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
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)
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
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Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer
Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer
Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer
Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day,
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
Description As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally,
We are seeking a detail-oriented and operationally rigorous Quality Control Raw Material Analyst to join our Quality Control (QC) team in Bridgewater, New Jersey. The primary focus of this position is to support raw material incoming
Description To be a technical subject matter expert in assessing instrument calibrations as compared to engineering/user requirements, provide hands on and/or formal training for calibration, engineering, and end users as needed.As an employee of Boehringer Ingelheim,
Manufacturing Project Specialist Houston, TX The actual location of this job is in Houston, TX, US. Relocation assistance is available for eligible candidates and their families, if needed. This is a fully site‑based role. Working together
McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the
Description Employee assigned to QC functional or technical area in either HPLC/CE, Potency testing (Bioassay and Binding assays), Residual Impurities, Physicochemical/Drug Product, Raw Materials/Cleaning validation/verification. Performs duties under limited supervision and according to standard operating and
Job Description The GMP Operational Quality Sr. Manager is an advanced technical resource in the principles and application of quality assurance and compliance. The Sr. Quality Manager coordinates or executes activities on multiple complex projects and
Specialist I, Quality Assurance Position Summary: Work Schedule: M-F 8am-5pm 100% on-site Working for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making significant investments in people and capabilities. This is
Hillsboro Technical Operations (HTO) is a drug product & finished goods manufacturing organization responsible for the reliable delivery of Roche’s commercial portfolio & pipeline products. The Manufacturing organization at HTO is divided into two groups, Aseptic
Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know youve got big plans - so do we! Our colleagues across the globe love