Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. Every member of
Title: SAP Batch Release Hub SME Location: Philadelphia, PA (Hybrid- 2 days in a week) Duration: 8 Months Job Responsibilities: Lead SAP Batch Release Hub (BRH) solution design and sustainment activities for Life Sciences clients, translating business, quality, manufacturing, and
Lead SAP Batch Release Hub (BRH) Consultant Location: Philadelphia, PA (Hybrid role 1-2 days onsite) Duration 6-12 Months Must understand GMP/GxP, FDA regulations, 21 CFR Part 11, validation documentation, audit readiness, and batch release processes. Prior MedTech, Pharma, Biotech, or
Description: The Mixing operator is responsible for operation of the Mixing and Granulation equipment in accordance with Company Standard Operating Procedures and maintaining 100% cGMP & compliance to ensure the production of quality products. Schedule: 1st
Overview Job Title: Sr AS400 DeveloperLocation: Hybrid - King of Prussia, PA (4 days onsite/1 day remote) Job Type: Independent Contract (Contractor / Non-Employee)Start Date: ASAP Pay Rate: $60-65/hr 1099 / C2C Contract Length: 12+ Months
This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week No relocation is provided for this opportunity Who We Are: At West, we’re a dedicated team that
Description: The QA Inspector monitors and ensures all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. The QA Inspector must
Director, Quality Position Summary: 100% on-site Catalent’s 206,878-square-foot Philadelphia-area facility serves as the global Center of Excellence for Clinical Supply Packaging, offering GMP secondary packaging and clinical labeling services. The site provides manual to fully automated
Quality Assurance Document Control Position Summary Work Schedule: Monday – Friday, 4:00pm-12:30am. 100% on-site Catalent’s 206,878-square-foot Philadelphia-area facility serves as the global Center of Excellence for Clinical Supply Packaging, offering GMP secondary packaging and clinical labeling
Job FamilyIT - Development About Us At Transamerica, hard work, innovative thinking, and personal accountability are qualities we honor and reward. We understand the potential of leveraging the talents of a diverse workforce. We embrace an
Job FamilyIT - Development About Us At Transamerica, hard work, innovative thinking, and personal accountability are qualities we honor and reward. We understand the potential of leveraging the talents of a diverse workforce. We embrace an
We are passionate about our employees. We strive to create an environment that is stimulating and motivating and a culture that fosters mutual respect, teamwork, and career development. Come join the Keystone team so we can
Description: Entry Level Role in the Mixing department. The Mixing operator is responsible for operation of the Mixing and Granulation equipment in accordance with Company Standard Operating Procedures and maintaining 100% cGMP & compliance to ensure
VP Of Global IT QA The VP of Global IT QA will provide leadership, strategy & direction with an overall accountability for IT Quality Assurance teams across all Centralized QA functions. This includes overseeing multiple teams
Sr. Manager, Packaging Project Management Head Pharmacy Biotech Job Description This position manages the Great Valley site Packaging Project Management group. This is comprised of Clinical Supplies Packaging Managers (CSPM) and the Packaging Instructions group. CSPM
VP Quality, Global Life Sciences As VP Quality, Global Life Sciences you will be accountable for the enterprise quality vision, strategy, and operating model across Ecolabs Life Sciences business globally, including Bioprocessing, Purification Technologies, and Pharma
Director, Quality Catalents 206,878-square-foot Philadelphia-area facility serves as the global Center of Excellence for Clinical Supply Packaging, offering GMP secondary packaging and clinical labeling services. The site provides manual to fully automated packaging solutions, including temperature-controlled
PCI Pharma Services Join us and be part of building the bridge between life changing therapies and patients. Lets talk future Our investment is in People who make an impact, drive progress and create a better
PCI Pharma Services Job Opportunity Join us and be part of building the bridge between life changing therapies and patients. Lets talk future Our investment is in People who make an impact, drive progress and create
Quality Management Role at Cardinal Health Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications. Quality Management provides strategic oversight, leadership and direction within the