e are looking for an experienced QC Incoming Associate with experience in regulated industries. Responsibilities: Managing retain samples of Raw Materials, Finished Goods and Bulk. Storing reserve samples under specified temperature and hum...
We are seeking a Senior Engineer with hands-on experience with technical assessments supporting FDA/regulatory commitments, manufacturing-floor investigations, root cause analysis, deviation investigations, and CAPA development and implemen...
Validation Specialist with a strong knowledge of injection molding processes to support the development, execution, and documentation of validation activities (Protocols, Tests, Reports). Familiarized with IQ, OQ and PQ validation phases fo...
We are seeking a Process Engineer with pharma-medical device experience as well as validations life-cycle experience (write/execute/analyze/close) to support the daily operations: Root cause analysis Investigation experience for QN/CAPAclos...
The Methods Transfer - Validation Specialist is responsible for planning, executing, and documenting analytical method transfers, validations, verifications, and method improvement initiatives in compliance with regulatory requirements. Thi...
Validation Specialist with experience in regulated industry to perform chemist laboratory equipment qualifications. Strong knowledge of generation of documents and equipment designs, working with equipment manuals, Data Integrity and Softwa...
We are seeking a Sr. Engineer who will provided and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environmen...
We are seeking a Quality Assurance Specialist to perform critical QA oversight activities, ensuring compliance with regulatory requirements, internal quality standards, and site procedures. This role requires the ability to work with minima...
We are seeking a Specialist QA. The responsibilities include: • Perform On-the-floor Plant Quality Assurance (PQA) review, approval, and tracking of cGMP processes, procedures, testing methods in manufacturing, documents and records, batch ...
We are looking for a qualified Validation Specialist with knowledge and experience with aseptic and regulated processes and developing and executing: Validation protocols. Validation reports. SOPs (Standard Operating Procedures). Statistica...