- 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
- Astellas Pharma (Sanford, NC)
- ** Associate III, Downstream Manufacturing** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are ... please visit our website at www.astellas.com . **Purpose and Scope:** The Associate III, Downstream Manufacturing, will be a key contributor to manufacturing… more
- Abbott (Abbott Park, IL)
- …for manufacturing and research environment at Abbott Lake County. Requires adherence to quality and regulatory requirements (as referenced in GMP 's, SOP's, DEA, ... out of our Lake Bluff, IL location in the GES, Global Engineering Services. As a Housekeeping Associate , you will perform facility cleaning and support required… more
- Boehringer Ingelheim (Gainesville, GA)
- **Description** The SR Associate , Quality Control Data will manage the following functions in the Quality Control Department. This includes LIMS, Sample Life ... Cycle Management and Quality Control test documentation life cycle management in compliance with procedures and regulatory requirements. The incumbent will be… more
- US Tech Solutions (Thousand Oaks, CA)
- …performs routine laboratory testing and related activities in support of Quality Control operations. The role requires adherence to current Good Manufacturing ... laboratory procedures and analytical testing in a regulated QC environment + Document , calculate, compile, interpret, and enter laboratory data accurately and in a… more
- Fujifilm (Warminster, PA)
- **Position Overview** **Position Description** We are hiring an Associate Director, Quality Assurance. The Associate Director, Quality Assurance will ... program, internal and supplier audit programs, customer audit management, document control, quality control, batch releases, change...as a quality resource with expertise in quality regulations relating to GMP and ISO… more
- Lilly (Indianapolis, IN)
- …around the world. **Position Overview** Drug Product External Manufacturing (DPEM) Quality Assurance assures patients worldwide of safe and efficacious drug ... products, through effective quality oversight of North, Central and South American contract...packaging product. The QA Lead is integral for maintaining GMP compliance and providing support during preparations for Pre-Approval/… more
- BD (Becton, Dickinson and Company) (Columbus, NE)
- …Corrective and preventive action programs (CAPA) + GMP training initiatives + Quality engineering + Change control processes + Document control systems + ... **maker of possible** with us. We are seeking a dynamic and experienced ** Associate Director, Quality Management** to drive organizational change and grow within… more
- Fujifilm (Thousand Oaks, CA)
- …rooms and equipment + Perform tasks in a manner consistent with the safety policies, quality systems, and GMP requirements + Initiate Work orders as needed + ... **Position Overview** The Senior Manufacturing Associate works as part of the manufacturing team...tasks in a manner consistent with the safety policies, quality systems, and GMP requirements **Qualifications:** +… more
- Merck (Rahway, NJ)
- …Engineering Lead to support specialty dosage forms and oral solid dosage (OSD) GMP development activities on second shift. The successful incumbent will serve as the ... technical lead for shift production, coordinating safety, quality , and equipment decisions. This role evaluates safety,...next steps, including stop‑work when risk warrants; escalate and document per cGMP expectations. + Serve as owner and… more
- Edwards Lifesciences (Irvine, CA)
- …biotech, aerospace, automotive, or food industries. + Experience with supplier quality , change controls, document controls, change management systems, and/or ... Imagine how your ideas and expertise can change a patient's life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of… more