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)
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
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.
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
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
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
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.
Job Title: QC Senior Scientist – Raw Materials Location: Portsmouth, NH (On-site) As a QC Scientist I, Raw Materials, you will support the testing and release of raw materials used in the manufacture of life-changing therapies.
California, US residents click here. The job details are as follows: Who We Are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purpose
QA Specialist II – Operations Location: Location: This position is based in our Portsmouth, NH office. This is a 1st shift position operating on a 12-hour rotating schedule (7:00 AM – 7:00 PM). The schedule follows
QA Specialist V – QA Inspection Audit Management 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
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
Role Description Job Description: This 2nd shift Team Leader in Fermentation is responsible for the safe execution of the Charles City production schedule in accordance with Good Manufacturing Practices and other applicable regulatory requirements. Team Leaders