- Actalent (Shawnee Mission, KS)
- Quality Assurance Associate - GMP Document Control Key Responsibilities: + Maintain document control for GMP documents, ensuring accuracy and ... identify opportunities for process efficiencies. + Revise and route GMP documentation through the Document Management System...years of experience in document control or quality documentation within a GMP -regulated environment. Job… more
- Mentor Technical Group (Durham, NC)
- …+ Execute aseptic filling, compounding, and manufacturing processes in compliance with GMP and aseptic techniques. + Operate, monitor, and maintain equipment used in ... and sterilize equipment, components, and materials for aseptic operations. + Document activities accurately and completely in batch records, logbooks, and electronic… more
- Catalent Pharma Solutions (Philadelphia, PA)
- ** Quality Assurance Document Control** **Position Summary:** + **Work Schedule: Monday - Friday, 8:00am-4:30pm** + **100% on-site** Catalent's ... of a team that delivers industry-leading quality and innovation. The Quality Assurance Document Control role is responsible for preparing customer files,… more
- Charles River Laboratories (Rockville, MD)
- …build a career that you can feel passionate about. **Job Summary** The Associate Director Quality is responsible for partnering with functional stakeholders at ... of achievable solutions + Manages the walkthrough program in GMP Manufacturing, quality control testing, storage and...in other functional Quality areas such as Quality Systems, Training, Document Control, and Supplier… more
- Actalent (Bothell, WA)
- Description: The role is responsible for the administration of the document control, training and supplier quality processes within the electronic Quality ... including grammar, formatting, and consistency. Partner with stakeholders to ensure document effective dates align with quality requirements and timelines.… more
- Bristol Myers Squibb (Madison, NJ)
- …more: careers.bms.com/working-with-us . **Position Summary** Bristol-Myers Squibb is seeking an Associate Director, Principal Product Quality Leader (PQL), in ... and cell therapy projects) to ensure regulatory compliance of GMP operations in support of the program.The PQL must...should be directed to Chat with Ripley. R1597688 : Associate Director, Principal Product Quality Lead **Company:**… more
- Actalent (Waltham, MA)
- Job Title: Quality Assurance Associate Job Description We...crucial role in mitigating gaps and risks for all quality and GMP processes, and will run ... are seeking a dedicated Quality Assurance Associate to support on-the-floor QA issues within our manufacturing...manufacturing suite. + Mitigate gaps and risks for all quality and GMP processes. + Conduct investigations… more
- Amgen (Holly Springs, NC)
- …Join us and transform the lives of patients while transforming your career. **Senior Associate Quality Assurance - PQA** **What you will do** Let's do this. ... change the world. The Amgen North Carolina (ANC) Sr. Associate Plant Quality Assurance (PQA) on-the-floor position...will facilitate real-time decision making to ensure adherence to GMP quality requirements. This is a unique… more
- Actalent (Bothell, WA)
- …including grammar, formatting, and consistency. Partner with stakeholders to ensure document effective dates align with quality requirements and timelines. ... Description + Serve as the Document Coordinator for the document workflows...adoption. + Manage the distribution, tracking, and follow-up of GMP supplier questionnaires. + Liaise with material suppliers to… more
- Merck (Rahway, NJ)
- …Improvement position to support specialty dosage forms and oral solid dosage GMP development activities. This role is primarily responsible for compliance and ... continuous improvement activities including safety, quality , delivery and continuous improvement within clinical supply Formulation Laboratory and Experimentation… more