Responsibilities: Develop global regulatory strategies for medical device products to meet business objectives and collaborate across a matrixed organization to ensure global success of products\' registration. Participate in product de...
Responsibilities: We are seeking experienced CQV (Commissioning, Qualification, and Validation) Engineers with a strong pharmaceutical background to join our team in Pennington, NJ. The ideal candidate must be ready to work fully onsite...
Responsibilities: Act as Lead Data Manager, overseeing all deliverables of activities outsourced to DM CRO for multiple studies. Interact and manage relationships with other functional areas to ensure high quality data management activi...
Coordinate with the India Engineering Center (IEC) and enable successful project execution and have a daily sync with the offshore team and IEC leadership Perform a full lifecycle product development (Design, Develop, test prototypes, and ...
Responsibilities & Requirements: Expert Skills- Computer System Validation. Validating ERP to AWS Data migration process. Validating Data migration project. Experience in the Pharmaceutical, biotechnology, or medical device industry...
Responsibilities : Partner with lab scientists and technicians, engineers, IT, QAU and vendors in managing and/overseeing the completion of qualification and validation activities associated with installation, maintenance, and upgrades of...
Responsibilities: The Regulatory Affairs Manager is responsible for the development and execution of global regulatory strategy and tactical planning for assigned microbiology on market products or those products in development. Assures...
Responsibilities: Develop global regulatory strategies for medical device products to meet business objectives and collaborates across a matrixed organization to ensure global success of products registration. Participate on product dev...
Summary: Research and test the design, functionality and maintenance of products, equipment, systems and processes and develop quality standards. Ability to read and interpret blueprints, and evaluate product integrity and standards. Typica...
Responsibilities: Maintains all qualified and validated equipment and systems in compliance with policies, guidelines, and procedures. Support Lifecycle Document Management System. Develops protocols, and associated reports while adheri...
Responsibilities: We are seeking experienced CQV (Commissioning, Qualification, and Validation) Engineers with a strong pharmaceutical background to join our team in Pennington, NJ. The ideal candidate must be ready to work fully onsite...
Responsibilities and Requirements: Must have knowledge and experience with GMP, Quality and compliance. Previous experience as a computer system validation / quality assurance for life sciences company regulated by the FDA is preferred. ...
Responsibilities & Requirements: Client is looking for a consultant who specializes in MES & LIMS sample management module as well as help with a QMS update. The QMS update has no specific timeline .(done by end of year) Tulip is MES an...
Responsibilities: Partner with client Commercial Sales and Marketing, Market Access, Commercial Operations, and other stakeholders to implement Veeva CRM and related technology solutions in alignment with key business priorities. Config...
Responsibilities and Requirements: The candidate will work as a Manufacturing Design Engineer, responsible for reviewing and modifying drawings/blueprints to ensure accuracy and design feasibility. They will also create flat layout desig...
Responsibilities: Independently support data maintenance and archival and retrieval of regulatory documentation in computerized systems. Assist with preparing high quality US regulatory submissions required by local and federal agencies ...
Responsibilities: This position has primary responsibility for investigation, review, and completion of all Quality Engineering complaint issue analysis tasks utilizing various quality system inputs. Review individual complaints and asso...
Responsibilities and Requirements: Seeking Supply Chain Planner skilled in Project management to support Client Brand Transition program. Drive global supply chain project management of supply planning activities to implement previous Cl...
Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs act...
Responsibilities: Looking for an R statistical programmer/analyst to support a small biotech. There is not a computing environment set up yet so the person will use the RStudio desktop app and leverage R (like R Shiny) for data visualizat...