The CSV Consultant will be responsible for supporting Computer System Validation (CSV) activities across GMP laboratory and manufacturing environments at Somerset, New Jersey site reporting to CSV Manager. The role includes execution of validation lifecycle deliverables, implementation of data
Responsibilities The Senior Specialist, IT Compliance & Validation is responsible for ensuring that FDA-regulated computerized systems, as well as other critical enterprise systems are validated, controlled, and maintained in compliance with applicable regulatory requirements, including 21 CFR Part 11, 21
Responsibilities The Senior Specialist, IT Compliance & Validation is responsible for ensuring that FDA-regulated computerized systems, as well as other critical enterprise systems are validated, controlled, and maintained in compliance with applicable regulatory requirements, including 21 CFR Part 11, 21
Responsibilities The Senior Specialist, IT Compliance & Validation is responsible for ensuring that FDA-regulated computerized systems, as well as other critical enterprise systems are validated, controlled, and maintained in compliance with applicable regulatory requirements, including 21 CFR Part 11, 21
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
SHIFT: Sunday-Thursday (11PM - 7AM) The Mechanic 1 Technician will work in conjunction with the maintenance, production, and engineering departments. The primary job responsibility is to support production through effective and timely equipment downtime troubleshooting involving
TITLE Registration Processing Specialist I JOB SUMMARY Performs registration processing in support of student, faculty, administrative and campus community progress. Responsibilities include providing customer service to students, faculty and staff, answering phone inquiries, advising students on
Job Description: Job Title: Certified Peer Specialist Location: Independence, Missouri Department: Recovery Services Employment Type: Full Time Shift: Tuesday-Saturday 8am-5pm Job Summary: Are you a passionate and dedicated mental health professional looking to make a positive
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Medical Assistant II- Riley Pediatric Primary Care North/Carmel Location: 14828 Greyhound Court, Suite 100 Carmel, IN 46032 Schedule Full-time Alternating shifts: 7:00 AM – 4:00 PM 8:00 AM – 5:00 PM Occasional weekend shifts available (optional,
Medical Assistant II - Full-Time/Days/40 hours per week Location: Carmel, IN (11725 N Illinois St, Suite 140) Monday–Friday | 7:45 AM – 4:15 PM No weekends or observed holidays What You’ll Do Room patients and assist
Advanced Medical Laboratory Technician The Advanced Medical Laboratory Technician position is assigned to P&LMS at Central Arkansas Veterans Healthcare System (CAVHS) Medical Center, Little Rock, Arkansas. They perform a variety of waived, moderate, and complex tests on
Select how often (in days) to receive an alert: QA Validation & Equipment Compliance Manager Date: May 30, 2026 Department: Quality Operations Italy, Parma Site Job Type: Direct Employee Business Area: Quality Contract Type: Permanent Location: Parma,
Experteer Overview In this role, you provide quality oversight for qualification and validation activities, ensuring regulatory compliance and data integrity across GMP manufacturing. You will lead the site Validation Program and oversee CSV governance to guarantee products meet
Global Technical Operations & Supply Global TechOp&S is Chiesi’s global manufacturing and supply area, responsible for ensuring consistent, outstanding quality, service and value across our end‑to‑end supply chain. Global TechOp&S oversees the entire lifecycle of the
Responsibilities Accountable for driving achievement of project milestones from study start‑up through to delivery of the database and monitoring of time spent on tasks. Provide Database Programming input into protocol data collection assessments. Create the annotated
Principal Database Programmer role at Alira Health Job Description Summary The Principal Database Programmer will lead and mentor the database programming team, ensuring high‑quality clinical databases that adhere to industry standards and project requirements. Role Characteristics
Experteer Overview As Principal Database Programmer, you lead the Database Programming (DBP) team and shape the clinical database to capture study data from paper and electronic CRFs. You develop data checks (SAS and otherwise), ensuring accurate,