Process & Validation Project Manager Location: Philadelphia, PA Employment Type: Full-time, mostly onsite About Us Are you ready to take the next step in your career? LAPORTE, a consulting engineering firm with 25 years of experience and a
Veolia is seeking a Senior Process Engineer to join the Technical Direction and Process Validation team in the United States. The role involves evaluating opportunities, developing PFDs/P&IDs, and supporting Sales and Commercial Engineering with process expertise. You will lead design
Company Description Veolia Group is a global leader in environmental services, operating across all five continents with nearly 218,000 employees. Specializing in water, energy, and waste management, Veolia Group designs and implements innovative solutions for decarbonization,
Our client, a highly respected U.S.-based specialty chemical manufacturer with more than 60 years of industry leadership, has created a new Sr Process Technology Engineer - High Pressure Processing position at their Pennsylvania headquarters. In this highly
Senior Clinical Computer System Validation Engineer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and
Job Title: Process Supervisor - 2nd Shift (Monday to Friday, 3:00PM to 11:30PM) Location: Cherry Hill, New Jersey Job Type: Full-time Description: We continue to be committed to building a diverse and inclusive team and encourage applications
Audit Manager I Work Location: New York, New York, United States of America Hours: 40 Pay Details: $75,020 - $125,180 USD TD is committed to providing fair and equitable compensation opportunities to all colleagues. Growth opportunities
Utilization Management & Clinical Validation Rn Optum is a global organization that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes
PCI Pharma Services Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes
Audit Manager II The Audit Manager II provides specialized expertise to help guide the planning, risk assessment, and execution of audits. This role plays an essential part in shaping the strategic direction of the audit function,
Validation Sme - Delivery Leader East Coast (Multiple) Veristas 500 experts team up with the worlds most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower
Manager AI Assisted Process, Risks and Controls Transformation Our Deloitte Regulatory, Risk & Forensic team helps client leaders translate multifaceted risk and an evolving regulatory environment into defensible actions that strengthen, protect, and transform their organization. Join
Audit Manager II Work Location: New York, New York, United States of America Hours: 40 Pay Details: $92,220 - $149,310 USD TD is committed to providing fair and equitable compensation opportunities to all colleagues. Growth opportunities
Audit Manager I Issue Validation (Insider Risk/Internal Fraud) Work Location: New York, New York, United States of America Hours: 40 Pay Details: $75,020 - $125,180 USD TD is committed to providing fair and equitable compensation opportunities to
Process Development & Efficacy (PDE) Manager The Clinical Cell and Vaccine Production Facility (CVPF) and Center for Advanced Cellular Therapies (CACT) of the University of Pennsylvania manufacture advanced cell and gene therapy products in support of pioneering
Validation Manager The Validation Manager leads the end-to-end planning, coordination, and execution of a portfolio of site projects focused on process and product validation, product and technology transfer, and validation and qualification workstreams. This role partners closely with cross-functional stakeholders to
Job Title Job Description: 12 years experience in validating systems and experienced in GxP related applications. Perform review for GxP systems to ensure compliance with regulatory requirements as per the customer SOPs. Expertise on end-to-end validation of
Job Title 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
Description The Company: This publicly held clinical-stage biotechnology company is focused on developing treatments for patients suffering from complex rare diseases using its novel cell penetrating peptide technology platform. Their lead product candidate, nomlabofusp, is a
Company Description Veolia Group is a global leader in environmental services, operating across all five continents with nearly 218,000 employees. Specializing in water, energy, and waste management, Veolia Group designs and implements innovative solutions for decarbonization,