- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …(eg SOP-s, Specifications, Standard Test Procedures, Test Data Sheet, Method transfer/ validation protocols/ reports and QMS records, Investigations, etc. + Assists ... + Provide guidance and work with stakeholders from various departments to process Quality control documentation, internal and external audit + Provide required… more
- Mentor Technical Group (Juncos, PR)
- …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... Communication skills Project Management + Knowledge in Computer System and Method Validation (Experience preferable) + Strong knowledge and experience with quality … more
- Teva Pharmaceuticals (Davie, FL)
- …be contributing to the prototyping, design, analysis, modeling, verification and validation for simple robotics systems. From rapid prototyping to detailed ... experience and projects (preferred projects linked to material handling and pharmaceutical of food manufacturing) + Strong understanding of mechanical or electrical… more
- WuXi AppTec (Middletown, DE)
- …high quality standards are maintained and appropriate documentation such as process design, commissioning, qualification, and validation documentation is ... platform standardization and uniformity, establish global guidelines in pharmaceutical DS/DP R&D and manufacturing facility design/construction/C&Q process .… more
- Lilly (Philadelphia, PA)
- …Quality Control (AD/QC) is responsible for managing the development and validation of phase-appropriate methods for radiopharmaceutical imaging agents throughout the ... and development. **Key Responsibilities:** + Manage the development and validation of phase-appropriate (pre-clinical through commercial) analytical methods to… more
- Jabil (Hunt Valley, MD)
- …in a clear and concise manner. They will work together with the validation scientists to ensure accuracy of protocols and reports by following Standard Operating ... on-site position involves preparing scientific documents in collaboration with R&D validation scientists. The technical writer prepares and finalizes validation ,… more
- Abbott (San Diego, CA)
- …actively participate in product development and transfer activities, ensuring product and process conformance to FDA and ISO 13485 standards. This position will ... review validation methods and protocols, test methods, statistical analysis methods...FDA and applicable non-US regulations pertaining to medical or pharmaceutical manufacturing, including hardware, software, and bioassay systems. **EDUCATION… more
- Teleflex (Morrisville, NC)
- …Morrisville. A core responsibility of this role is leading Test Method Validation (TMV) and analytical method transfer activities consistent with FDA, ICH (Q2/Q14), ... AND 3+ years of experience in a regulated analytical laboratory environment (medical device, pharmaceutical , or equivalent); or * MS degree in a related field AND 2+… more
- Eurofins US Network (Winston Salem, NC)
- …causes, and applies process improvements + Provides analysis support for method validation as needed + Evaluates, reviews, and approves data by other analysts + ... of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract...needed + Assists in Method Development and executes method validation protocols + Assist in method transfer from the… more
- AbbVie (Worcester, MA)
- …size process lines, equipment, and instrumentation. Support commissioning and validation of project related equipment, facility, and/or utilities to ensure the ... gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie AbbVie Co-Ops. Under the… more
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