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Cranford, NJ – Sr. PM BASIC FUNCTION: Coordinates and implements Clinical Trials projects.  Manages daily activities of established clinical trials. SCOPE OF SUPERVISION: N/A PRINCIPAL FUNCTIONAL RESPONSIBILITIES: Accountable for successful delivery of assigned clinical trials projects. Ensures that study specifications and deliverables are consistent with corporate and client expectations. Ensures that scope and timelines are clearly documented and agreed, according to client, protocol and internal ...

Project Manager – Cranford, NJ BASIC FUNCTION: Coordinates and implements Clinical Trials projects.  Manages daily activities of established clinical trials. SCOPE OF SUPERVISION: N/A PRINCIPAL FUNCTIONAL RESPONSIBILITIES: Accountable for successful delivery of assigned clinical trials projects. Ensures that study specifications and deliverables are consistent with corporate and client expectations. Ensures that scope and timelines are clearly documented and agreed, according to client, protocol and ...

 Our Large Global Pharmaceutical Client is looking for a Director of Quality to do the following: Ensures corporate compliance to Regulatory Agency requirements (i.e., FDA, EU, DEA, etc.) from a Quality perspective throughout the clients manufacturing plants within his oversight (and to some degree regarding contract manufacturing companies where this position acts as Quality liaison interact for limited third party cGMP oversight).  Head QA/QC Designee for US Operations within the Corporate CQMS ...

  · Assists in maintenance, quality control, distribution, and archiving of clinical documents and reports. · Supports development of program specific standards (e.g., agendas, minutes, filing structure, team materials). · Assists with the management and maintenance of team contact lists, calendars, and organizational charts. · Participates in meeting logistics, events and training, where requested by assigned program/compound leader(s), including (but not limited to) o Scheduling ...

Description This position supports our Home Appliance Division in the USA by providing an independent performance assessment. As team lead, the role of the consumer scientist is to coordinate and evaluate home appliances, such as ranges, MWO, refrigerators, laundry, dishwashers, vacuums, and AC, to specialized test conditions in order to determine our competitive edge, how to improve product, and document findings based on product performance using industry protocols. This also entails ...

Description: The Inventory Control and Distribution Technician will, with limited supervision: • Support Clinical Supplies projects in the areas of receiving, distribution, return, and destruction. • Receive product into inventory, coordinating inspection of incoming goods as appropriate. • Collaborate with Clinical Supplies Managers, the Clinical Supplies Floor Supervisor, and internal customers to achieve on-time delivery of clinical supplies that meet both project and regulatory requirements. ...

Description: The Clinical Supplies Label Control Coordinator will, with limited supervision: • Create and design labels for clinical supplies based on approved label text and appropriate product specifications and ensure approval of such by the appropriate personnel. • Produce and control printed labels for use in labeling operations. • Collaborate with Clinical Supplies Managers ,the Clinical Supplies Floor Supervisor, internal customers, and internal or external service providers to achieve on ...

Lead the development, implementation, and management of the GCP Quality program compliant with federal regulations (IRB and IEC) and company standards. Candidate must possess at least 5 years experience in the following: *** Developing and executing comprehensive annual audit plans for Clinical Trials. *** Planning, coordinating, and conducting internal and external audits. *** Overseeing Clinical Document Audits *** Writing, reviewing, and updating Standard Operating Procedures *** ...

JOB SUMMARY • Must complete all proper training forms for the applicable responsibilities listed below and contained within the position’s specific syllabus. • Must be a Team player able to effectively communicate with QA Supervisor, IPQA, Quality Control, Production, and Supply Chain to meet finished product release goals. • Be able to perform all IPQA (In-Process Quality Assurance) functions. • Be able to perform incoming and outgoing inspections of finished product batches. • Have 2-3 year ...

It is the formulator scientist responsibility to develop the batches as per current guidelines and to take trials for Development Batches, Scale up Batches and for Validation batches. Formulation Scientist is responsible for Bio- Batches and also to provide documentation for Regulatory purpose. It is responsibility of Formulation Scientist to ensure that the equipment’s used for e.g. Granulation, Blending, Compression, Coating and Packaging are clean and set up properly and the equipment’s are in ...

It is the Formulation Scientist responsibility to develop the batches as per current guidelines and to take trials for Development Batches, Scale up Batches and for Validation batches. Formulation Scientist is responsible for Bio- Batches and also to provide documentation for Regulatory purpose. It is responsibility of Formulation Scientist to ensure that the equipment’s used for e.g. Granulation, Blending, Compression, Coating and Packaging are clean and set up properly and the equipment’s are in ...