciences

Raleigh, North Carolina, USA

Full-time

Responsibilities: Lead or support C&Q activities for pharmaceutical utilities and process equipment, ensuring compliance with industry standards and regulatory requirements. Execute FAT (Factory Acceptance Testing) to validate equipment functionality and performance. Support the qualification of Black and Clean utilities, such as water systems, clean steam, HVAC, and gas utilities. Perform process equipment qualification to meet GMP and production readiness standards. Develop and execute C&Q pro

Commissioning Qualification Validation Engineer

Zachary Piper Solutions, LLC

Durham, North Carolina, USA

Full-time

Piper Companies is currently looking for an experienced Commissioning Qualification Validation Engineer (CQV) in Raritan, New Jersey (NJ) to work for an innovative and growing pharmaceutical manufacturer. Responsibilities for the Commissioning Qualification Validation Engineer (CQV) include: Commissioning: Lead commissioning activities for new laboratory equipment, systems, and facilities, ensuring they are installed and function as intended. Qualification: Develop, execute, and document qualif

Maximo Consultant

Unique System Skills LLC

Norwood, Massachusetts, USA

Contract, Third Party

Job Title: Maximo Functional Consultant Location: Norwood, MA(Onsite day 1) Duration: 12+ months Bachelor s degree in computer science, Information Technology, Engineering, or a related field.Over 10 years of experience as a Maximo Functional Consultant or in a similar role.Extensive knowledge of IBM Maximo Asset Management, including implementation, configuration, and customization.Strong understanding of asset management processes and industry best practices.Proficiency in designing and config

Construction Project Manager (BioPharma)

Zachary Piper Solutions, LLC

Bloomington, Indiana, USA

Full-time

Piper Companies is seeking a BioPharma Construction Project Manager to manage the construction and communication of a new facility build for a CDMO out in Bloomington, IN. The role has an onsite expectation and slated through 2026 and potentially beyond. The Construction Project Manager will oversee the planning, execution, and delivery of our new facility buildout project in Bloomington, ensuring it is completed on time, within scope, and within budget. This is a high-impact role that requires

Validation Engineer

Katalyst Healthcares and Lifesciences

Nashville, Tennessee, USA

Full-time

Responsibilities: Ensure all manufacturing equipment (e.g., mixers, conveyors, packaging lines) undergoes: These confirm proper functionality and adherence to operational specifications. Validate manufacturing processes (e.g., blending, cutting, rolling, and packaging) to ensure consistent production of high-quality products. Conduct revalidation of equipment and processes when changes occur, such as: ssess risks related to equipment, processes, and production areas that could impact product qua

Senior Scientist, Cell Culture

Zachary Piper Solutions, LLC

Minneapolis, Minnesota, USA

Full-time

Piper Health & Sciences is hiring for a Senior Scientist, Cell Culture at a biotechnology organization in the Greater Minneapolis, MN area. This is a full-time, direct hire position with comprehensive benefits. Responsibilities for the Senior Scientist include: Design, optimize, and develop mammalian cell culture media formulations Work with primary cells and stem cells to advance cell-based research and therapies Lead experimental phases of complex R&D projects with a creative and strategic app

Environmental Monitoring Analyst - PM Shift (McPherson, KS)

Manpower Engineering

McPherson, Kansas, USA

Full-time

Our client, a leader in the environmental monitoring sector, is seeking an Environmental Monitoring Analyst to join their team. As an Environmental Monitoring Analyst, you will be part of a dedicated team supporting critical laboratory functions. The ideal candidate will have strong analytical skills, attention to detail, and a commitment to quality, which will align successfully with the organization's goals. Job Title: Environmental Monitoring Analyst - PM Shift (7pm - 7am) Scheduled 2,2,2,3 r

IT Field Technician

LabCorp

Newark, New Jersey, USA

Full-time

Labcorp is hiring an IT Field Technician. This person will travel daily to customer sites to provide support. This person should have a solid technical background troubleshooting hardware and software. At Labcorp we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development ca

Validation Engineer

Katalyst Healthcares and Lifesciences

Richmond, Virginia, USA

Full-time

Responsibilities: Ensure that all manufacturing equipment (e.g., mixers, conveyors, packaging lines) undergoes Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) to confirm that they function correctly and meet operational specifications. Validate manufacturing processes to ensure they are capable of consistently producing products that meet quality standards. This includes processes like blending, cutting, rolling, and packaging. Regularly revali

Senior Automation Engineer

Digitive LLC

Lansdale, Pennsylvania, USA

Contract, Third Party

Role: Senior Automation Engineer Location: Onsite (Lansdale, PA) Experience: 12+ Years Must Have's: Experience with having worked on DCS-MES Integration. PLC/ Robotics/ Automation systems. Life Sciences Manufacturing experience. Note: Looking for DeltaV automation experience. Also, Life Science Manufacturing batch experience is mandatory. Job Summary: The Senior Automation Engineer is responsible for developing, maintaining, and troubleshooting Control systems-MES integration solution in an in

Senior Mechanical Process Engineer (P.E.)

Jobot

Lenexa, Kansas, USA

Full-time

This Jobot Job is hosted by: Kurt Holzmuller Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $110,000 - $150,000 per year A bit about us: We are an award-winning (ENR), major North American firm that offers comprehensive services in real estate development, planning, architecture, engineering, and construction, consistently delivering complex projects on schedule and within budget. One of our specialized divisions focuses on expanding indust