We are seeking a Senior Associate to join the Issue Validation Team within Internal Audit. This is an exciting opportunity to join a dynamic and agile team where members learn from each other and grow together to
Job Description The Director, Business Systems Validation External / Automation provides strategic leadership and direction to validation teams within an assigned geography. They oversee performance management, organizational capability building and process optimization. They partner with other leaders on
Job Title: Senior Scientist Location: Cherry Hill NJ Job Type: Fulltime About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ purpose is to put better health within
Computer System Validation Specialist Computer System Validation, CSV, GxP, 21 CFR part 11, Risk Based Approach Roles and Responsibilities 10+ yrs. of experience in Computer System Validation Senior Level individual with GxP experience Ability to lead, fully knowledgeable of
Manager of DRG Coding & Clinical Validation Audit Manager of DRG Coding Audit-Program/Project Locations: The selected candidate must reside within a reasonable commuting distance of the designated posting location(s): Virginia, Indiana, Georgia, Ohio, Maryland; New Jersey, New
Validation Lead Raritan, NJ OR New Brunswick, NJ (Onsite Hybrid Model ( 3 days a week) ) Long Term Contract Job Responsibility: Must be able to work out of Raritan or New Brunswick Office at least 3
Validation Analyst We are seeking a Validation Analyst to support validation of our Quality Management System (MasterControl) and SAP implementation (QM, Materials Management, Production modules). This role works under the direction of a senior validation lead and partners with Quality,
Manager, IT Validation Services Working with Us Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day,
Lead Validation Engineer The Lead Validation Engineer leads GMP equipment installation, commissioning, and qualification projects supporting large-molecule biologics manufacturing. This role supports upstream and downstream processes and ensures projects are executed safely, on schedule, and in compliance with
Validation Lead (Computer System Validation GenAI, Agentic QMS) Location: Raritan, NJ (Hybrid) $50/hr on w2 Experience in the pharmaceutical, biotechnology, or medical device industry 2+ years experience with System Development Lifecyle 3+ years experience in Computer System Validation Experience
Payroll - Validation Professional Location: 126 E. Lincoln Avenue Rahway, NJ Qualifications: Education: Bachelors Degree with a minimum of 8+yrs of applicable experience Required: Knowledge of ADP Technology ev6, Workday, MS Office Candidate would need to be
Senior Quality Validation Specialist We are seeking an innovative and highly motivated Senior Quality Validation Specialist, who will contribute significantly to the growth of the Cellares team. The Quality Validation team at our IDMO Bridgewater facility will be responsible
Job Title Pay Range: $48hr - $53hr Requirements/Must Have Experience in the pharmaceutical, biotechnology, or medical device industry. 2+ years experience with system development lifecycle. 3+ years experience in computer system validation. Experience in FDA and/or global
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
Validation Lead Mandatory Skills: CSV/ Compliance and Assurance services/ Validation Testing/ Audit Management/ CAPA and Deviation/ Pharma GxP/ Biopharma and Medical devices/ GAMP5, GxP, 21 CFR Part 11 and Annex 11 compliance Job Qualifications - Validation Lead: Must have
Director, Business Systems Validation External / Automation The Director, Business Systems Validation External / Automation provides strategic leadership and direction to validation teams within an assigned geography. They oversee performance management, organizational capability building and process optimization. They partner
Project Manager Our project managers are technical leads first, with a strong background in CQV strategy, development, and field execution. We look for culture fit above all our people are our most important asset, and great
Project Manager, Validation You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work that is
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
Validation Lab Manager The Validation Lab Manager will manage a team of technicians supporting ZT Systems Validation Engineering group on several projects in various stages of development. The Lab Manager will plan and manage the physical hosting of validation racks