Sterile Manufacturing Expert - Princeton - beBeeCompliance

We are seeking a dynamic Research Scientist to join our Process Integration & Design Research Group This person will significantly contribute to our technology strategy and help shape our roadmap in the field of advanced (including additive) manufacturing and sustainability. · Co ...

Develop and implement a new process for tracking WFH assets to improve efficiency, reporting, and auditing. Reconcile inventory reports by comparing system data with physical counts, resolving discrepancies, and preparing reconciliation summaries. · ...

We are seeking a Senior QC Specialist to support in-process and release testing for Cell and Gene Therapy (CGT) products. The Senior QC Specialist will also contribute to stability studies, microbiology, analytical, and reagent testing, delivering high-quality, on-time results to ...

Provide SAP Product Costing expertise for SAP components in the areas of: CO-PC, CO Sub modules, COPA. Learn and gain expert level knowledge of the Activity Based Costing/Basics Modules of the SAP Dairy Management Solution by msg and the SAP Meat and Fish Management Solution. · P ...

The Quality Operations Supervisor is a hands-on leadership role responsible for overseeing daily Quality Operations activities and ensuring compliance with cGMP and regulatory requirements across multiple sites. · Ensure site-wide GMP compliance and product quality. · Apply advan ...

We are seeking a dedicated Quality Specialist to join our dynamic team within a rapidly growing Cell and Gene Therapy CDMO at a brand new site. · Provide on-floor Quality Operations support for manufacturing, warehouse, and other technical operations, including in-process checks, ...

We are seeking a dedicated Quality Specialist to join our dynamic team within a rapidly growing Cell and Gene Therapy CDMO at a brand new site. · Provide on-floor Quality Operations support for manufacturing, warehouse, and other technical operations, including in-process checks, ...

We are seeking a dedicated Quality Specialist to join our dynamic team within a rapidly growing Cell and Gene Therapy CDMO at a brand new site. · Provide on-floor Quality Operations support for manufacturing, warehouse, and other technical operations, including in-process checks, ...

We are seeking a highly motivated Sr. / Engineer or Scientist to join our Process Development (PD) team at our Princeton location. This role will support hands-on process development, including optimization, troubleshooting, and tech transfer of client programs and technologies i ...

We are seeking a dedicated Quality Specialist to join our dynamic team within a rapidly growing Cell and Gene Therapy CDMO at a brand new site. · Provide on-floor Quality Operations support for manufacturing, warehouse, and other technical operations, including in-process checks, ...

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, our colleagues are challenging what's possible and making headway to innovate new treatment p ...

Responsible for batch certification review of site QA activities related to manufacturing batch records, packaging records and all related supporting documentation. Provides supporting role during regulatory, corporate and internal audits. · Supports Batch certification activitie ...

The Senior Validation Manager is leading the site validation program and all qualification and validation activities at the Erytech, Princeton site, NJ. · Define, implement and maintain the validation program for the site, ensuring compliance to the company quality guideline, FDA ...

The Quality Operations Supervisor is a hands-on leadership role responsible for overseeing daily Quality Operations activities and ensuring compliance with cGMP and regulatory requirements across multiple sites. · ...

The Quality Operations Supervisor is a hands-on leadership role responsible for overseeing daily Quality Operations activities and ensuring compliance with cGMP and regulatory requirements across multiple sites. · Ensure site-wide GMP compliance and product quality. · Apply advan ...

The Quality Operations Supervisor is a hands-on leadership role responsible for overseeing daily Quality Operations activities and ensuring compliance with cGMP and regulatory requirements across multiple sites. · ...

The Quality Operations Supervisor is a hands-on leadership role responsible for overseeing daily Quality Operations activities and ensuring compliance with cGMP and regulatory requirements across multiple sites. · Ensure site-wide GMP compliance and product quality. · Apply advan ...

The Manufacturing Support Associate is responsible for maintaining GMP readiness of scientific cleanrooms by executing routine and ad-hoc facility sanitization, performing both viable and non-viable environmental monitoring, and supporting material, equipment, and product flow th ...

The Manufacturing Associate III is responsible for advising and supporting the overall GMP manufacturing process, through the application of broad knowledge of theories and principles utilized to perform operational, as well as routine tasks in the production of cell therapy and/ ...

Provide SAP Product Costing expertise for SAP components in the areas of: CO-PC, CO Sub modules, COPA. Act as a Product Costing subject matter expert for the msg Food Business Unit in the Americas. · Provide guidance and recommendation to the clients · Support SAP Food Management ...

The Manufacturing Support Associate is responsible for maintaining GMP readiness of cleanrooms by executing routine and ad-hoc facility sanitization, performing viable and non-viable environmental monitoring, and supporting material/equipment/product flow throughout the facility. ...