- Aequor (Thousand Oaks, CA)
- …include evaluation of compliance issues, providing recommendations, and assuring progress of quality records to completion. The Sr. Associate will also represent ... experience is more important. Candidates should be familiar with manufacturing or quality operations and understand the pace and expectations of a high-volume,… more
- Aequor (West Greenwich, RI)
- …preferred.Basic Qualifications: Science related background, lab experience Bachelor's degree OR Associate 's degree and 4 years of experience OR High school diploma ... / GED and 6 years of experience more
- Aequor (Thousand Oaks, CA)
- …or GED and two years of relevant work or military experience, though an associate 's degree with six months of experience is also acceptable. A bachelor's degree is ... sampling and inspection of raw materials and components and for performing Quality review of documentation for assigned functions (eg equipment and maintenance… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionDevice Development Associate Principal Scientist - Development Strategy, Design Controls( Associate Director Equivalent) Our company's Device ... medical device and healthcare regulations, including FDA combination products cGMP, Quality System Regulation, FDA Human Factors guidance, ISO 14971, EN 62366,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …organizations, and study investigators- Manage vendor budget and activities- Oversee the quality and timeline of vendor work- Collaborate with study clinical or ... the planning, execution and delivery of publication projects to ensure high quality and timely delivery of scientific publications- Manage publication activities in… more
- Aequor (Pearl River, LA)
- …manufacturing equipment under close supervision in accordance with current relevant quality standards or standardized procedures and within safety guidelines in the ... etc. Interacts with other departmental personnel to assist in resolving manufacturing quality issues. Technician should have the ability to manage and analyze… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …your potential? The Position The Active Pharmaceutical Ingredient (API) Planning Associate will support completion of planning activities and PAS-X/SAP related ... projects. He/she will work with Planners, Manufacturing, Facilities, Quality Control, MSAT, and Engineering to support and improve the planning processes across the… more
- Repligen (Hopkinton, IA)
- OverviewWe are seeking a Document Control/QA Associate I to join our growing Quality Department team in Hopkinton, MA for 1st shift operations (M-F) from 8 am ... EST - 4:30 pm EST.The Document Control/QA Associate I will report directly to the QA/QC Director.This...responsible to actively participate in the Repligen ISO 9001 Quality Management System. This role is responsible for assisting… more
- Merck & Co. (San Francisco, CA)
- Job Description Position Description: Associate Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) ... modalities. We are interdependent across our functional areas, Discovery, our Manufacturing Division Quality , and BARDS, to name a few, and with our partners in… more
- Twist BioScience (South San Francisco, CA)
- …our Twist Bioscience Operations Team in South San Francisco. The Manufacturing Associate , will perform basic molecular biology workflows in a highly automated, ... (7:00am-7:30pm)Roles and Responsibilities include but are not limited to:Manufacture high quality custom products in a high throughput MFG lab according to… more
- Insmed Incorporated (San Diego, CA)
- …lead on a PDT as required by the business.ResponsibilitiesThe Analytical Development Operations associate director is responsible for building a team to take care of ... trend analysis are also key duties. Collaboration with R&D, Process Development, Quality Control, and Regulatory Affairs is essential, as is facilitating technology… more
- Merck & Co. (North Wales, PA)
- …that project plans are executed efficiently with timely and high quality deliverables.For assigned projects the position serves as the statistical programming ... in CDISC and ADaM standardsDemonstrated success in the assurance of deliverable quality and process compliance.Strategic thinking - ability to turn strategy into… more
- Merck & Co. (Rahway, NJ)
- …in Rahway, New Jersey.The Sterile Process Engineer role at the Associate Director level will leverage the individual's leadership, technical, and communication ... and process development through process tech transfer, scale-up activities, quality investigations, change management, and authoring GMP standard operating… more
- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionGRACS CMC - Associate Principal Scientist, CMC, R4 - Pharm Pre-approval Reporting to the Sr Director/Director/Principal Scientist/Sr Principal ... pharmaceutical operations (eg, manufacturing, formulation and process development, analytical, quality assurance, n ovel modality and technologies such as synthetic… more
- AUROBINDO (Durham, NC)
- …family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality control and regulatory affairs. In addition ... to several formulations under manufacture, we have a robust pipeline of products. Aurolife's aim is to provide healthcare at economical prices to make this a healthier world to live in.Job OverviewDedicated, knowledgeable, responsible/ reliable employee who… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a Warehouse Operations Associate III as part of the Technical Operations team based in Raritan, NJ. ... space. This individual will assist in regulatory inspections, perform safety and quality audits, and answer relevant questions about packaging, methods, storage, and… more
- Eisai, Inc (Exton, PA)
- … Quality Control, Regulatory, and CMC Program Management departments.The Associate Director of Biologics Operations maintains knowledge of established and ... difference. If this is your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible for leading and… more
- Merck & Co. (Rahway, NJ)
- …a lead GCS Planning program representative ) such as clinical development, regulatory, quality and other supply chain areas to negotiate timelines ,- strategies and ... software . - Familiarity with Good Manufacturing Practices (GMP) requirements, quality procedures, and Standard Operating Procedure (SOP) execution. - - #MSJR… more
- Merck & Co. (Durham, NC)
- …the Master Data team with general Material Handling Steward tasksDrive safety, quality and process enhancements throughout the supply chain - Project Management Lead ... and sponsor all Supply Chain Logistics initiatives surrounding qualification support of off-site warehouse facilities for ambient and -70 storage capacity needs and flammable storage facility constructionCreation and updating of all associated standard… more
- Aequor (Walkersville, MD)
- …finishing activities Assisting in reviewing paperwork and logbooks for the department Quality Responsibility Maintenance of quality systems and cGMP compliance ... for the business by ensuring that all team members comply with processes, procedures and instructions for all activities in which the team participates. Safety Responsibility Is knowledgeable and complies with all pertinent safety policies, rules and… more
