Trabajos biotech manufacturing en New Brunswick, New Jersey (NJ) State

Support the implementation of manufacturing and process improvement strategies through cell therapy manufacturing process design qualification, vendor evaluation, and enterprise system interface engineering support for GMP manufacturing of engineered autologous T cell therapy products. Legend Bio...

Associate Director, Manufacturing Operations Lead. The Associate Director, Manufacturing Operations Lead will be responsible for performing the activities necessary to start up and run a new in-house GMP facility and deliver Phase 1 clinical trial material for several cell therapy pipeline assets...

Contract Manufacturing Associate. Support Quality activities at Contract Manufacturing Organizations (CMO) by providing timely and effective quality oversight. Review of manufacturing and packaging records. Support significant quality issues associated with Drug Products or Medical Devices origin...

Must Have: Minimum of 4 years of relevant experience in Engineering and/or Quality or advanced degree in Engineering, Science, or technical fieldNice to Have:Audit Training (ISO 13485 and FDA 21CFR820Training)PLM Tools: AgileMap, Windchill, SAPPowerBIASQ CSQP and/or CQE Certificate CAPA Training....

Associate’s degree and completion of an accredited medical laboratory technician program is preferred. For Customer Service posting, performs essential duties related to reference lab test processing and resulting. One year clinical laboratory experience preferred (Student experience acceptable. ...

Perform appropriate Lab practices and procedures for making product formulation and testing of products. Maintain, monitor, validate and calibrate lab equipment, as necessary. Previous laboratory experience preferred. Must have hands-on experience with laboratory instruments. ...

Ordering raw materials, making batches and keeping track of experiments in lab notebook. ...

Conducts internal process benchmarking in partnership with process stakeholders to identify best-in-class solutions as well as areas to enhance performance, efficiency and productivityEnsure sustainability of all improvements post-implementation by partnering with cross-functional team leaders an...

Project Manager, Global Supply Chain. Experience in project/program management of complex projects involving cross-functional, multi-site, global teams. Lead and ensure successful deployment of strategic projects. Drive program/project activities, including kickoff meetings, recurring status meet...

The CClient Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. In parallel, the technical writer could help support non regulatory writing projects such as SOP and techni...

The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. In parallel, the technical writer could help support non regulatory writing projects such as SOP and technical ...

Must have experience in single-use pharmaceutical manufacturing. Support the preparation of solutions and buffers for manufacturing processes in accordance with relevant SOPs and/or master batch records, adhering to GMP standards. Familiarity with Downstream manufacturing, including depth filtrat...

Establish Project Plan via Microsoft Project. ...

The Manager, Global Clinical Operations (GCO) will be responsible for the direct functional management of a group Site Managers (SMs) in the Oncology Therapeutic Areas (TA) within GCO U. DescriptionJanssen Research & Development, LLC, is recruiting for a Functional Manager, Global Clinical Operat...

The Trial Manager - Medical Affairs Operations (MAO) will be accountable for leading the execution of local company data generation activities in one or more countries for project(s) assigned by the Global Program Leader (GPL), Functional Manager, or Operations Head. DescriptionJanssen Research &...

Seeking a Pharmaceutical Process Engineer with minimum of 7-15 years experience. Ideal candidates should have a strong understanding of GMPs and experience providing Project Engineering support in highly regulated or pharmaceutical facilities. Candidates should have demonstrated experience with m...

The Senior Quality Compliance Engineer will work with the Senior Manager of Quality Compliance to ensure Terumo Medical Corporation is achieving compliance to all global regulations and external standards for medical devices, combination medical device/pharmaceutical, and software products throug...

As a PT or FT Pepsi Warehouse Worker, you can take pride in knowing that you helped get Pepsi products to every corner of the world! Not to mention, you will embark on an incredible career journey - generous pay, Total Rewards benefits for you and your family (Health & Insurance, Well-being resou...

Go just about anywhere and you will find Pepsi products.As a Pepsi Stocker, you can take pride in knowing that you helped get Pepsi products to every corner of the world! Not to mention, you will embark on an incredible career journey - generous pay, Total Rewards benefits for you and your family...

We utilizes a motivated team of inhouse subject matter experts, construction managers, project managers, engineers, and project staff to manage the execution of the engineering, procurement, and construction of various projects. The Engineer will be required to apply principles, knowledge, and pr...

Project Manager with experience to join our expanding team. Excelling in all phases of construction for sewers, water/wastewater, Pump Stations and site development projects. Water and wastewater design projects experience. Pump station design and rehabilitation, collection system condition asses...

We are a specialized engineering company with international exposure and subject mater expertise in the design, fabrication and qualification of sterile, high purity and potent containment process equipment and plants. We offer a true creative engineering design work environment with a wide range...

The Manager, Global Clinical Operations (GCO) will be responsible for the direct functional management of a group Site Managers (SMs) in the Oncology Therapeutic Areas (TA) within GCO U. DescriptionJohnson & Johnson is currently seeking a Functional Manager, Global Clinical Operations - Oncology ...

Bachelor or Master’s Degree in General Engineering or ideally Aerospace Engineering. ...