Business Analyst Role Business Analyst with strong TrackWise functional expertise to support and enhance Quality Management System (QMS) processes in a regulated Life Sciences environment. The role involves requirement analysis, stakeholder coordination, and ensuring successful delivery of
Job Title Pay Range: $83.88hr - $88.88hr Requirements/Must Have: Minimum 8 years of TrackWise System Analysis experience. Perform business requirements gathering, requirements analysis, business system design, installation, configuration, user testing and validation support of TrackWise based applications. Create
TrackWise Consultant Location: Short Hills, NJ (Onsite) Duration: C2C Contract Job Description: Strong SQL background with understanding of TrackWise data structure. Analyzes detailed business, functional and high-level technical requirements. Configuration and customization of TrackWise system. Trackwise, PL/SQL Strong verbal and
Technical Consultant Business Analyst with strong TrackWise functional expertise to support and enhance Quality Management System (QMS) processes in a regulated Life Sciences environment. The role involves requirement analysis, stakeholder coordination, and ensuring successful delivery of TrackWise-based solutions.
TrackWise Consultant Location: Fremont, CA preferred & Remote okay Mandatory Skills: Looking for a pure TrackWise Consultant (not generic QA/QMS) with strong workflow configuration + API integration + SQL backend expertise, and exposure to QMS processes (CAPA/NC/Change Control)
Associate Director, QA Ops Location: This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 8:00 AM–5:00 PM EST. What you will get: Below you will find a comprehensive
The Sr. Manager, Quality Systems -Audits & CAPAs is responsible for the day-to-day management and hands-on execution of CareTria’s internal audit, supplier audit, and Corrective and Preventive Action (CAPA) programs. This role manages the operational delivery
We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes
About fme Life Sciences: fme Life Sciences focuses on Business Solution deployments leveraging Enterprise Content Services platforms for clients in the Life Sciences Industry. fme Life Sciences is increasingly regarded as a trusted vendor and partner
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our
Position Summary Conducts activities within the Quality Control functions of Incoming Inspection of components and raw materials (ensuring that materials meet specifications), In-Process audits (ensuring that manufacturing operations remain in control), and the inspection and release
QMS Administrator Location: Tampa, FL Join our Tampa site as a QMS Administrator and play a key role in strengthening enterprise quality systems that support life-changing therapies. This is an exciting opportunity to contribute to digital
Description Execute activities associated with the Global PV processes for PV Computerized Systems Administration and Data Analysis. Monitor these processes to ensure continued compliance with all BIV PV SOPs and competent health authority regulations. Identify areas
Description This position has responsibility for key QA functions and the responsibility of training others to perform functions including but not limited to the coordination of documentation systems to ensure compliance, control, accountability, traceability, communication, retrieval
What we offer Explore a world of opportunities with us. Look ahead with us and help shape innovative solutions to make our world more sustainable and life healthier, more vibrant and more comfortable. At Evonik, you
This is what you will do: The Associate Director will lead the development, characterization, technology transfer, and validation of sterile injectable drug products across a range of modalities including biologics, peptides, nucleic acids, and synthetic molecules.
QC Analyst III, Analytical - Large Scale Allogenic Manufacturing Location: Portsmouth, NH, USA. Schedule: Monday - Friday, 8:00 AM-5:00 PM We are seeking an advanced laboratory professional to join our Quality organization in Portsmouth, NH, as
About Site Catalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting customers from research through early‑ and mid‑stage clinical production. Located at 726 Heartland Trail in Madison, the approximately 102,700‑square‑foot GMP facility
Manager - Manufacturing Sciences & Technology (Upstream Technology Transfer) Position Summary: Work Schedule: Monday – Friday, core hours 8am-5pm 100% on-site (Madison, WI) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located
Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering