- Sanofi Group (Swiftwater, PA)
- …technical solutions and communicating outcomes to site management. + Review/approve process design specifications, technical documents, validation project plans ... related to the Continuous Improvement of Packaging for Drug Products and process monitor program. As an individual contributor within the organization, the role… more
- Kelly Services (Irvine, CA)
- …seeking an experienced R&D Director for a full-time position with a leading pharmaceutical client located in Irvine, CA. This role is perfect for someone passionate ... letters. + **Protocol Management** : Write and review method validation /development protocols/reports. + **Research & Investigation** : Conduct research and… more
- Actalent (Skokie, IL)
- …II, you will perform microbiological environmental monitoring in a pharmaceutical manufacturing clean room environment. You will conduct microbiological analysis, ... monitoring and sampling within manufacturing areas. + Sample, test, review, and verify process utilities such as nitrogen, compressed air, pure steam, and WFI. +… more
- Lilly (Indianapolis, IN)
- …reference materials. Develop, verify, quality, and validate methods to support in- process , release, characterization analysis and stability testing of active ... pharmaceutical ingredient and drug products. Introduce new methodologies for...of: 5 years of experience with overseeing analytical method validation protocols and validation reports; 5 years… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …is well-positioned to successfully emerge as a leading integrated research-based pharmaceutical company. POSITION SUMMARY: + Microbiologist ll/lll is responsible for ... include routine and non-routine microbiological tests and investigative testing on in- process and final container products, as well as environmental monitoring… more
- Eurofins (Lancaster, PA)
- …is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation ... the generation of protocols, methods or reports + Draft, review and author validation protocols, methods and reports, with support, as appropriate + With the support… more
- Cambrex High Point (Longmont, CO)
- …work. * Knowledge of global GMP and regulatory requirements related to the pharmaceutical drug development / manufacturing process . * Communicate clearly and ... needs. * Recruits, trains, develops, and retains staff for the effective process of departmental operations. * Effectively resolves quality issues and concerns in… more
- AbbVie (North Chicago, IL)
- …agency regulations worldwide. Products include regulatory starting materials, Active Pharmaceutical Ingredients (API), Intermediates, and Drug Products produced by ... and improved Quality systems within Operations. Influences the decision making process to ensure quality requirements are included when improvement initiatives take… more
- Bayer (Morristown, NJ)
- …analysis, or a related field; + Hands-on knowledge in method development and validation of pharmaceutical tests (Assay, Impurities, Dissolution); + Knowledge of ... execute analytical experiments of medium complexity, focusing on method development, validation , and transfer to manufacturing sites/CMOs. Your expertise will ensure… more
- Fresenius Medical Center (Waltham, MA)
- …+ Manages the end-to-end preparation, compilation, publishing, quality control, validation , and delivery of electronic regulatory submissions (eCTD) in compliance ... within MS Word and Adobe Acrobat, and supports resolution of validation errors. + Participates in evaluating and implementing new regulatory technologies;… more